PROF Profound Medical Corporation

Indicate by check mark whether the registrant files or will file annual reports under cover of Form 20-F or Form 40-F.
Form 20-F [   ]      Form 40-F [ X ]

Exhibits 99.2 and 99.3 of this Form 6-K are incorporated by reference into Profound Medical Corp.’s registration statement on Form F-10 (File No. 333-263248).

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EXHIBIT INDEX

The following document is attached as an exhibit hereto and is incorporated by reference herein:  

Exhibit		Title
99.1		Press Release dated August 8, 2024
99.2		Unaudited Interim Condensed Consolidated Financial Statements
99.3		Management’s Discussion and Analysis
99.4		Form 52 - 109F2 - Certification of Interim Filings - CEO
99.5		Form 52 - 109F2 - Certification of Interim Filings - CFO

 

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SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.

		PROFOUND MEDICAL CORP.
		(Registrant)
Date: August 8, 2024		/s/ Rashed Dewan
		Rashed Dewan
		Chief Financial Officer

EXHIBIT 99.1

Profound Medical Announces Second Quarter 2024 Financial Results

TORONTO, Aug. 08, 2024 (GLOBE NEWSWIRE) -- Profound Medical Corp. (NASDAQ:PROF; TSX:PRN) (“Profound” or the “Company”), a commercial-stage medical device company that develops and markets customizable, incision-free therapies for the ablation of diseased tissue, today reported financial results for the second quarter ended June 30, 2024. Unless specified otherwise, all amounts in this press release are expressed in U.S. dollars and are presented in accordance with International Financial Reporting Standards as issued by the International Accounting Standards Board.

Business Highlights

• The TULSA-PRO^® systems installed base grew from 53 at the end of Q1-2024 to 57 as of the end of Q2-2024; Profound continues to expect that to grow to 75 TULSA-PRO^® systems this year.
• Profound continued to see a wide variety of prostate disease patients treated by its TULSA-PRO^® customers in the second quarter of 2024:
  • 73% were treated for prostate cancer, 15% were hybrid patients suffering from both prostate cancer and benign prostatic hyperplasia (“BPH”), 8% were salvage, and 4% were men with BPH only;
  • For cancer grade, 5% were GG1, 50% were GG2, 34% were GG3, and 11% were GG4 & GG5;
  • In terms of ablation, 50% were whole gland; 29% were sub-total but more than half the gland; and 21% were hemi-ablations or focal therapy; and
• For prostate size, 6% were < 20cc; 45% were 20 – 40cc; 30% were 40-60cc; 12% were 60-100cc; and 7% were over 100cc.
• In May 2024, Profound received U.S. Food and Drug Administration (“FDA”) clearance for its second TULSA-AI module, Contouring Assistant, a machine learning-based prostate segmentation tool designed to assist in efficiently delineating the prostate and target patient volume. The Company continues to develop its third TULSA-AI module, TULSA-BPH, for use in conjunction with the TULSA-PRO^® system and expects to provide additional details on that later this year.
• In July 2024, the U.S. Centers for Medicare & Medicaid Services (CMS) issued its proposed outpatient prospective payment system (OPPS) reimbursement rule for the three new CPT^® Category 1 codes and their descriptors covering the TULSA procedure, with the final rule anticipated in November 2024, which will become effective on January 1, 2025.
• The ongoing Level 1 CAPTAIN trial comparing the TULSA procedure to radical prostatectomy in men with localized prostate cancer remains on track to complete patient enrollment by the end of this year, and Profound anticipates beginning to report interim data from this post-market study in the first half of 2025.
  

“While we continue to make strong commercial progress, in some ways we are just approaching the starting line as we make final preparations for the permanent CPT^® Category 1 codes for TULSA going into effect at the beginning of 2025, an anticipated major inflection point for our business,” said Arun Menawat, Profound’s CEO and Chairman. “Adequate reimbursement is generally considered essential for treatment technology innovators like Profound to drive forward widespread adoption and, importantly, we believe CMS’ proposed rule for TULSA will put us on at least a level playing field with competing current standard-of-care and other prostate disease treatment modalities.”

Second Quarter 2024 Results

For the quarter ended June 30, 2024, the Company recorded revenue of $2.23 million, with $1.46 million from recurring revenue, which consists of the sale of TULSA-PRO^® consumables, lease of medical devices, procedures and services associated with extended warranties, and $773,000 for one-time sale of capital equipment. Second quarter 2024 revenue increased 39% from $1.60 million in the same three-month period a year ago.

Total operating expenses, which consist of research and development (“R&D”), general and administrative (“G&A”), and selling and distribution (“S&D”) expenses, were $9.3 million in the second quarter of 2024, an increase of 24% compared with $7.5 million in the second quarter of 2023.

Expenditures for R&D for the three months ended June 30, 2024 were $4.2 million, an increase of 33% compared with $3.2 million in the three months ended June 30, 2023, primarily due to various R&D projects undertaken during the period, which included fixture developments, yield improvements and additional materials for clinical trials, higher headcount and lower reimbursement of workforce costs. Partially offsetting these amounts was a decrease in share-based compensation due to fewer awards granted to employees.

G&A expenses for the 2024 second quarter were $2.1 million, essentially unchanged from the same period in 2023. Salaries and benefits increased due to higher cost of living salary increases. Partially offsetting this was a decrease to insurance expense due to lower premium rates and a decrease to general office expenses.

Second quarter 2024 S&D expenses increased by 32% to $3.0 million, compared with $2.3 million in the second quarter of 2023. This was driven by increases in salaries and benefits, consulting fees and travel due to increased salesforce and commission payments, consultants engaged to assist with Veteran Affairs and military sales markets, and increased in-person conferences and customer meetings.

Net finance income for the three months ended June 30, 2024 was $934,000, compared with net finance expense of $884,000 in the three months ended June 30, 2023.

Second quarter 2024 net loss was $6.9 million, or $0.28 per common share, compared to $7.3 million, or $0.35 per common share, in the three months ended June 30, 2023.

Current 2024 Outlook

As previously disclosed, based on the Company’s current business planning and budgeting activities, Profound anticipates its total revenue for full-year 2024 to be in the range of $11.0 million to $12.0 million, representing total year-over-year revenue growth of 53% to 67%.

Liquidity and Outstanding Share Capital

As at June 30, 2024, Profound had cash of $34.1 million.

As at August 8, 2024, Profound had 24,481,835 common shares issued and outstanding.

For complete financial results, please see Profound’s filings at www.sedarplus.ca, www.sec.gov and on the Company’s website at www.profoundmedical.com under “Financial” in the Investors section.

Conference Call Details

Profound Medical is pleased to invite all interested parties to participate in a conference call today at 4:30 pm ET during which time the results will be discussed.

To participate in the conference call by telephone, please pre-register via this link to receive the dial-in number and your unique PIN.

The call will also be broadcast live and archived on the Company's website at www.profoundmedical.com under "Webcasts" in the Investors section.

About Profound Medical Corp.

Profound is a commercial-stage medical device company that develops and markets customizable, incision-free therapies for the ablation of diseased tissue.

Profound is commercializing TULSA-PRO^®, a technology that combines real-time MRI, robotically-driven transurethral ultrasound and closed-loop temperature feedback control. TULSA-PRO^® is designed to provide customizable and predictable radiation-free ablation of a surgeon-defined prostate volume while actively protecting the urethra and rectum to help preserve the patient’s natural functional abilities. TULSA-PRO^® has the potential to be a flexible technology in customizable prostate ablation, including intermediate stage cancer, localized radio-recurrent cancer, retention and hematuria palliation in locally advanced prostate cancer, and the transition zone in large volume benign prostatic hyperplasia (“BPH”). TULSA-PRO^® is CE marked, Health Canada approved, and 510(k) cleared by the U.S. Food and Drug Administration (“FDA”).

Profound is also commercializing Sonalleve^®, an innovative therapeutic platform that is CE marked for the treatment of uterine fibroids and palliative pain treatment of bone metastases. Sonalleve^® has also been approved by the China National Medical Products Administration for the non-invasive treatment of uterine fibroids and has FDA approval under a Humanitarian Device Exemption for the treatment of osteoid osteoma. The Company is in the early stages of exploring additional potential treatment markets for Sonalleve^® where the technology has been shown to have clinical application, such as non-invasive ablation of abdominal cancers and hyperthermia for cancer therapy.

Forward-Looking Statements

This release includes forward-looking statements regarding Profound and its business which may include, but is not limited to, any express or implied statements regarding current or future financial performance and position, including the Company’s year 2024 financial outlook and related assumptions; the expectations regarding the efficacy of Profound’s technology in the treatment of prostate cancer, BPH, uterine fibroids, palliative pain treatment and osteoid osteoma; and its future revenues/financial results. Often, but not always, forward-looking statements can be identified by the use of words such as "plans", "is expected", "expects", "scheduled", "intends", "contemplates", "anticipates", "believes", "proposes" or variations (including negative variations) of such words and phrases, or state that certain actions, events or results "may", "could", "would", "might" or "will" be taken, occur or be achieved. Such statements are based on the current expectations of the management of Profound. The forward-looking events and circumstances discussed in this release, may not occur by certain specified dates or at all and could differ materially as a result of known and unknown risk factors and uncertainties affecting the Company, including risks regarding the medical device industry, regulatory approvals, reimbursement, economic factors, the equity markets generally and risks associated with growth and competition, statements and projections regarding financial guidance and goals and the attainment of such goals may differ from actual results based on market factors and Profound’s ability to execute its operational and budget plans; and actual financial results may not be consistent with expectations, including that revenue, operating expenses and cash usage may not be within management's expected ranges. For additional risks, please see the Company’s annual information form for the year ended December 31, 2023 and other disclosure documents available on www.sedarplus.ca and www.sec.gov. Although Profound has attempted to identify important factors that could cause actual actions, events or results to differ materially from those described in forward-looking statements, there may be other factors that cause actions, events or results to differ from those anticipated, estimated or intended. No forward-looking statement can be guaranteed. Except as required by applicable securities laws, forward-looking statements speak only as of the date on which they are made and Profound undertakes no obligation to publicly update or revise any forward-looking statement, whether as a result of new information, future events, or otherwise, other than as required by law.

Financial Outlook

This press release contains a financial outlook within the meaning of applicable securities laws. The financial outlook has been prepared by management of the Company to provide an outlook for the Company’s forecasted revenue for the 12 months to be ended December 31, 2024 and may not be appropriate for any other purpose. The financial outlook has been prepared based on a number of assumptions including the assumptions discussed under the heading “Forward-Looking Statements” herein. The actual results of the Company’s operations for any period may vary from the amounts set forth in these projections and such variations may be material. The Company and its management believe that the financial outlook has been prepared on a reasonable basis. However, because this information is highly subjective and subject to numerous risks, including the risks discussed under the heading “Forward-Looking Statements” herein, it should not be relied on as necessarily indicative of future results.

For further information, please contact:
Stephen Kilmer
Investor Relations
skilmer@profoundmedical.com
T: 647.872.4849

Profound Medical Corp.
Interim Condensed Consolidated Balance Sheets
(Unaudited)

	June 30, 2024 $			December 31, 2023 $
Assets
Current assets
Cash	34,079			26,213
Trade and other receivables	7,162			7,288
Inventory	6,732			6,989
Prepaid expenses and deposits	517			1,406
Total current assets	48,490			41,896
Property and equipment	680			909
Intangible assets	374			490
Right-of-use assets	488			616
Total assets	50,032			43,911
Liabilities
Current liabilities
Accounts payable and accrued liabilities	2,671			3,282
Deferred revenue	676			721
Long-term debt	2,024			2,104
Lease liability	258			259
Total current liabilities	5,629			6,366
Deferred tax liability	59			59
Long-term debt	3,943			5,000
Deferred revenue	735			728
Lease liability	427			578
Total liabilities	10,793			12,731
Shareholders’ Equity
Share capital	230,842			217,393
Contributed surplus	20,138			19,687
Accumulated other comprehensive income	19,308			12,031
Deficit	(231,049	)		(217,931	)
Total Shareholders’ Equity	39,239			31,180
Total Liabilities and Shareholders’ Equity	50,032			43,911

Profound Medical Corp.
Interim Condensed Consolidated Statements of Loss and Comprehensive Loss
(Unaudited)

	Three months ended June 30, 2024 $			Three months ended June 30, 2023 $		Six months ended June 30, 2024 $			Six months ended June 30, 2023 $
Revenue
Recurring - non-capital	1,460			1,602		2,942			3,069
Capital equipment	773			-		1,201			393
	2,233			1,602		4,143			3,462
Cost of sales	795			552		1,436			1,199
Gross profit	1,438			1,050		2,707			2,263
Operating expenses
Research and development	4,193			3,155		8,126			6,995
General and administrative	2,109			2,080		4,496			4,186
Selling and distribution	2,969			2,251		5,400			4,356
Total operating expenses	9,271			7,486		18,022			15,537
Operating loss	7,833			6,436		15,315			13,274
Net finance expense/(income)	(934	)		884		(2,256	)		739
Loss before income taxes	6,899			7,320		13,059			14,013
Income taxes expense	20			35		59			83
Net loss attributed to shareholders for the period	6,919			7,355		13,118			14,096
Other comprehensive (income)/loss
Item that may be reclassified to loss
Foreign currency translation adjustment- net of tax	(2,068	)		4,117		(7,277	)		4,164
Net loss and comprehensive loss for the period	4,851			11,472		5,841			18,260
Loss per share
Basic and diluted loss per common share	0.28			0.35		0.54			0.67

Profound Medical Corp.
Interim Condensed Consolidated Statements of Cash Flows
(Unaudited)

	Six months ended June 30, 2024 $		Six months ended June 30, 2023 $
Operating activities
Net loss for the period	(13,118	)	(14,096	)
Adjustments to reconcile net loss to net cash flows from operating activities:
Depreciation of property and equipment	383		351
Amortization of intangible assets	101		101
Depreciation of right-of-use assets	108		108
Share-based compensation	1,535		1,783
Interest and accretion expense	339		384
Deferred revenue	18		142
Change in fair value of derivative financial instrument	-		232
Net change in amortized cost of trade and other receivables	(168	)	(79	)
Changes in non-cash working capital balances
Trade and other receivables	13		(27	)
Prepaid expenses and deposits	859		465
Inventory	(168	)	(191	)
Accounts payable and accrued liabilities	(508	)	334
Income taxes payable	2		16
Foreign exchange on cash	(844	)	(465	)
Net cash flow used in operating activities	(11,448	)	(10,942	)
Financing activities
Issuance of common shares	22,938		-
Transactions costs paid	(1,859	)	-
Payment of long-term debt	(1,227	)	(372	)
Proceeds from share options exercised	1		239
Proceeds from warrants exercised	-		2,423
Payment of lease liability	(145	)	(146	)
Total cash flow from financing activities	19,708		2,144
Net change in cash during the period	8,260		(8,798	)
Foreign exchange on cash	(394	)	1,556
Cash – Beginning of period	26,213		46,517
Cash – End of period	34,079		39,275

Exhibit 99.2

 

 

PROFOUND MEDICAL CORP.

 

 

 

 

 

INTERIM CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

 

JUNE 30, 2024

 

PRESENTED IN US DOLLARS (000s)

 

 

 

 

 

 

 

 

 

 

 

 

 

Profound Medical Corp.

Interim Condensed Consolidated Balance Sheets

In USD (000s)

(Unaudited)

 

		June 30, 2024 $				December 31, 2023 $
Assets
Current assets
Cash			34,079				26,213
Trade and other receivables (note 3)			7,162				7,288
Inventory (note 4)			6,732				6,989
Prepaid expenses and deposits			517				1,406
Total current assets			48,490				41,896
Property and equipment (note 5)			680				909
Intangible assets (note 6)			374				490
Right-of-use assets (note 7)			488				616
Total assets			50,032				43,911
Liabilities
Current liabilities
Accounts payable and accrued liabilities			2,671				3,282
Deferred revenue			676				721
Long-term debt (note 8)			2,024				2,104
Lease liability (note 9)			258				259
Total current liabilities			5,629				6,366
Deferred tax liability			59				59
Long-term debt (note 8)			3,943				5,000
Deferred revenue			735				728
Lease liability (note 9)			427				578
Total liabilities			10,793				12,731
Shareholders’ Equity
Share capital (note 10)			230,842				217,393
Contributed surplus			20,138				19,687
Accumulated other comprehensive income			19,308				12,031
Deficit			(231,049	)			(217,931	)
Total Shareholders’ Equity			39,239				31,180
Total Liabilities and Shareholders’ Equity			50,032				43,911

 

The accompanying notes are an integral part of these interim condensed consolidated financial statements.

 

 

 

Profound Medical Corp.

Interim Condensed Consolidated Statements of Loss and Comprehensive Loss

In USD (000s)

(Unaudited)

 

		Three months ended June 30, 2024 $				Three months ended June 30, 2023 $				Six months ended June 30, 2024 $				Six months ended June 30, 2023 $
Revenue (note 12)
Recurring - non-capital			1,460				1,602				2,942				3,069
Capital equipment			773				-				1,201				393
			2,233				1,602				4,143				3,462
Cost of sales (note 13)			795				552				1,436				1,199
Gross profit			1,438				1,050				2,707				2,263
Operating expenses (note 13)
Research and development			4,193				3,155				8,126				6,995
General and administrative			2,109				2,080				4,496				4,186
Selling and distribution			2,969				2,251				5,400				4,356
Total operating expenses			9,271				7,486				18,022				15,537
Operating loss			7,833				6,436				15,315				13,274
Net finance expense/(income) (note 14)			(934	)			884				(2,256	)			739
Loss before income taxes			6,899				7,320				13,059				14,013
Income taxes expense			20				35				59				83
Net loss attributed to shareholders for the period			6,919				7,355				13,118				14,096
Other comprehensive (income)/loss
Item that may be reclassified to loss
Foreign currency translation adjustment- net of tax			(2,068	)			4,117				(7,277	)			4,164
Net loss and comprehensive loss for the period			4,851				11,472				5,841				18,260
Loss per share (note 15)
Basic and diluted loss per common share			0.28				0.35				0.54				0.67

 

The accompanying notes are an integral part of these interim condensed consolidated financial statements.

 

 

 

Profound Medical Corp.

Interim Condensed Consolidated Statements of Changes in Shareholders’ Equity

In USD (000s)

(Unaudited)

 

		Number of shares				Share capital $				Contributed surplus $				Accumulated other comprehensive income $				Deficit $				Total $
Balance – January 1, 2023			20,879,497				205,825				18,704				16,837				(189,362	)			52,004
Net loss for the period			-				-				-				-				(14,096	)			(14,096	)
Cumulative translation adjustment – net of tax of $nil			-				4,849				273				(4,164	)			-				958
Exercise of share options			32,851				392				(153	)			-				-				239
Exercise of warrants			285,138				4,223				(986	)			-				-				3,237
Vesting of RSUs			53,109				668				(668	)			-				-				-
Vesting of DSUs			10,000				135				(135	)			-				-				-
Change in terms of DSUs			-				-				241				-				-				241
Share-based compensation (note 11)			-				-				1,783				-				-				1,783
Balance – June 30, 2023			21,260,595				216,092				19,059				12,673				(203,458	)			44,366
Balance – January 1, 2024			21,370,565				217,393				19,687				12,031				(217,931	)			31,180
Net loss for the period			-				-				-				-				(13,118	)			(13,118	)
Cumulative translation adjustment – net of tax of $nil			-				(8,044	)			(670	)			7,277				-				(1,437	)
Shares issued in public offering and private placement (note 10)			3,058,334				21,079				-				-				-				21,079
Exercise of share options			101				1				(1	)			-				-				-
Vesting of RSUs			52,835				413				(413	)			-				-				-
Share-based compensation (note 11)			-				-				1,535				-				-				1,535
Balance – June 30, 2024			24,481,835				230,842				20,138				19,308				(231,049	)			39,239

 

The accompanying notes are an integral part of these interim condensed consolidated financial statements.

 

 

Profound Medical Corp.

Interim Condensed Consolidated Statements of Cash Flows

In USD (000s)

(Unaudited)

 

		Six months ended June 30, 2024 $				Six months ended June 30, 2023 $
Operating activities
Net loss for the period			(13,118	)			(14,096	)
Adjustments to reconcile net loss to net cash flows from operating activities:
Depreciation of property and equipment (note 5)			383				351
Amortization of intangible assets (note 6)			101				101
Depreciation of right-of-use assets (note 7)			108				108
Share-based compensation (note 11)			1,535				1,783
Interest and accretion expense (note 14)			339				384
Deferred revenue			18				142
Change in fair value of derivative financial instrument (note 14)			-				232
Net change in amortized cost of trade and other receivables (note 3)			(168	)			(79	)
Changes in non-cash working capital balances
Trade and other receivables			13				(27	)
Prepaid expenses and deposits			859				465
Inventory			(168	)			(191	)
Accounts payable and accrued liabilities			(508	)			334
Income taxes payable			2				16
Foreign exchange on cash			(844	)			(465	)
Net cash flow used in operating activities			(11,448	)			(10,942	)
Financing activities
Issuance of common shares (note 10)			22,938				-
Transactions costs paid (note 10)			(1,859	)			-
Payment of long-term debt (note 8)			(1,227	)			(372	)
Proceeds from share options exercised			1				239
Proceeds from warrants exercised			-				2,423
Payment of lease liability (note 9)			(145	)			(146	)
Total cash flow from financing activities			19,708				2,144
Net change in cash during the period			8,260				(8,798	)
Foreign exchange on cash			(394	)			1,556
Cash – Beginning of period			26,213				46,517
Cash – End of period			34,079				39,275
Supplemental cash flow information:
Interest paid, included in financing activities			307				320
Income taxes paid, included in operating activities			174				22

 

The accompanying notes are an integral part of these interim condensed consolidated financial statements.

 

 

1

Description of business

 

Profound Medical Corp. (Profound) and its subsidiaries (together, the Company) were incorporated under the Ontario Business Corporations Act on July 16, 2014. The Company is a medical technology company developing treatments to ablate the prostate gland, uterine fibroids, osteoid osteoma and nerves for palliative pain relief for patients with metastatic bone disease.

 

The Company’s registered address is 2400 Skymark Avenue, Unit 6, Mississauga, Ontario, Canada, L4W 5K5.

 

2

Summary of material accounting policies and basis of preparation

 

Basis of preparation

 

The Company prepares its consolidated financial statements in accordance with International Financial Reporting Standards as issued by the International Accounting Standards Board (IFRS Accounting Standards), applicable to the preparation of interim condensed consolidated financial statements, including International Accounting Standards (IAS) 34, Interim Financial Reporting. These interim condensed consolidated financial statements are presented in US dollars and should be read in conjunction with the Company’s annual financial statements for the year ended December 31, 2023, which were prepared in accordance with IFRS Accounting Standards.

 

These interim condensed consolidated financial statements are prepared in accordance with the accounting policies as set out in the Company’s annual consolidated financial statements for the year ended December 31, 2023. The presentation of these interim condensed consolidated financial statements is consistent with the presentation of the annual consolidated financial statements. The Board of Directors approved these consolidated financial statements on August 8, 2024. These consolidated financial statements comply with IFRS Accounting Standards.

 

The interim condensed consolidated financial statements were prepared on a going concern basis under the historical cost convention. The fair values of cash, trade and other receivables, accounts payable and accrued liabilities and lease liability approximate their carrying values, due to their relatively short periods to maturity. The fair value of the long-term debt approximates its carrying amount as it has a floating interest rate.

 

Accounting standards adopted during the year

 

Beginning on January 1, 2024, the Company adopted certain IFRS Accounting Standards and amendments:

 

·

Classification of liabilities as current or non-current (Amendments to IAS1)

·

Non-current liabilities with covenants (Amendments to IAS1).

 

The adoption of these amendments did not have a material impact on the interim condensed consolidated financial statements.

 

 

Accounting pronouncements issued but not yet effective

 

The IASB has issued classification, measurement and disclosure amendments to IFRS 9, Financial Instruments and IFRS 7, Financial Instruments: Disclosures with an effective date for annual reporting periods beginning on or after January 1, 2026. The amendments clarify the date of recognition and derecognition of some financial assets and liabilities and introduce a new exception for some financial liabilities settled through an electronic payment system. Other changes include a clarification of the requirements when assessing whether a financial asset meets the solely payments of principal and interest criteria and new disclosures for certain instruments with contractual terms that can change cash flows (including instruments where cash flows changes are linked to environment, social or governance targets).

 

IFRS 18, Presentation and Disclosure in Financial Statements (IFRS 18) is a new standard that will provide new presentation and disclosure requirements and which will replace IAS 1, Presentation of Financial Statements (IAS 1). IFRS 18 introduces changes to the structure of the income statement; provides required disclosures in financial statements for certain profit or loss performance measures that are reported outside an entity’s financial statements; and provides enhanced principles on aggregation and disaggregation in financial statements. Many other existing principles in IAS 1 have been maintained. IFRS 18 is effective for years beginning on or after January 1, 2027.

 

The adoption of these pronouncements are currently being assessed.

 

 

3

Trade and other receivables

 

The trade and other receivables balance comprises the following:

 

		June 30, 2024 $				December 31, 2023 $
Trade receivables, gross			6,961				7,145
Loss allowance			(75	)			(76	)
Less amortized cost adjustment			(138	)			(315	)
Trade receivables, net			6,748				6,754
Tax receivables			210				414
Other receivables			204				120
Total trade and other receivables			7,162				7,288

 

The Company applies the simplified approach to provide for expected credit losses prescribed by IFRS 9, which permits the use of the lifetime expected loss provision for all trade receivables. Trade receivables past due represents amounts not collected beyond the customer’s contractual terms. At June 30, 2024 there were $746 of trade receivables that were past due (December 31, 2023 - $648).

 

Management continually reviews the future cash flows used in the calculation of the amortized cost of its trade and other receivables. Due to access to customer locations, certain gross trade receivables totalling $3,425 are expected to have a longer repayment term due to the payment term being based on installation of the device. The Company recognized $99 and $168 of interest income for the three and six months ended June 30, 2024, respectively, $40 and $79 of interest income for the three and six months ended June 30, 2023).

 

 

4

Inventory

 

		June 30, 2024 $				December 31, 2023 $
Finished goods			4,398				4,646
Raw materials			2,356				2,351
Inventory provision			(22	)			(8	)
Total inventory			6,732				6,989

 

During the three and six months ended June 30, 2024, $751 and $1,274, respectively (three and six months ended June 30, 2023, $507 and $983) of inventory was recognized in cost of sales. The Company increased its inventory provision by $7 and $14 during the three and six months ended June 30, 2024 (decreased its inventory provision by $4 during the three months ended June 30, 2023 and increased its inventory provision by $2 during the six months ended June 30, 2023). There were no other inventory write-downs charged to cost of sales during the period ended June 30, 2024.

 

5

Property and equipment

 

		Leasehold improvements $				Equipment under lease $				Total $
At January 1, 2024
Cost			542				2,583				3,125
Accumulated depreciation			(384	)			(1,832	)			(2,216	)
Net book value			158				751				909
Six months ended June 30, 2024
Opening net book value			158				751				909
Additions			-				159				159
Foreign exchange			1				(6	)			(5	)
Depreciation			(28	)			(355	)			(383	)
Closing net book value			131				549				680
At June 30, 2024
Cost			542				2,742				3,284
Accumulated depreciation			(411	)			(2,193	)			(2,604	)
Net book value			131				549				680

 

 

 

6

Intangible assets

 

		Exclusive licence agreement $				Software $				Proprietary technology $				Brand $				Total $
As at January 1, 2024
Cost			231				978				3,456				681				5,346
Accumulated amortization			(114	)			(605	)			(3,456	)			(681	)			(4,856	)
Net book value			117				373				-				-				490
Six months ended June 30, 2024
Opening net book value			117				373				-				-				490
Foreign exchange			(3	)			(12	)			-				-				(15	)
Amortization			(10	)			(91	)			-				-				(101	)
Closing net book value			104				270				-				-				374
As at June 30, 2024
Cost			231				978				3,456				681				5,346
Accumulated amortization			(127	)			(708	)			(3,456	)			(681	)			(4,972	)
Net book value			104				270				-				-				374

 

7

Right-of-use assets

 

		Leased premises $
As at January 1, 2024
Cost			1,679
Accumulated depreciation			(1,063	)
Net book value			616
Six months ended June 30, 2024
Opening net book value			616
Foreign exchange			(20	)
Depreciation			(108	)
Closing net book value			488
As at June 30, 2024
Cost			1,679
Accumulated depreciation			(1,191	)
Net book value			488

 

The Company leases office premises in Mississauga, Canada. The lease agreement ends on September 30, 2026 with the rights to extend for another 5 years, which is not reasonably certain.

 

8

Long-term debt

 

On November 3, 2022, the Company signed a term loan agreement with CIBC Innovation Banking (CIBC) to provide a secured loan for total gross proceeds of C$10,000 maturing on November 3, 2027 with an interest rate based on prime plus 2% (CIBC Loan). The Company was required to make interest only payments until October 31, 2023 and monthly repayments of C$208 plus accrued interest commenced on October 31, 2023. All obligations of the Company under the CIBC Loan are guaranteed by current and future subsidiaries of the Company and include security of first priority interests in the assets of the Company and its subsidiaries. Initially, the Company had financial covenants in relation to the CIBC loan where unrestricted cash is at all times greater than EBITDA for the most recent six-month period, reported on a monthly basis and that revenue for any fiscal quarter must be 15% greater than revenue for the same fiscal quarter in the prior fiscal year, reported on a quarterly basis.

 

 

On September 26, 2023 an amendment to the CIBC Loan resulted in a change to the financial covenants. The amended covenants are that unrestricted cash must at all times be greater of: (i) to the extent EBITDA is negative for such period, EBITDA for the most recent nine-month period or (ii) $7,500, reported on a monthly basis; and that recurring revenue for any fiscal quarter must be 15% greater than recurring revenue for the same fiscal quarter in the prior fiscal year, reported on a quarterly basis. On March 31, 2024, the Company was in breach of the second covenant whereby revenue for any fiscal quarter must be 15% greater than revenue for the same fiscal quarter in the prior fiscal year. The Company received a waiver from CIBC in relation to this covenant breach.

 

On May 3, 2024, a second amendment to the CIBC Loan resulted in another change to the financial covenants. The amended covenants are that the recurring revenue covenant shall not be tested for any fiscal quarter in the 2024 fiscal year so long as unrestricted cash is no less than 2.5 multiplied by the principal amount of outstanding CIBC Loan at all times. The Company is in compliance with these financial covenants as at June 30, 2024.

 

		June 30, 2024 $				December 31, 2023 $
Balance - Beginning of period			7,104				7,174
Interest and accretion expense			323				727
Foreign exchange			(233	)			115
Repayment			(1,227	)			(912	)
Balance - End of period			5,967				7,104
Less: Current portion			2,024				2,104
Long-term portion			3,943				5,000

 

9

Lease liability

 

		June 30, 2024 $				December 31, 2023 $
Balance – Beginning of Period			837				1,056
Repayments			(145	)			(292	)
Foreign exchange			(23	)			30
Interest and accretion expense			16				43
Balance – End of Period			685				837
Less: Current portion			258				259
Long-term portion			427				578

 

 

10

Share capital

 

Common shares

 

The Company is authorized to issue an unlimited number of common shares.

 

Issued and outstanding (with no par value)

 

		June 30, 2024 $				December 31, 2023 $
24,481,835 (December 31, 2023 – 21,370,565) common shares			230,842				217,393

 

On January 2, 2024, the Company closed a public offering, resulting in the issuance of 2,666,667 common shares at a price of $7.50, for gross proceeds of $20,000 ($18,238, net of transaction costs). On January 16, 2024, the Company closed a non-brokered private placement, resulting in the issuance of 391,667 common shares at a price of $7.50, for gross proceeds of $2,938 ($2,841, net of transaction costs).

 

11

Share-based payments

 

Share options

 

Compensation expense related to share options for the three and six months ended June 30, 2024 was $129 and $298, respectively (three and six months ended June 30, 2023 was $293 and $708). A summary of the share option changes during the period presented and the total number of share options outstanding as at those dates are set forth below:

 

		Number of options				Weighted average exercise price C$
Balance - January 1, 2024			1,474,809				16.19
Granted			28,700				11.24
Exercised			(101	)			8.57
Forfeited/expired			(22,000	)			17.74
Balance - June 30, 2024			1,481,408				16.07

 

The Company estimated the fair value of the share options granted during the period using the Black-Scholes option pricing model with the weighted average assumptions below:

 

		March 18, 2024
Exercise price			C$11.24
Expected volatility			70	%
Expected life of options			6 years
Risk-free interest rate			3.54	%
Dividend yield			-
Number of share options issued			28,700

 

 

The following table summarizes information about the share options outstanding as at June 30, 2024:

 

Exercise price C$		Number of options outstanding				Weighted average remaining contractual life (years)				Number of options exercisable
8.01 – 10.00			316,508				4.80				313,998
10.01 – 12.00			138,234				4.97				109,534
12.01 – 14.00			34,150				7.34				12,511
14.01 – 16.00			140,956				2.88				135,648
16.01 – 18.00			418,989				5.90				418,989
18.01 – 20.00			11,450				8.96				2,862
20.01 – 22.00			300				6.13				287
22.01 – 24.00			409,321				6.88				316,487
24.01 – 26.00			1,500				6.38				1,337
28.01 – 30.00			10,000				6.70				8,130
			1,481,408				5.36				1,319,783

 

Long-term incentive plan

 

Share-based compensation expense related to long-term incentive plan (LTIP) for the three and six months ended June 30, 2024 was $639 and $1,237, respectively (three and six months ended June 30, 2023 was $549 and $1,075, respectively).

 

A summary of the RSU changes during the year are set forth below:

 

		Number of RSUs				Weighted average remaining contractual life (years)
Balance - January 1, 2024			493,396				1.99
Granted			30,000				2.92
Vested			(52,835	)			-
Forfeited			(11,666	)			-
Balance - June 30, 2024			458,895				1.75

  

A summary of the DSU changes during the period are set forth below:

 

		Number of DSUs
Balance - January 1, 2024 & June 30, 2024			75,000

  

 

12

Revenue

 

		Three Months ended June 30,
		2024 $												2023 $
		Contracts with customers				Leasing				Total				Contracts with customers				Leasing				Total
Recurring - non-capital			1,180				280				1,460				1,302				300				1,602
Capital equipment			773				-				773				-				-				-
			1,953				280				2,233				1,302				300				1,602

 

 

		Six months ended June 30,
		2024 $												2023 $
		Contracts with customers				Leasing				Total				Contracts with customers				Leasing				Total
Recurring - non-capital			2,442				500				2,942				2,559				510				3,069
Capital equipment			1,201				-				1,201				393				-				393
			3,643				500				4,143				2,952				510				3,462

  

13

Nature of expenses

 

		Three months ended June 30, 2024 $				Three months ended June 30, 2023 $				Six months ended June 30, 2024 $				Six months ended June 30, 2023 $
Production and manufacturing costs			323				92				432				308
Salaries and benefits			4,380				3,107				8,372				6,864
Consulting fees			1,539				1,537				3,144				2,555
Research and development expense			978				574				1,734				1,390
Sales and marketing expenses			883				619				1,592				1,102
Amortization and depreciation			287				277				592				560
Share-based compensation			768				842				1,535				1,783
Rent			108				219				202				500
Software/Hardware			132				88				344				248
Insurance			325				359				656				719
Office and shop supplies			25				55				60				188
Other expenses			317				269				796				519
Expected credit loss (note 3)			1				-				(1	)			-
			10,066				8,038				19,458				16,736

 

 

14

Net finance expense/(income)

 

		Three months ended June 30, 2024 $				Three months ended June 30, 2023 $				Six months ended June 30, 2024 $				Six months ended June 30, 2023 $
Change in fair value of derivative financial instrument			-				353				-				232
Lease liability interest expense (note 9)			8				11				16				23
Other interest income on cash and cash equivalents			(476	)			(455	)			(1,038	)			(752	)
Interest income on trade and other receivables (note 3)			(99	)			(40	)			(168	)			(79	)
CIBC loan Interest expense (note 8)			154				181				323				361
Net foreign exchange (gain)/loss			(521	)			834				(1,389	)			954
			(934	)			884				(2,256	)			739

 

Credit risk

 

Credit risk is the risk of a financial loss to the Company if a counterparty to a financial instrument fails to meet its contractual obligation. The Company is exposed to credit risk on its cash and trade and other receivable balances. The Company’s cash management policies include ensuring cash is deposited in Canadian chartered banks.

 

The Company applies the IFRS 9 simplified approach to measuring expected credit losses, which uses a lifetime expected loss allowance for all trade receivables. To measure the expected credit losses, trade receivables are grouped based on shared credit risk characteristics and the days past due.

 

At June 30, 2024, the expected loss rates are based on comparable company payment profiles of sales over a period of 36 months before June 30, 2024 and the corresponding historical credit losses experienced within this period. The historical loss rates are adjusted to reflect current information on macroeconomic factors affecting the ability of the customers to settle the receivables.

 

The loss allowance as at June 30, 2024 for trade receivables is as follows:

 

																						2024
		Current				0–30 days				31-60 days				61-90 days				90+  days				Total
Expected loss rate			0.84	%			1.42	%			1.35	%			2.46	%			3.62	%
Gross carrying amount			6,214				132				42				-				573				6,961
Loss allowance			52				2				1				-				20				75

 

Foreign currency risk

 

Foreign currency risk occurs as a result of foreign exchange rate fluctuations between the time a transaction is recorded and the time it is settled.

 

 

The Company purchases goods and services denominated in foreign currencies and, accordingly, is subject to foreign currency risk. The Company’s financial instruments denominated in foreign currencies are shown below in US dollars.

 

														June 30, 2024
		US dollars $				Euro $				Canadian dollars $				Chinese renminbi $				Total $
Cash			32,141				880				897				161				34,079
Trade and other receivables			4,516				1,432				1,214				-				7,162
Accounts payable and accrued liabilities			(404	)			(409	)			(1,846	)			(12	)			(2,671	)
Lease liability			-				-				(685	)			-				(685	)
Long-term debt			-				-				(5,967	)			-				(5,967	)

 

As at June 30, 2024, if foreign exchange rates had been 5% higher, with all other variables held constant, loss and comprehensive loss would have been $217 higher, mainly as a result of the translation of foreign currency denominated cash, trade and other receivables, accounts payable and accrued liabilities, lease liability and long-term debt. The Company does not use derivatives to reduce exposure to foreign currency risk.

 

Liquidity risk

 

Liquidity risk is the risk the Company may encounter difficulties in meeting its financial liability obligations as they come due. The Company has a planning and budgeting process in place to help determine the funds required to support the Company’s normal operating requirements on an ongoing basis.

 

The Company controls liquidity risk through management of working capital, cash flows and the availability and sourcing of financing. The Company’s ability to accomplish all of its future strategic plans is dependent on obtaining additional financing or executing other strategic options by the second half of the year ending December 31, 2025; however, there is no assurance the Company will achieve these objectives.

 

The following table summarizes the Company’s significant contractual, undiscounted cash flows related to its financial liabilities.

 

														June 30, 2024
		Carrying amount $				Future cash flows $				Less than 1 year $				Between 1 year and 5 years $
Accounts payable and accrued liabilities			2,671				2,671				2,671				-
Lease liability			685				730				288				442
Long-term debt			5,967				7,166				2,480				4,686
			9,323				10,567				5,439				5,128

 

 

15

Loss per share

 

The following table shows the calculation of basic and diluted loss per share:

 

		Three months ended June 30, 2024				Three months ended June 30, 2023				Six months ended June 30, 2024				Six months ended June 30, 2023
Net loss for the period		$	6,919			$	7,355			$	13,118			$	14,096
Weighted average number of common shares			24,440,444				21,165,107				24,373,869				21,044,330
Basic and diluted loss per share		$	0.28			$	0.35			$	0.54			$	0.67

 

 

The computation of diluted loss per share is equal to the basic loss per share due to the anti-dilutive effect of the share options, RSUs and DSUs. Of the 1,481,408 share options (June 30, 2023 – 1,479,596), 458,895 RSUs (June 30, 2023 – 385,752), and 75,000 DSUs (June 30, 2023 – 50,000) not included in the calculation of diluted loss per share for the period ended June 30, 2024, 1,319,783 (June 30, 2023 – 1,158,702) were exercisable.

 

16

Related party transactions

 

Key management includes the Company’s directors and senior management team. The remuneration of directors and the senior management team was as follows:

 

		Three months ended June 30, 2024 $				Three months ended June 30, 2023 $				Six months ended June 30, 2024 $				Six months ended June 30, 2023 $
Salaries and employee benefits			673				253				1,023				731
Directors’ fees			69				75				138				156
Share-based compensation			485				577				1,027				1,354
			1,227				905				2,188				2,241

 

Executive employment agreements allow for additional payments in the event of a liquidity event, or if the executive is terminated without cause.

 

17

Segment reporting

 

The Company’s operations are categorized into one industry segment, which is medical technology focused on magnetic resonance guided ablation procedures for the treatments to ablate the prostate gland, uterine fibroids, osteoid osteoma and nerves for palliative pain relief for patients with metastatic bone disease. The Company is managed geographically in Canada, Germany, USA, China and Finland.

 

 

For the three months ended June 30, 2024:

 

		Canada $				USA $				Germany $				Total $
Revenue
Recurring - non-capital			99				1,101				260				1,460
Capital equipment			773				-				-				773
			872				1,101				260				2,233

 

For the six months ended June 30, 2024:

 

		Canada $				USA $				Germany $				Total $
Revenue
Recurring - non-capital			203				2,259				480				2,942
Capital equipment			773				-				428				1,201
			976				2,259				908				4,143

 

For the three months ended June 30, 2023:

 

		Canada $				USA $				Germany $				Total $
Revenue
Recurring - non-capital			99				1,286				217				1,602
			99				1,286				217				1,602

  

For the six months ended June 30, 2023:

 

		Canada $				USA $				Germany $				Total $
Revenue
Recurring - non-capital			140				2,346				583				3,069
Capital equipment			-				-				393				393
			140				2,346				976				3,462

 

Other financial information by segment as at and for the six months ended June 30, 2024:

 

		Canada $				USA $				Germany $				China $				Finland $				Total $
Total assets			40,817				3,823				1,907				175				3,310				50,032
Intangible assets			374				-				-				-				-				374
Property and equipment			131				549				-				-				-				680
Right-of-use assets			488				-				-				-				-				488
Amortization of intangible assets			101				-				-				-				-				101
Depreciation of property and equipment			28				355				-				-				-				383
Depreciation of right-of-use assets			108				-				-				-				-				108

 

 

Other financial information by segment as at and for the year ended December 31, 2023:

 

		Canada $				USA $				Germany $				China $				Finland $				Total $
Total assets			34,257				4,067				1,952				82				3,553				43,911
Intangible assets			490				-				-				-				-				490
Property and equipment			158				751				-				-				-				909
Right-of-use assets			616				-				-				-				-				616
Amortization of intangible assets			202				-				-				-				-				202
Depreciation of property and equipment			57				670				-				-				-				727
Depreciation of right-of-use assets			217				-				-				-				-				217

 

 

 

 

 

 

 

 

 

 

 

(13)

Exhibit 99.3

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

PROFOUND MEDICAL CORP.

 

 

 

 

 

MANAGEMENT’S DISCUSSION AND ANALYSIS

 

JUNE 30, 2024

 

PRESENTED IN US DOLLARS (000s)

 

 

 

 

 

 

The following Management’s Discussion and Analysis (“MD&A”) prepared as of August 8, 2024 should be read in conjunction with the March 31, 2024 unaudited interim condensed consolidated financial statements and related notes of Profound Medical Corp. (“Profound” or the “Company”). The unaudited interim condensed consolidated financial statements of Profound and related notes were prepared in accordance with International Financial Reporting Standards as issued by the International Accounting Standards Board (“IFRS Accounting Standards”) applicable to the preparation of interim financial statements, including International Accounting Standard 34, Interim Financial Reporting. Unless stated otherwise, all references to “$” are to United States dollars and all references to “C$” are to Canadian dollars. In this MD&A, unless the context requires otherwise, references to “Profound”, “the Company”, “we”, “us” or “our” are references to Profound Medical Corp. and its subsidiaries.

 

FORWARD-LOOKING STATEMENTS

 

This MD&A contains “forward-looking statements” within the meaning of Section 27A of the US Securities Act and Section 21E of the U.S. Securities Exchange Act of 1934, as amended (the “Exchange Act”) pursuant to the “safe harbor” provisions of the United States Private Securities Litigation Reform Act of 1995, and “forward-looking information” within the meaning of applicable Canadian securities laws, which include all statements other than statements of historical fact contained in this MD&A, such as statements that relate to the Company’s current expectations and views of future events. Often, but not always, forward-looking statements can be identified by the use of words such as “may”, “will”, “expect”, “anticipate”, “predict”, “aim”, “estimate”, “intend”, “plan”, “seek”, “believe”, “potential”, “continue”, “is/are likely to”, “is/are projected to” or the negative of these terms, or other similar expressions intended to identify forward-looking statements. These forward-looking statements include, among other things, statements relating to:

·

our expectations regarding the commercialization and adoption of our approved products (particularly the TULSA-PRO® system following US Food and Drug Administration (“FDA”) clearance) and our ability to generate revenues and achieve profitability;

·

our expectations regarding the safety, efficacy and advantages of our products over our competitors and alternative treatment options;

·

our expectations regarding our products fulfilling unmet clinical needs and achieving market acceptance among patients, physicians and clinicians;

·

our expectations regarding reimbursement for our approved products from third-party payors;

·

our expectations regarding an out-of-pocket market for the Company’s products;

·

our expectations regarding our relationships with Koninklijke Philips N.V. (“Philips”), Siemens Healthcare GmBH (“Siemens”) and GE Healthcare (“GE”), and our ability to achieve compatibility of our systems with magnetic resonance imaging (“MRI”) scanners produced by other manufacturers;

·

our ability to attract, develop and maintain relationships with other suppliers, manufacturers, distributors and strategic partners;

·

our expectations regarding our pipeline of product development, including expanding the clinical application of our products to cover additional indications;

·

our expectations regarding current and future clinical trials, including the timing, enrollment and results thereof;

·

our expectations regarding changes to existing regulatory frameworks;

·

our expectations regarding obtaining regulatory approvals;

·

our expectations regarding maintenance of the current regulatory approvals we have received, including our compliance with the conditions under such approvals, and the receipt of additional regulatory approvals for our products and future product candidates;

·

our mission and future growth plans;

·

our ability to attract and retain personnel;

·

our expectations regarding our competitive position for each of our products in the jurisdictions where they are approved;

·

our ability to manage our working capital and our ongoing ability to satisfy our cash requirements and any future commitments, financial obligations, covenants and contingencies;

·

our ability to raise debt and equity capital to fund future product development, pursue regulatory approvals and commercialize our approved products; and

·

anticipated trends and challenges in our business and the markets in which we operate.

 

Forward-looking statements involve known and unknown risks, uncertainties and other factors which may cause the actual results, performance or achievements of Profound to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements, including those factors discussed in the section entitled “Risk Factors” in the Company’s Annual Information Form prepared as of March 7, 2024 for the year ended December 31, 2023 (the “AIF”), available on SEDAR+ at www.sedarplus.ca and filed as an exhibit to the Company’s annual report on Form 40-F, filed on March 7, 2024 (the “40-F”), available on EDGAR at www.sec.gov, such as:

 

·

risks related to our limited operating history and history of net losses;

·

risks related to our liquidity and financing needs;

·

risks related to our ability to commercialize our approved products, including realizing the anticipated benefits of our co-development agreement with GE (the “GE Agreement”), expanding our sales and marketing capabilities, increasing our manufacturing and distribution capacity, increasing reimbursement coverage for our approved products and achieving and maintaining market acceptance for our products;

 

 

·

risks related to the regulation of our products, including in connection with obtaining regulatory approvals as well as post-marketing regulation;

·

risks related to our successful completion of clinical trials with respect to our products and future product candidates;

·

risks related to managing growth, including in respect of obtaining additional funding and establishing and maintaining collaborative partnerships, to achieve our goals;

·

risks related to competition that may impact market acceptance of our products and limit our growth;

·

risks relating to fluctuating input prices and currency exchange rates;

·

risks related to the reimbursement models in relevant jurisdictions that may not be advantageous;

·

risks related to reliance on third parties, including our collaborative partners, manufacturers, distributors and suppliers, and increasing the compatibility of our systems with MRI scanners;

·

risks related to intellectual property, including license rights that are key to our business;

·

risks related to product liability; and

·

risks related to the loss of key personnel.

 

Forward-looking statements contained herein are made as of the date of this MD&A and Profound disclaims any obligation to update any forward-looking statements, whether as a result of new information, future events or results or otherwise, unless required by applicable laws. There can be no assurance that forward-looking statements will prove to be accurate, as actual results and future events could differ materially from those anticipated in such statements. Accordingly, readers should not place undue reliance on forward-looking statements due to the inherent uncertainty in them. Readers are cautioned that while Profound believes it has accurately summarized all clinical studies cited in this MD&A, readers should review the full publications of the studies prior to making an investment decision in the Company.

 

BUSINESS OVERVIEW

 

Profound (NASDAQ: PROF; TSX: PRN) is a commercial-stage medical device company focused on the development and marketing of customizable, incision-free therapeutic systems for the image guided ablation of diseased tissue utilizing its platform technologies and leveraging the healthcare system’s existing imaging infrastructure. Profound’s lead product (the “TULSA-PRO^® system”) combines real-time MRI, robotically driven transurethral sweeping-action thermal ultrasound with closed-loop temperature feedback control for the ablation of prostate tissue. The product is comprised of one-time-use devices and durable equipment that are used in conjunction with a customer’s existing MRI scanner.

 

In August 2019, the TULSA-PRO^® system received FDA clearance as a Class II device in the United States of America (“United States” or “US”) for thermal ablation of prescribed prostate tissue, using transurethral ultrasound ablation (“TULSA^®”) based on the Company sponsored (“TACT”) whole gland ablation pivotal clinical study. It is also CE marked in the European Union (“EU”) for ablation of targeted prostate tissue (benign or malignant). The TULSA-PRO^® system was approved by Health Canada in November 2019.

 

Profound believes that, based on the Company’s TACT clinical data and additional studies conducted in the EU, physicians may elect to use TULSA-PRO^® to ablate benign or malignant prostate tissue in patients with a variety of prostate diseases. Prostate diseases include prostate cancer and benign prostatic hyperplasia (“BPH”). Prostate cancer is one of the most common types of cancer affecting men. The annual incidence of newly diagnosed cases in 2023 is estimated to reach 288,300 in the United States according to the American Cancer Society and in 2020 there were approximately 475,000 newly diagnosed cases of prostate cancer in Europe, according to the International Agency for Research on Cancer. The American Cancer Society further estimates that there are approximately 5.8 million men living with prostate cancer in these two geographic regions. Although ten-year survival outcomes for prostate cancer remain favorable, it is still one of most common causes of cancer deaths among men. BPH is a histologic diagnosis that refers to the proliferation of smooth muscle and epithelial cells within the prostatic transition zone. According to the American Urological Association, BPH is nearly ubiquitous in the aging male population with worldwide autopsy proven histological prevalence increases starting at ages 40 to 45 years, reaching 60% at age 60 and 80% at age 80.

 

Profound initiated the commercial launch of its lead product, the TULSA-PRO^® system in the United States in Q4 2019, treating the first patient in a non-trial setting in January 2020. On June 2, 2023, Profound Medical announced new CPT Category 1 Codes from the American Medical Association (“AMA”) for TULSA to treat prostate diseases, which will be effective January 1, 2025. In addition, Profound continues to support additional clinical trials in the United States and abroad to further increase the body of clinical evidence that may be needed particularly for reimbursement and coverage of its technologies by private and government healthcare providers. The Company continues to expand the compatibility of its TULSA-PRO^® system with additional MRI brands to broaden its ability to utilize the global MRI installed base and seek regulatory approvals of its products in additional international jurisdictions.

 

 

Profound’s second product, the Sonalleve^® system, is CE marked in the EU for the treatment of uterine fibroids and adenomyotic tissue, palliative pain relief associated with bone metastases, treatment of osteoid osteoma, and management of benign desmoid tumors and has also been approved by the regulatory bodies in China and South Korea for non-invasive treatment of uterine fibroids. In late 2020, Sonalleve^® received Humanitarian Device Exemption (“HDE”) approval from the FDA for the treatment of Osteoid Osteoma in the United States. The Sonalleve^® system is only compatible with certain Philips MRIs.

 

Profound deploys a recurring revenue business model in the United States to market TULSA-PRO^®, charging a one-time payment that includes a supply of its one-time-use devices, use of the system, as well as the Company’s customer and technological support (“Genius”) services that support each TULSA center. The Sonalleve^® product is marketed primarily outside North America in European and Asian countries, deploying a capital sales model. Outside of North America, Profound generates most of its revenues from its system sales in Europe and Asia, where the Company deploys a more traditional hybrid business model, charging for the system separately as a capital sale and an additional per patient charge for the one-time-use devices and associated Genius services.

 

Profound’s Technology

 

TULSA-PRO^® and Sonalleve^® share the common technological concept of using MRI to enable visualization by the surgeon of desired tissue in real time. Both products also use thermal ultrasound technology to gently heat and ablate tissue using the real-time thermometry capability of the MRI.

 

TULSA-PRO^® delivers its ultrasound energy through a transurethral catheter, a one-time-use device that is placed in the patient’s prostate through a natural orifice. Focused ultrasound energy is then delivered by the catheter in the shape of a blade. Externally the catheter is connected to a software controlled robotic manipulator that rotates up to 360-degree in a sweeping action to impart thermal energy and thus ablation of tissue. The real time temperature measurement of the prostate is coupled with closed loop process control that measures the appropriate amount of ultrasound energy to gently heat the physician-prescribed region of prostate tissue to the target temperature to achieve cell kill without boiling or charring the tissue. As a measure to keep the urethra within the prostate viable, the temperature of the transurethral catheter is maintained at an appropriate level by circulating water inside the catheter. Similarly, a water-cooled specially designed catheter is placed in the patient’s rectum during the ablation process to keep it protected from thermal damage during the procedure. The TULSA-PRO in conjunction with its Thermal Boost module, enables surgeons to temporarily increase the ablation target temperature in prostate regions where advanced stage cancer might reside, further increasing their confidence that aggressive cancer cells have been ablated. Profound believes that TULSA-PRO^®’s controlled and relatively gentle heating process may result in lower post procedural pain and complications, reduced potential of life affecting side effects, and in significantly desirable shrinkage of the prostate via resorption of the dead tissue over time, which may provide a longer-term durable benefit.

 

Sonalleve^® delivers its ultrasound energy via a disc located outside the patient. Its ultrasound energy is focused to create small cylindrical hot spots a certain distance into the patient. Overlapping cylinders create ablation of the physician-prescribed desired tissue. Similar to TULSA-PRO, Sonalleve^® also provides for controlled temperature increases to achieve cell kill.

 

The physician is in charge of using the Profound devices and decides which tissue needs to be ablated to impart therapeutic effect. Profound believes that in the hands of trained physicians, its systems have the ability to provide customizable, incision-free ablative therapies with the precision of real-time MRI visualization and thermometry, focused ultrasound and closed-loop temperature feedback control. Profound believes that its technology offers clinicians and appropriate patients a better alternative to traditional surgical or radiation therapies, with respect to clinical outcomes, side effects and recovery time.

 

TULSA-PRO^®

 

The TULSA-PRO^® system is designed to provide precise, flexible and durable ablation of a surgeon defined region of the prostate while actively protecting the urethra and rectum to help preserve the patient’s natural functional abilities. To date, over 3,000 global TULSA-PRO^® procedures have been performed by more than 100 physicians at over 30 commercial and 20 clinical research sites.

 

Clinical Studies

 

In March 2014, Profound completed enrollment and treatment of 30 patients in the Phase I TULSA multi-jurisdictional safety and precision study. Based on the Phase I clinical trial results, in April 2016, Profound received a CE Certificate of Conformity for the TULSA-PRO^® system from its notified body in the EU, and in the fourth quarter of 2016, Profound initiated a pilot commercial launch of TULSA-PRO^® in key European markets where the CE mark is accepted.

 

Profound received FDA clearance for the TULSA-PRO^® system in August 2019 for transurethral ultrasound ablation of prostate tissue, based on the Company’s TACT Pivotal Clinical Trial. The TACT Pivotal Clinical Trial is a prospective, open-label, single-arm pivotal clinical study, of 115 treatment-naïve localized prostate cancer patients across 13 research sites in the United States, Canada and Europe, which enrolled patients between August 2016 and February 2018.

 

 

Localized Prostate Cancer, Ablation Safety and Efficacy: TACT Pivotal Study

 

The TACT Pivotal Clinical Trial demonstrates that MRI-guided TULSA is a minimally invasive procedure for effective prostate cancer ablation with a favorable side effect profile, minimal impact on quality of life and low rates of residual disease¹. In the large, multi-center prospective study in men with predominately intermediate-risk prostate cancer, whole gland ablation sparing the urethra and apical sphincter with the TULSA-PRO^® met its primary regulatory endpoint of prostate-specific antigen (“PSA”) reduction in 96% of men to a median nadir of 0.34 ng/ml and 0.5 ng/ml at 12 months. Median decrease in perfused prostate volume as assessed by a central radiologist using 12-month MRI was 91%, from a median 37 cc to 2.8 cc. At 12 months, extensive biopsy sampling of the markedly reduced prostate volume demonstrated a benefit for nearly 80% of men. There was no evidence of cancer in 65% of men and 14% had low-volume clinically-insignificant disease. The authors, however, noted that thermally-fixed non-viable cells can retain their apparently-malignant tissue morphology, confounding Gleason grading and potentially introducing false positives². By two and five years, 7% and 21%, respectively, of men sought additional treatment for their prostate cancer (prostatectomy, radiation). The study patient population, with two-thirds of those with Gleason Grade Group (GGG) ≥ 2 having either bilateral disease or at least five positive cores, allowed for evaluation of oncologically relevant secondary outcomes including PSA stability, post-treatment biopsy, and salvage treatment. Notwithstanding the limitations of comparisons between ablative and extirpative therapies, the 21% 5-year rate of salvage treatment and 20% rate of residual clinically significant prostate cancer in intermediate-risk patients are in line with accepted rates of early failure or additional intervention after standard treatments and goals for retreatment after ablative therapies. By five years, the median PSA nadir further reduced to 0.26 ng/ml. PSA reduction was durable over the extended follow-up period, from 0.53 ng/ml at one year to 0.63 ng/ml at five years. 

 

TULSA was associated with a high degree of safety and maintenance of quality-of-life, durable to five years, comparing favorably to radical prostatectomy and other whole-gland ablation techniques. At 12 months, 96% of men returned to baseline urinary continence, and 75% of potent men maintained or returned to erections sufficient for penetration, with these rates remaining stable or further improving to five years. A total of 12 grade 3 adverse events occurred in 8% of men, including genitourinary infection (4%), urethral stricture (2%), urinary retention (1.7%), urethral calculus and pain (1%), and urinoma (1%), all resolved by 12 months. There were no grade 4 events, rectal injuries, severe incontinence requiring surgical intervention, or severe erectile dysfunction unresponsive to medication.

 

Localized Prostate Cancer, Durability of Outcomes: Phase I Safety and Precision Study

 

The Phase I Clinical Trial demonstrates that MRI-guided TULSA is safe and precise for ablation in patients with localized prostate cancer, providing spatial ablation precision of ± 1.3 mm with a well-tolerated side-effect profile and minor or no impact on urinary, erectile and bowel function at 12 months³. There were no grade 4 or higher adverse events, one transient attributable grade 3 event (epididymitis), and notably no injury to rectal or periprostatic structures. Functional outcomes, International Prostate Symptom Score (“IPSS”) and IIEF-15, both showed a favorable anticipated trend of initial deterioration with subsequent gradual improvement toward baseline levels. Consistent with the conservative whole-gland treatment plan which included a 3 mm circumferential margin expected to spare 10% viable prostate at the gland periphery, intra-operative MRI thermometry measured 90% thermal ablation of the prostate gland, median PSA decreased 90% from 5.8 ng/ml to nadir of 0.6 ng/ml, and median prostate volume reduced by 88% on 1-year MRI. Prostate biopsy at one year identified decreased cancer burden with 61% reduction in cancer length; however, attributable to the circumferential safety margin, clinically significant cancer in 9 of 29 men (31%), and any cancer in 16 of 29 (55%).

 

Follow-up data to three and five years demonstrate durability of the outcomes, with continued treatment safety and stable quality of life, as well as predictable PSA and biopsy oncological outcomes based on treatment-day imaging and early PSA follow-up, without precluding any potential salvage therapy options⁴. Repeat prostate biopsy at three years demonstrated durable histological outcomes, with only one subject upgrading to GGG 1 from negative at 12 months, and one subject upgrading to GGG 2 from GGG 1 at 12 months. Between one and five years, there were no new serious adverse events. By five years, 16 men completed protocol follow-up, three withdrew with PSA <0.4 ng/ml, 10 had salvage therapy without complications (six prostatectomy, three radiation and one laser ablation), and one died of an unrelated cause. Of 16 men with complete follow-up data, five-year median PSA remained at 0.55 ng/ml. Median IPSS of 6 at baseline returned to 5 by three months, and 6.5 at five years. At baseline, 9 of 16 had erections sufficient for penetration, 11 of 16 at one year, and 7 of 16 at five years. All 16 subjects had leak-free, pad-free continence at one and five years. Predictors of salvage therapy included lower ablation coverage and higher PSA nadir. At five years after TULSA, cancer specific survival is 100%, and overall survival 97%.

 

_______________________________

¹ Klotz et al, “MRI-guided transurethral ultrasound ablation of prostate cancer,” The Journal of Urology, 2020

² Anttinen et al, “Histopathological evaluation of prostate specimens after thermal ablation may be confounded by the presence of thermally-fixed cells,” International Journal of Hyperthermia, 2019

³ Chin et al, “Magnetic Resonance Imaging-Guided Transurethral Ultrasound Ablation of Prostate Tissue in Patients with Localized Prostate Cancer: A Prospective Phase 1 Clinical Trial,” European Urology, 2016; Bonekamp et al, “Twelve-month prostate volume reduction after MRI-guided transurethral ultrasound ablation of the prostate,” European Radiology, 2018

⁴ Nair et al, “MRI-Guided Transurethral Ultrasound Ablation in Patients with Localized Prostate Cancer: Three Year Outcomes of a Prospective Phase I Study”, BJU International, 2020; Nair et al, “PD17-03 Five-Year Outcomes from a Prospective Phase I Study of MRI-Guided Transurethral Ultrasound Ablation in Men with Localized Prostate Cancer”, AUA 2020 Virtual Experience, Abstract in The Journal of Urology, 2020; Hatiboglu et al, “Durability of functional outcomes after MRI-guided transurethral ultrasound ablation of the prostate,” JU Open Plus, 2023.

 

 

Benign Prostatic Hyperplasia (BPH), Relief of Lower Urinary Tract Symptoms (LUTS): Phase I Studies

 

Promising safety and feasibility of the TULSA-PRO^® to relieve Lower Urinary Tract Symptoms (“LUTS”) associated with BPH has been demonstrated in two clinical studies showing improvements in IPSS comparable to modern minimally invasive surgical therapies⁵. A retrospective analysis of a sub-group of nine men from the Phase I localized prostate cancer study who also had LUTS (baseline IPSS ≥ 12) demonstrated significant IPSS improvement of 58% from 16.1 to 6.3 at 12 months (p=0.003), with at least a moderate (≥ 6 points) symptom reduction in eight of nine patients. IPSS Quality of Life (“QoL”) improved in eight of nine patients. Erectile function (IIEF-EF) remained stable from 14.6 at baseline to 15.7 at 12 months. The proportion of patients with erections sufficient for penetration was unchanged. Full urinary continence (pad-free, leak-free) was achieved at 12 months in all patients. In five men who suffered from more severe symptoms (baseline IPSS ≥ 12 and Qmax < 15 ml/s), peak urine flow rate (“Qmax”) increased from 11.6 ml/s to 22.5 ml/s at 12 months. All adverse events were mild to moderate with no serious events reported.

 

A prospective Phase I/II study of TULSA-PRO^® for BPH has been conducted with early outcomes published in 2022⁶. All measures of urinary function and quality of life improved during the initial twelve-month follow up among the first ten patients treated, while no adverse effects were seen on sexual and bowel functions: average IPSS decreased from 17.5 to 4.0, IPSS QoL decreased from 4.0 to 0.5, and Qmax increased from 12.4 ml/s to 21.8 ml/s, among several other improved urinary measures. A single serious adverse event had occurred, abscess of the epididymis requiring drainage at two weeks post therapy. Enrollment of this study has been increased to 30 patients.

 

Radio-recurrent localized prostate cancer, Salvage TULSA (sTULSA): Phase I Study

 

Salvage ablation of radio-recurrent localized prostate cancer has been evaluated in a prospective Phase I/II study of TULSA-PRO^® with early outcomes published in 2020⁷. The report includes the first eleven patients from a 40-patient study, who were successfully treated, and discharged on the first postoperative day, with median catheterization time of seven days. Median PSA decreased from 7.6 ng/ml at baseline to a nadir of 0.2 ng/ml and was 0.23 ng/ml at 12 months. At 12 months, 10/11 patients were free of any PCa in the targeted ablation zone, confirmed with biopsy and imaging (MRI and PSMA-PET), and had low and stable PSA. Four patients had prolonged catheterization and subsequent urinary tract infection, and one of these patients had upper urinary tract dilation treated with double-J-stents.

 

Palliation of symptomatic locally advanced prostate cancer, Palliative TULSA (pTULSA): Phase I Study

 

Patients with symptomatic locally advanced prostate cancer can suffer from severe urinary retention due to bladder outlet obstruction, intractable hematuria and frequent hospitalization. While these complications are commonly treated by palliative transurethral resection of the prostate (“TURP”), the improvement is often insufficient and may exclude patients who cannot discontinue anticoagulants. The safety and feasibility of MRI-guided TULSA was evaluated as an alternative palliative treatment option for men suffering from symptomatic locally advanced prostate cancer⁸. Ten patients with locally advanced prostate cancer were enrolled, half with clinical stage T4 disease and half with clinical T3. Prior to TULSA, all patients had continuous indwelling catheterization due to urinary retention, and 90% had history of recurrent and/or ongoing gross hematuria. Three patients had palliative TURP performed six months prior to receiving palliative TULSA, all of which were unsuccessful. One week after palliative TULSA, 50% of men were catheter-free. At last follow-up, 100% of men were free of gross hematuria, and 80% had an improvement in catheterization, with 70% completely catheter-free. Notably, the average hospitalization time from local complications reduced from 7.3 to 1.4 days in the six-month period before and after palliative TULSA. All adverse events were related to urinary tract infections, with two patients requiring intravenous administration of antibiotics and three patients resolved with oral antibiotics alone. No other treatment related adverse events were recorded, with no rectal injury or fistula. Further, there was no need for blood transfusions and there was no perioperative mortality.

 

 

 

_______________________________

⁵ Elterman et al, “Relief of Lower Urinary Tract Symptoms after MRI-Guided Transurethral Ultrasound Ablation (TULSA) for localized prostate cancer: Subgroup Analyses in Patients with concurrent cancer and Benign Prostatic Hyperplasia,” Journal of Endourology, 2020; Anttinen et al, “Transurethral ultrasound therapy for benign prostatic obstruction in humans,” EAU 2020 Conference Presentation

⁶ Viitala et al, “Magnetic resonance imaging-guided transurethral ultrasound ablation for benign prostatic hyperplasia: 12-month clinical outcomes of a phase I study,” BJU Int, 2022.

⁷ Anttinen et al, “Salvage Magnetic Resonance Imaging–guided Transurethral Ultrasound Ablation for Localized Radiorecurrent Prostate Cancer: 12-Month Functional and Oncological Results,” European Urology Open Science, 2020.

⁸ Anttinen et al, “Palliative MRI-guided transurethral ultrasound ablation for symptomatic locally advanced prostate cancer,” Scandinavian Journal of Urology, 2020

 

 

CAPTAIN Trial

 

CAPTAIN (A Comparison of TULSA Procedure vs. Radical Prostatectomy in Participants with Localized Prostate Cancer) is a prospective, multi-centre randomized controlled trial of 201 patients aimed at comparing the safety and efficacy of the TULSA procedure (performed with the TULSA-PRO^® system) with radical prostatectomy (“RP”) in men with organ-confined, intermediate-risk, Gleason Score 7 (Grade Group 2 and 3) prostate cancer. In the CAPTAIN trial, 134 patients will be randomized to receive one or two TULSA procedures and 67 patients will be randomized to receive RP. The trial takes place primarily in the United States, with an additional two sites in Canada and one in Europe. Of those, seventeen sites have been activated to date and are currently recruiting patients.

 

RP is currently the gold-standard surgical treatment for intermediate-risk prostate cancer. RP effectively controls disease but carries risk of significant side effects such as long-term erectile dysfunction and urinary incontinence. The TULSA procedure combines transurethral, robotically-driven therapeutic ultrasound with real-time visualization of temperature and automated control of heating from magnetic resonance thermometry. The high spatial, thermal, and anatomic resolution of the target volume enables precise ablation of prostate tissue while sparing functionally important structures, potentially reducing the risk of side effects relative to RP.

 

The goal of the CAPTAIN trial is to demonstrate that the efficacy of the TULSA procedure is not inferior to RP, while demonstrating superior quality of life outcomes in patients receiving the TULSA procedure as compared to those patients receiving RP. The primary safety endpoint is the proportion of patients who preserve both erectile potency and urinary continence at one year after treatment. The primary efficacy endpoint is the proportion of patients who are free from any additional treatment for prostate cancer by three years after treatment. Secondary endpoints include comparison of rates of complications, cost effectiveness, and timing of the return to baseline activity. Long-term follow-up will be gathered for up to 10 years after treatment.

 

Sonalleve^®

 

Profound’s Sonalleve^® system combines real-time MRI and thermometry with focused ultrasound delivered from the outside of the patient to enable customized incision-free ablation of diseased tissue. Profound acquired the Sonalleve^® technology from Philips in 2017.

 

The Sonalleve^® system is CE marked in the EU for the treatment of uterine fibroids, adenomyotic tissue, palliative pain treatment of bone metastases, osteoid osteoma and management of benign tumors. The uterine fibroids application is also available for sale in Canada. In 2018, the Sonalleve^® system was also approved in China by the National Medical Products Administration for the non-invasive treatment of uterine fibroids and by the Ministry of Food and Drug Safety in South Korea. Philips Oy registered Sonalleve^® in several Middle East, North African, and South Asian countries. In 2020, Sonalleve® also received HDE from the US FDA for treatment of Osteoid Osteoma.

 

Sonalleve^® Clinical Applications

 

Uterine Fibroids and Adenomyosis

 

Uterine fibroids are the most common non-cancerous tumors in women of childbearing age. Both surgical and medical treatments are available, and the choice depends on number, size, and location of uterine fibroids, patient’s age and preferences, and pregnancy expectations. To date, symptomatic uterine fibroids have been mostly treated with radical surgery (hysterectomy) in women who have completed childbearing, or conservative surgery (myomectomy and endometrial ablation) in women who wish to preserve fertility. Today, the radiologist also has interventional options available. Minimally or non-invasive interventional radiology procedures include uterine artery embolization.

 

There is currently no ideal treatment for adenomyosis, and new options are needed. Drawing on experience of treatment of uterine fibroids, MR-High Intensity Focused Ultrasound (“MR-HIFU”) has been explored as a potential new conservative treatment and MR-HIFU is an early-stage, non-invasive, therapeutic technology with the potential to improve the QoL and decrease the cost of care for patients with adenomyosis.

 

To achieve its current regulatory clearances, the Sonalleve^® MR-HIFU System has undergone several studies and clinical trials for uterine applications at Sunnybrook Health Sciences Center (Toronto, Ontario), University Medical Center Utrecht (Utrecht, the Netherlands), National Institutes of Health (Bethesda, MD, USA), St. Luke’s Episcopal Hospital (Houston, TX, USA), University Hospital St. André (Bordeaux, France), Samsung Medical Center (Seoul, Korea), Peking University First Hospital Beijing (Beijing, China), First Affiliated Hospital of Medical College of Xi’an Jiaotong University (Xi’an, China), and Turku University Hospital (Turku, Finland), amongst others.

 

In addition, a comprehensive literature review provides supportive evidence showcasing the beneficial action of MR-HIFU in uterine fibroid and adenomyosis therapy. These studies include the Verpalen et al. 2020, Nguyen 2020, Yeo et al. 2017, Kim et al. 2017, and Hocquelet et al. 2017 that utilized the Sonalleve^® MR-HIFU System. Specifically, the studies show impressive performance in terms of ablation efficiency, therapeutic efficacy, symptom reduction, and/or QoL improvement. There were no treatment-related serious adverse events in any of these studies, although Browne et al. 2020 describes a procedure-related major complication in the form of deep vein thrombosis that was noted in one patient (0.8%) and subsequently and successfully treated with anticoagulation therapy. Minor adverse events, when present, typically include 1st and 2nd degree skin burns, local swelling, cramps, leg pain, abdominal pain, buttock pain, and back pain, which are all known and anticipated adverse events of MR-HIFU therapy.

 

 

Palliative Bone Pain Treatment

 

Pain caused by bone metastases is common in the event of malignancy and is inevitably associated with serious complications that may deteriorate the QoL of patients and become life threatening.

 

For patients with bone metastases, clinical evaluation reports were completed in October 2020, showing significant decrease in pain score and/or dosage of medication and increase in QoL are to be expected with MR-HIFU bone therapy. The randomized controlled Phase III study by Hurwitz et al. represents some of the most important clinical data that has been reported. In 112 subjects receiving MR-HIFU compared against 35 subjects receiving sham treatment, significant pain reduction at three months (decrease in worst NRS pain ≥ 2 without increase in pain medication) was 64.3% vs. 20.0% (p<0.001), with mean Numeric Pain Scale (“NRS”) reduction of 3.6 ± 3.1 vs. 0.7 ± 2.4 from an initial median NRS score of 7.0 in both groups. Improvement in average Brief Pain Inventory-Quality of Life at three months was 2.4 points superior in the MR-HIFU group (p<0.001), representing a clinically important reduction in impairment caused by bone metastasis pain.

 

The clinical data above shows that patients with bone metastases can expect a statistically significant decrease in pain scores and/or in medication dosage and increase in quality of life with MR-HIFU bone metastasis therapy.

 

Osteoid Osteoma Treatment

 

Osteoid osteoma is a relatively rare, painful bone tumor that typically occurs in the cortex of long bones, especially in children and adolescents, and accounts for approximately 10% of all benign bone tumors.

 

Current osteoid osteoma treatment options include surgery and radiofrequency ablation (“RFA”), which is a less invasive option than surgical resection. Although RFA can have a high success rate, the treatment is invasive and can potentially cause minor and major complications. It also exposes patients and operators to ionizing radiation associated with the CT imaging guidance.

 

Sonalleve^® MR-HIFU provides an optimal therapy choice for osteoid osteoma which is a precise, completely non-invasive, and free from ionizing radiation treatment. The recent studies have assessed the use of Sonalleve^® MR-HIFU in treatment of osteoid osteoma, showing a high clinical success rate and complete symptom resolution without any serious adverse effects and only few minor adverse effects that promptly resolve. The Sonalleve^® MR-HIFU device offers a novel, minimally invasive, MRI-guided method to treat osteoid osteoma safely and effectively. A desmoid tumor, also called desmoid fibromatosis or aggressive fibromatosis, is a non-metastasizing but locally aggressive proliferation of myofibroblasts that affects children and adults, with a peak incidence in early adulthood. Traditional management of desmoid tumors includes observation, surgical resection, radiation, and/or chemotherapy. Observation allows assessment of the rate of tumor growth and may be acceptable in small, slow-growing, or asymptomatic lesions. Surgical resection is often a highly morbid procedure and has a high rate of recurrence even with negative margins. Radiotherapy provides somewhat improved local control rates but the morbidity from radiation, including burns, fibrosis, chronic edema, and pathologic fractures, is problematic. In addition, the small but finite risk of a radiation-induced malignancy is particularly troublesome in this young patient population, considering the tumor being treated is benign.

 

Recently, MR-HIFU has been assessed as a non-invasive therapy of desmoid tumors, showing good clinical success and even complete tumor eradication in some cases with low number and relative mild adverse events, which typically promptly resolve. The Sonalleve^® MR-HIFU device offers a novel, non-invasive, MRI-guided method to treat desmoid tumors.

 

This technology is ideally suited for the treatment of desmoid tumors in a patient population that is generally young, otherwise healthy, and would like to avoid the morbidity of traditional surgical, radiation, and medical therapies for a benign disease. Magnetic resonance imaging provides visualization of critical neurovascular structures and allows sparing of these structures during therapy. While complete ablation of a desmoid tumor may not be possible in all cases because of involvement of these structures, significant reduction in tumor volume is often obtained with a corresponding improvement in pain and functional impairment. As the natural history of the disease often involves recurrence, the ability to re-treat with MR-HIFU without an upper dose limit is also an advantage. The clinical evidence to date demonstrates that MR-HIFU provides a safe and effective treatment of desmoid tumors.

 

 

 

 

Business Update and Sales Strategy

 

Profound initiated its launch of the TULSA-PRO^® system in the United States in Q4 2019 and the first patient was treated in the United States in a non-clinical trial setting in January 2020. Since then, Profound’s business model has evolved to a recurring revenue model that includes durable hardware usage, one-time-use devices and Profound’s Genius services, which includes necessary support for a productive start-up of the practice.

 

Profound has generated revenues from capital sales, one-time-use devices and related services, in the EU (principally in Germany) and Asia. For the six months ended June 30, 2024, approximately 55%, 22% and 23% of revenues were generated in the United States, EU and Asia, respectively, compared to approximately 68%, 28% and 4% of revenues which were generated in the United States, EU and Asia, respectively for the six months ended June 30, 2023. Revenue on a quarter over quarter basis is expected to fluctuate given the Company is maintaining a limited European commercial effort and remains primarily focused on the US market.

 

Profound’s TULSA-PRO^® system is primarily marketed to early adopter physicians who specialize in treatment of prostate disease including urologists and radiologists at opinion leading hospitals. TULSA-PRO^® services are available at either independent imaging centers or at hospital-based imaging centers.

 

Historically, treatment of conditions such as localized prostate disease and uterine fibroids have included surgical intervention. Over time, surgery has evolved from an ‘open’ technique, to laparoscopic, to robotic surgery. The motivation of surgeons behind this evolution has been to perform procedures that reduce invasiveness, improve clinical outcomes and reduce recovery times. Profound is seeking to take this concept to the next level by enabling customizable, incision-free therapies for the MRI-guided ablation of diseased tissue with the TULSA-PRO^® and Sonalleve^® systems. These incision-free and radiation-free procedures offer surgeons the option of providing predictable and customizable procedures that eliminate invasiveness, offer the potential to improve clinical outcomes and further reduce hospital stays and patient recovery times.

 

Profound is establishing its own direct sales and marketing teams for sales of TULSA-PRO^® systems and the one-time-use devices related thereto, as well as for Sonalleve^® systems in the jurisdictions where it is approved. The primary focus of Profound’s direct sales team is to cultivate adoption of the TULSA-PRO^® technology, support clinical customers with the TULSA-PRO^® procedures and increase the utilization of the systems and one-time-use devices. Profound expects to generate recurring revenues from the use of the system, one-time-use devices, clinical support and service maintenance.

 

On January 21, 2019, the Company entered into an agreement with Siemens (the “Siemens Agreement”). Under the Siemens Agreement, there is a one-time fixed license fee and per annum payments calculated based on annual volume of Profound’s systems that are interfaced to a Siemens MRI scanner. The initial term of the Siemens Agreement is five years and will be automatically extended for successive one-year terms thereafter unless terminated earlier. The Company also obtained a non-exclusive license to Siemens Access I interface software and reasonable support for the term of the Siemens Agreement.

 

On December 21, 2020, Profound signed the GE Agreement to expand provider access to TULSA-PRO^®. Pursuant to the terms of the GE Agreement, Profound has been supplied with additional information to utilize the ExSI interface, which has allowed Profound to interface with GE MRI scanners and GE is helping support the development efforts of Profound to achieve compatibility with its GE MRI scanners which was achieved on March 1, 2022 when the Company signed the first site agreement for a Tulsa-PRO^® system interfaced with a GE scanner.

 

On February 8, 2024, Profound entered into a non-exclusive collaboration with Siemens Healthineers, aimed at laying the groundwork for Profound to begin marketing a complete therapeutics solution, combining its TULSA-PRO^® system with the MAGNETOM Free.Max magnetic resonance scanner from Siemens Healthineers, via Profound’s own sales force. Profound will continue to market TULSA-PRO^® as a stand-alone offering, providing its customers with the flexibility to use the technology with the MR hardware of their choice.

 

Competition

 

TULSA-PRO^®

 

The TULSA-PRO^® system is intended to ablate benign and malignant prostate tissue, however there are other treatment options for prostate disease. There are currently no marketed devices indicated for the treatment of prostate diseases or prostate cancer and Profound’s FDA indication and CE mark in the EU also do not include treatment of any particular disease or condition. However, there are a number of devices indicated for the destruction or removal of prostate tissue and devices indicated for use in performing surgical procedures that physicians and surgeons currently utilize when treating patients with prostate disease, including prostate cancer. Approaches that physicians and surgeons currently use to address prostate disease include: (1) watchful waiting/active surveillance; (2) simple prostatectomy; (3) radical prostatectomy (includes open, laparoscopic and robotic procedures); (4) radiation therapies including, external beam radiation therapy, brachytherapy and high dose radiation; (5) cryoablation; and (6) trans-rectal high intensity focused ultrasound (“HIFU”). In addition, certain adjunct or less common procedures are used or are under development to address prostate disease, such as androgen deprivation therapy and proton beam therapy.

 

 

Each of the foregoing competing options have their own limitations and benefits and may only be appropriate for limited patient populations. For example, active surveillance is generally recommended for patients who have been diagnosed with earlier stage, lower risk, disease where the possibility of side effects from intervention may outweigh the expected benefit of the chosen procedure. For clinicians and patients, the gap between active surveillance and the most commonly utilized options of radical prostatectomy or radiation therapy, imposes the possibility of substantial side effects, creating a need for a less invasive methodology to remove diseased prostate tissue that is both radiation and incision-free, provides a more favorable side-effect profile, and allows for safe and effective salvage treatment options if required in the future.

 

Profound believes that the flexibility of the TULSA-PRO® system may allow the Company to demonstrate its use as a tool for ablating benign and malignant diseased prostate tissue with greater speed and precision than current options while minimizing potential side effects. Profound believes that the TULSA-PRO® system may overcome certain limitations of other devices and methodologies for removing or addressing diseased prostate tissue including HIFU, such as complications associated with trans-rectal delivery and limitations relating to prostate size and total ablation volume. Profound believes that a transurethral (inside out) ablation approach with millimeter accuracy has advantages over HIFU in ablating the whole gland safely, as well as ablating larger prescribed treatment plans for patients with multi-focal disease, BPH, and those who have prostate cancer concurrent with BPH.

 

Sonalleve^®

 

The treatment choices for uterine fibroids usually depend on the symptoms of the patient, size of the fibroid, desire for future pregnancy and preference of the treating gynecologist. The most common treatment options for uterine fibroids include: (1) hormonal medications including gonadotrophin releasing hormone agonists; (2) progesterone releasing intra-uterine devices; (3) surgical procedures such as hysterectomy and myomectomy; and (4) uterine artery embolization. Profound believes that the Sonalleve^® system may provide a treatment option that is more convenient and comfortable with fewer side effects than hormonal medications or surgical procedures, such as hysterectomy or myomectomy.

 

Reimbursement

 

Profound’s ability to successfully commercialize the Company’s products depends in large part on the extent to which coverage and adequate reimbursement for such products and related treatments or procedures will be available from government health administration authorities, government and private health insurers, and other organizations or third-party payors. Pricing and reimbursement procedures and decisions vary from country to country. Many government health authorities and private payors condition payment on the cost-effectiveness of the product. Even if a device is FDA cleared or CE marked or has received other regulatory clearance or approval, there is no guarantee that third-party payors will reimburse providers or patients for the cost of the device and related procedures or that the amount of such reimbursement will be adequate to cover the cost of the device. The availability of coverage and adequate reimbursement to hospitals and clinicians using Profound’s products therefore is important to its ability to generate revenue and Profound plans to pursue coverage and reimbursement for the Company’s products in the key markets where the Company has regulatory approvals. Successful commercialization of the Company’s approved products will also depend on the cost of the system and the availability of coverage and adequate reimbursement from third-party payors.

 

On July 11, 2024, it was announced that U.S. Centers for Medicare and Medicaid Services (“CMS”) has issued its proposed rules establishing, for the first time, a Category 1 CPT code for the TULSA procedure, effective January 1, 2025.

 

According to the proposed rule, TULSA will have 3 physician codes to cover how therapy is delivered depending on if there are one or two physicians involved in the procedure: 5x006 TULSA Device Management and 5x007 TULSA Treatment, when two physicians are involved in the procedure, and 5x008 TULSA Complete Procedure, when performed by a single physician. TULSA will have a 0-day global period, indicating that the payment associated with the codes will only cover the work performed on the day TULSA is performed. Physicians will thereby bill for any pre or post patient visit separately using existing codes. This will provide physicians with the most flexibility to assess the appropriate number of visits needed by each patient and enable their safe and fast recovery. TULSA codes have also been assigned to all three sites of service: Hospital Outpatient (“HOPD”), Ambulatory Surgical Center (“ASC”), and Private Office/Non-Facility (“OBL”). The spectrum of the location of service will ensure patients can be treated in whatever setting they and their physician believe appropriate and convenient for each patient.

 

For Hospital Payment, the proposed rule has established TULSA as a Level 6 Urology Ambulatory Payment Classification (“APC”) for 2025 for 5x008 of $9 (National Average). For ASCs, the facility payment for 5x008 will be $7 (National Average).

 

 

The Proposed Rule for the Physician Fee Schedule has set the total Facility (HOPD or ASC) Relative Value Units (“RVU”) at 6.53 for TULSA Device Management 5x006 and 14.68 RVU for the TULSA Treatment Physician 5x007 when 2 physicians are involved in the TULSA procedure. If one physician performs the complete TULSA procedure, the RVU is 18.01 for 5x008.

 

The Proposed Rule for Physician fee schedule for Non-Facility (OBL or Private Office) has set RVU at 16.50 for TULSA Device Management 5x006 and 267.47 RVU for the TULSA Treatment Physician 5x007 when 2 physicians are involved in the TULSA procedure. If one physician performs the complete TULSA procedure, the RVU is 276.65 for 5x008.

 

As noted above, the TULSA procedure will have a 0-day Global Period, which does not include payment for post-operative visits, while all other comparable prostate treatment procedures include payments for post-operative visits performed in the first 90 days. The typical range of post-operative office visits would be approximately 9-11 total RVUs in the first 90-days.

 

The below tables summarize the proposed rule Codes, RVUs and Facility Dollar Amounts.

 

Facility Fee Schedule:

 

CPT Code	Description	APC: HOPD	APC: ASC
5x008	TULSA Complete Procedure	$9,208.501	$7,195.001

¹ Amounts are exact, not in thousands.

 

Physician Fee Schedule:

 

CPT Code	Description	Physician Total RVU		Typical 90-Day Follow-up	Physician Total RVU with typical 90-day Follow-Up
		Facility (HOPD, ASC)	Non-Facility (OBL)		Facility	Non-Facility (OBL)
					(HOPD, ASC)
5x006	TULSA Device Management	6.53	16.50	9.39 - 11.67	15.92 - 18.20	25.89 - 28.17
5x007	TULSA Treatment	14.68	267.47	n/a	14.68	267.47
5x006 & 5x007 Total	Procedure Total	21.21	283.97	9.39 - 11.67	30.60 - 32.88	293.36 - 295.64
	(Two Physician)
5x008	TULSA Complete Procedure (One Physician)	18.01	276.65	9.39 - 11.67	27.40 - 29.68	286.04 - 288.32

 

HIGHLIGHTS

 

§

On May 6, 2024 Profound announced the growing body of papers, posters and podium presentations regarding the potential for Profound Medical’s TULSA procedure becoming a mainstream treatment modality.

§

On May 9, 2024 Profound issued full-year 2024 revenue guidance.

§

On May 14, 2024, Profound received U.S. FDA 510(k) clearance for ‘Contouring Assistant’ AI module.

§

On May 15, 2024, Profound held its 2023 Annual General Meeting of Shareholders, at which Profound’s shareholders elected all six nominees to its board of directors.

§

On July 11, 2024, Profound announced Category 1 CPT codes proposed CY2025 rule for TULSA to treat prostate diseases.

 

 

SELECTED FINANCIAL INFORMATION

 

The following selected financial information as at and for the six months ended June 30, 2024, 2023 and 2022, have been derived from the unaudited interim condensed consolidated financial statements and should be read in conjunction with those unaudited interim condensed consolidated financial statements and related notes.

 

		For six months ended June 30, 2024 2023 2022
			$				$				$
Revenue			4,143				3,462				3,389
Operating expenses			18,022				15,537				16,442
Net finance expense (income)			(2,256	)			739				(972	)
Net loss for the period			13,118				14,096				14,145
Basic and diluted loss per share			0.54				0.67				0.68

 

		June 30, 2024 $				December 31, 2023 $
Total assets			50,032				43,911
Total non-current financial liabilities			4,370				5,578

 

Revenue has increased for the six months ended June 30, 2024 due to higher capital sales compared to the six months ended June 30, 2023 and 2022.

 

Operating expenses increased for the six months ended June 30, 2024 compared to the six months ended June 30, 2023 and 2022 due to the continued focus of commercialization of the TULSA-PRO^® within the US market based on increased research and development as well as selling and distribution expenses attributed to personnel and marketing.

 

The increase in net finance income for the six months ended June 30, 2024 compared to the six months ended June 30, 2023 and 2022 was primarily the impact of the change in the foreign exchange rates for Profound’s foreign currency denominated cash and interest income from cash held in the bank.

 

The Company reported total assets of $50,032 as at June 30, 2024 compared to $43,911 as at December 31, 2023. The increase in 2024 was primarily the result of the Public Offering and Private Placement for net proceeds of $21,079.

 

The Company reported total non-current financial liabilities of $4,370 as at June 30, 2024 compared to $5,578 as at December 31, 2023. The decrease in the six month period of 2024 was a result of the monthly repayments of the CIBC Loan balance.

 

 

RESULTS OF OPERATIONS

 

		Three months ended June 30																Six months ended June 30
		2024				2023				Change								2024				2023				Change
		$				$				$				%				$				$				$				%
Revenue			2,233				1,602				631				39	%			4,143				3,462				681				20	%
Cost of sales			795				552				243				44	%			1,436				1,199				237				20	%
Gross profit			1,438				1,050				388				37	%			2,707				2,263				444				20	%
Expenses
Research and development			4,193				3,155				1,038				33	%			8,126				6,995				1,131				16	%
General and administrative			2,109				2,080				29				1	%			4,496				4,186				310				7	%
Selling and distribution			2,969				2,251				718				32	%			5,400				4,356				1,044				24	%
Total operating expenses			9,271				7,486				1,785				24	%			18,022				15,537				2,485				16	%
Net finance (income)/expense			(934	)			884				(1,818	)			-206	%			(2,256	)			739				(2,995	)			-405	%
Loss before income taxes			6,899				7,320				(421	)			-6	%			13,059				14,013				(954	)			-7	%
Income taxes			20				35				(15	)			-43	%			59				83				(24	)			-29	%
Net loss attributed to shareholders for the period			6,919				7,355				(436	)			-6	%			13,118				14,096				(978	)			-7	%
Other comprehensive loss/(income)
Item that may be reclassified to profit or loss
Foreign currency translation adjustment			(2,068	)			4,117				(6,185	)			-150	%			(7,277	)			4,164				(11,441	)			-275	%
Net loss and comprehensive loss for the period			4,851				11,472				(6,621	)			-58	%			5,841				18,260				(12,419	)			-68	%
Loss per share
Basic and diluted net loss per Common Share			0.28				0.35				(0.07	)			-20	%			0.54				0.67				(0.13	)			-19	%

 

 

Revenue

 

Profound deploys a recurring revenue business model in the US to market TULSA-PRO^®, charging a one-time payment that includes a supply of its one-time-use device, use of the system as well as Company’s Genius services that support each TULSA center with clinical and patient recruitment. The Sonalleve^® product is marketed primarily outside North America in European and Asian countries deploying a one-time capital sales model with limited recurring service revenue. Outside of North America, Profound generates most of its revenues from its system sales (both TULSA-PRO^® and Sonalleve^®) in Europe and Asia where the Company deploys a more traditional hybrid business model, charging for the system separately as capital and an additional per patient charge for the one-time-use devices and associated Genius services. Revenue is comprised of recurring – non-capital revenue, which consists of the sale of one-time-use devices, lease of medical devices, procedures and services associated with extended warranties and one-time sale of capital equipment.

 

For the three months ended June 30, 2024, the Company recorded revenue totaling $2,233 with $773 from the one-time sale of capital equipment and $1,460 coming from recurring – non-capital revenue. For the three months ended June 30, 2023, the Company recorded revenue totaling $1,602 with $1,602 all coming from recurring – non-capital revenue. The increase in revenue for the three months ended June 30, 2024, was a result of higher capital sales. Revenue on a quarter over quarter basis is expected to fluctuate in the near term given the Company is maintaining a limited European commercial effort and remains focused primarily on the US market which continues to see growth quarter over quarter.

 

For the six months ended June 30, 2024, the Company recorded revenue totaling $4,143 with $1,201 from the one-time sale of capital equipment and $2,942 from recurring – non-capital revenue, which consists of the sale of one-time-use devices, lease of medical devices, procedures and services associated with extended warranties. For the six months ended June 30, 2023, the Company recorded revenue totaling $3,462 with $393 from the one-time sale of capital equipment and $3,069 from recurring – non-capital revenue, which consists of the sale of one-time-use devices, lease of medical devices, procedures and services associated with extended warranties. The increase in revenue for the six months ended June 30, 2024, was the result of higher capital sales.

 

Cost of sales

 

Cost of sales includes cost of finished goods, inventory provisions, warranty, freight and manufacturing overhead expenses.

 

For the three months ended June 30, 2024, the Company recorded cost of sales of $795, related to the sale of medical devices, capital and non-capital, which reflects a 64% gross profit margin. For the three months ended June 30, 2023, the Company recorded cost of sales of $552, related to the sale of medical devices, capital and non-capital, which reflects a 66% gross profit margin. The gross profit margin was slightly lower in 2024 due to the revenue product mix.

 

For the six months ended June 30, 2024, the Company recorded cost of sales of $1,436, related to the sale of medical devices, capital and non-capital, which reflects a 65% gross profit margin. For the six months ended June 30, 2023, the Company recorded a cost of sales of $1,199, related to the sale of medical devices, capital and non-capital, which reflects a 65% gross profit margin. The gross profit margin was consistent for the two periods.

 

Operating Expenses

 

Operating expenses consist of three components: research and development (“R&D”), general and administrative (“G&A”) and selling and distribution expenses. Historically, R&D expenses have exceeded selling and distribution expenses; however, in the future Profound expects selling and distribution expenses to increase as the Company further commercializes the TULSA-PRO^® system in the US.

 

R&D Expenses

 

R&D expenses are comprised of costs incurred in performing R&D activities, including new product development, continuous product improvement, investment in clinical trials and related clinical manufacturing costs, materials and supplies, salaries and benefits, consulting fees, patent procurement costs, and occupancy costs related to R&D activity.

 

For the three months ended June 30, 2024, R&D expenses were higher by $1,038 compared to the three months ended June 30, 2023. Material and salaries and benefits increased by $431 and $642, respectively. The increases were due to various R&D projects undertaken during the period which included fixture developments, yield improvements and additional materials for clinical trials, higher headcount and lower reimbursement of workforce costs. Offsetting these amounts was a decrease of $36 in share based compensation due to fewer awards granted to employees.

 

For the six months ended June 30, 2024, R&D expenses were higher by $1,131 compared to the six months ended June 30, 2023. Clinical trial costs, materials and salaries and benefits increased by $214, $482 and $656, respectively. The increase in clinical trial costs was due to CAPTAIN trial treatments and recruitment efforts, materials expenses were higher due to spending on R&D initiatives for fixture development and yield improvements and salaries increased due to higher headcount and lower reimbursement of workforce costs. Offsetting these amounts was a decrease in rent of $113 due to lower MRI time usage and a decrease of $104 to share based compensation due to fewer awards granted to employees.

 

 

G&A expenses

 

G&A expenses are comprised of management costs, including salaries and benefits, various management and administrative support functions, insurance and other operating and occupancy costs.

 

G&A expenses for the three months ended June 30, 2024 increased by $29 compared to the three months ended June 30, 2023. Salaries and benefits increased by $158 due to higher cost of living salary increases. Offsetting this amount was a decrease to insurance expense of $34 due to lower premium rates and decrease to consulting fees of $91 due to lower legal and financing fees.

 

G&A expenses for the six months ended June 30, 2024 increased by $310 compared to the six months ended June 30, 2023. Salaries and benefits and consulting fees increased by $236 and $155, respectively, due to higher cost of living salary increases and increased legal and accounting fees. Offsetting these amounts was a decrease in insurance costs of $63 due to lower premium rates and decrease to the general office expenses of $22.

 

Selling and distribution expenses

 

Selling and distribution expenses are comprised of business development costs related to the market development activities and commercialization of the Company’s systems, including salaries and benefits, marketing support functions, occupancy costs related to marketing activity and other miscellaneous marketing costs.

 

Selling and distribution expenses for the three months ended June 30, 2024 were higher by $718 compared to the three months ended June 30, 2023. Salaries and benefits, consulting fees and travel increased by $493, $106 and $117, respectively, due to increased salesforce and commission payments, consultants engaged to assist with Veteran Affairs and military sales markets and increased in-person conferences and customer meetings.

 

Selling and distribution expenses for the six months ended June 30, 2024 were higher by $1,044 compared to the six months ended June 30, 2023. Salaries and benefits consulting fees, marketing expenses and travel increased by $669, $174, $145 and $206, respectively due to increased salesforce and commission payments, consultants engaged to assist with Veteran Affairs and military sales markets, release of commercial segments and marketing advertisement campaigns, and increased in-person conferences and customer meetings. Offsetting these amounts was a decrease in share based compensation of $117 due to fewer awards granted to employees and a decrease to the general office expenses of $39.

 

Net finance expense/(income)

 

Net finance expense/(income) is primarily comprised of the following: (i) the CIBC Loan Agreement (as defined herein) accreting to the principal amount repayable and its related interest expense; (ii) the change in the fair value of the derivative liability warrants; (iii) the lease liability interest expense; (iv) foreign exchange gain or losses; (v) interest income from cash and cash equivalents; and (vi) the interest income on trade and other receivables.

 

Net finance income for the three months ended June 30, 2024, was higher by $1,818 compared to the three months ended June 30, 2023. During the three months ended June 30, 2024, the Company recognized $521 of foreign exchange gain and $99 interest income on trade and other receivables. The Company also recognized interest income from cash and cash equivalents of $476, interest expense from the CIBC Loan Agreement of $154 and lease liability interest expense of $8. The largest fluctuation from the three months ended June 30, 2024 versus the three months ended June 30, 2023 was the $353 decrease in fair value of the derivative liability warrants and $1,355 increase in foreign exchange gain.

 

Net finance income for the six months ended June 30, 2024, was higher by $2,995 compared to the six months ended June 30, 2023. During the six months ended June 30, 2024, the Company recognized $1,389 of foreign exchange gain and $168 interest income on trade and other receivables. The Company also recognized interest income from cash and cash equivalents of $1,038, interest expense from the CIBC Loan Agreement of $323 and lease liability interest expense of $16. The largest fluctuation from the six months ended June 30, 2024 versus the six months ended June 30, 2023 was the $2,343 increase in foreign exchange gain, $232 change in fair value of the derivative liability warrants and a $286 increase in interest income attributed to the increase in cash balance and the prime rate.

 

 

 

Net loss

 

Net loss for the three months ended June 30, 2024, was $6,919 or $0.28 per Common Share, compared to a net loss of $7,355 or $0.35 per Common Share for the three months ended June 30, 2023. The decrease in net loss was primarily attributed to an increase in net finance income of $1,818 and an increase in gross profits of $388. This was offset by an increase in R&D expense of $1,038, an increase in G&A expenses of $29 and an increase in selling and distribution expenses of $718.

 

Net loss for the six months ended June 30, 2024, was $13,118 or $0.54 per Common Share, compared to a net loss of $14,096 or $0.67 per Common Share for the six months ended June 30, 2023. The decrease in net loss was primarily attributed to an increase in net finance income of $2,995 and an increase in gross profits of $444. This was offset by an increase in R&D expense of $1,131, an increase in G&A expenses of $310 and an increase in selling and distribution expenses of $1,044.

 

SUMMARY OF QUARTERLY FINANCIAL RESULTS

 

The summary financial information provided below is derived from the Company’s interim financial statements for each of the last eight quarters that are prepared under IFRS Accounting Standards in US dollars.

 

		2024								2023																2022
			Q2 $				Q1 $				Q4 $				Q3 $				Q2 $				Q1 $				Q4 $				Q3 $
Revenue			2,233				1,910				2,009				1,728				1,602				1,860				1,257				2,035
Cost of sales			795				641				950				668				552				647				698				945
Gross profit			1,438				1,269				1,059				1,060				1,050				1,213				559				1,090
Operating expenses			9,271				8,751				9,841				7,620				7,486				8,051				9,381				9,324
Net finance expense/ (income)			(934	)			(1,322	)			356				(1,014	)			884				(145	)			499				(3,271	)
Loss before income taxes			6,899				6,160				9,138				5,546				7,320				6,693				9,321				4,963
Income taxes			20				39				(229	)			18				35				48				206				34
Net loss for the period			6,919				6,199				8,909				5,564				7,355				6,741				9,527				4,997
Loss per common share
Basic and diluted			0.28				0.26				0.42				0.26				0.35				0.32				0.46				0.24

 

The second quarter of 2024 revenue increased compared to the prior quarter as a result of capital sales. Operating expenses were higher due to the increase in headcount and lower workforce reimbursement from the European ministry of research. In addition, there was an increase in finance income due to the US dollar and Euro foreign currency rate, triggering a foreign exchange gain.

 

The first quarter of 2024 revenue increased compared to the majority of prior quarters as a result of higher US sales from recurring revenue. Operating expenses increased against several of the prior quarters due to additional headcount within sales and distribution and expenses associated with the continued TULSA-PRO^® commercialization with the US market.

 

In the fourth quarter of 2023 revenue continued to increase compared to prior quarters as new sites became operational and increased patient procedures. Operating expenses were higher than prior quarters due to ATM offering fees as well as overall increase to the salesforce.

 

In the third quarter of 2023 operating expenses were higher compared to the prior quarter due to increased consulting costs associated with regulatory and foreign consultants for additional approval in other countries. In addition, there was also an increase in finance income due to the US dollar and Euro foreign currency rate, triggering a foreign exchange gain.

 

The second quarter of 2023 revenue was lower compared to the prior quarter due to decreased one-time capital sales. Operating expenses were lower compared to the prior quarters due to decreased share based compensation expenses and lower amortization expenses as a result of intangible assets being fully amortized.

 

 

The first quarter of 2023 cost of sales decreased from the quarterly periods in 2022 as a result of manufacturing operating at a higher efficiency rate based on improvements to quality and training that were implemented in the manufacturing process.

 

The fourth quarter of 2022 revenue was lower compared to prior quarters due to decreased one-time capital sales, primarily resulting from lower capital sales than previous quarters. Operating expenses were higher due to goodwill impairment.

 

The third quarter of 2022 cost of sales decreased as a result of better yields and product quality. In addition, there was also an increase in finance income due to the US dollar and Euro foreign currency rates, triggering a foreign exchange gain.

 

LIQUIDITY AND CAPITAL RESOURCES

 

At June 30, 2024, the Company had cash of $34,079 compared to $26,213 at December 31, 2023. Historically, the Company’s primary source of cash has been financing activities, e.g., equity offerings as well as the CIBC Loan (as defined below).

 

Use of Proceeds

 

2024 Offering and non-brokered private placement

 

The Company received net proceeds of $21,079 from the Public Offering and Private Placement. The Company intends to use net proceeds from the Public Offering and Private Placement to fund the continued commercialization of the TULSA-PRO^® system in the United States, the continued development and commercialization of the TULSA-PRO^® system and the SONALLEVE^® system globally and for working capital and general corporate purposes. The Company confirms that there have been no material variances in the estimated use of proceeds from the net proceeds of the Public Offering since the date of the Company’s prospectus supplement dated December 27, 2023. In addition, there have been no material adjustments to the cost or timing of the business objective previously disclosed in such prospectus supplement.

 

		Total spending as at June 30, 2024
		$
TULSA-PRO® commercialization			9,418
Sonalleve® development and commercialization			1,576
Working capital and general corporate purposes			6,033
Total			17,027

 

 

CIBC Loan

 

Profound Medical Inc. (“PMI”) entered into a loan agreement with Canadian Imperial Bank of Commerce (“CIBC”) on November 3, 2022 (the “CIBC Loan Agreement”), for gross proceeds of C$10,000, maturing on November 3, 2027, with an interest rate based on CIBC prime plus 2% (the “CIBC Loan”). The Company was required to make interest-only payments until October 31, 2023, and monthly repayments on the principal of C$208 plus accrued interest commenced on October 31, 2023. All obligations of the Company under the CIBC Loan Agreement are guaranteed by current and future subsidiaries of the Company and included security of first priority interests in the assets of the Company and its subsidiaries. Initially, the Company had financial covenants in relation to the CIBC loan where unrestricted cash is at all times greater than EBITDA for the most recent six-month period, reported on a monthly basis and that revenue for any fiscal quarter must be 15% greater than revenue for the same fiscal quarter in the prior fiscal year, reported on a quarterly basis.

 

On September 26, 2023 an amendment to the CIBC Loan resulted in a change to the financial covenants. The amended covenants are that unrestricted cash must at all times be greater of: (i) to the extent EBITDA is negative for such period, EBITDA for the most recent nine-month period or (ii) $7,500, reported on a monthly basis; and that recurring revenue for any fiscal quarter must be 15% greater than recurring revenue for the same fiscal quarter in the prior fiscal year, reported on a quarterly basis. On March 31, 2024, the Company was in breach of the second covenant whereby revenue for any fiscal quarter must be 15% greater than revenue for the same fiscal quarter in the prior fiscal year. The Company received a waiver from CIBC in relation to this covenant breach.

 

On May 3, 2024, a second amendment to the CIBC Loan resulted in another amendment to the financial covenants. The amended covenants are that the recurring revenue covenant shall not be tested for any fiscal quarter in the 2024 fiscal year so long as unrestricted cash is no less than 2.5 multiplied by the principal amount of outstanding CIBC Loan at all times. The Company is in compliance with these financial covenants as at June 30, 2024.

 

 

Cash Flow

 

The Company manages liquidity risk by monitoring actual and projected cash flows. A cash flow forecast is performed regularly to ensure that the Company has sufficient cash to meet operational needs while maintaining sufficient liquidity. The Company’s cash requirements depend on numerous factors, including market acceptance of the Company’s products, the resources devoted to developing and supporting the products and other factors. Profound expects to continue to devote substantial resources to expand procedure adoption and acceptance of the Company’s products.

 

The Company may require additional capital to fund R&D activities and any significant expansion of operations by the second half of the year ending December 31, 2025. Potential sources of capital could include equity and/or debt financings, development agreements or marketing agreements, the collection of revenue resulting from future commercialization activities and/or new strategic partnership agreements to fund some or all costs of development. There can be no assurance that the Company will be able to obtain the capital sufficient to meet any or all of the Company’s needs. The availability of equity or debt financing will be affected by, among other things, the results of R&D, the Company’s ability to obtain regulatory approvals, the market acceptance of the Company’s products, the state of the capital markets generally, strategic alliance agreements and other relevant commercial considerations. In addition, if the Company raises additional funds by issuing equity securities, existing security holders will likely experience dilution, and any incurring of indebtedness would result in increased debt service obligations and could require the Company to agree to operating and financial covenants that would restrict operations. Any failure on the Company’s part to raise additional funds on terms favourable to the Company or at all may require the Company to significantly change or curtail current or planned operations in order to conserve cash until such time, if ever, that sufficient proceeds from operations are generated, and could result in the Company not being in a position to take advantage of business opportunities, in the termination or delay of clinical trials for its products, in curtailment of product development programs designed to identify new products, in the sale or assignment of rights to technologies, product and/or an inability to file market approval applications at all or in time to competitively market products.

 

		Three months ended June 30,								Six months ended June 30,
		2024 $				2023 $				2024 $				2023$
Cash provided by (used in) operating activities			(6,350	)			(5,119	)			(11,448	)			(10,942	)
Cash provided by (used in) financing activities			(675	)			-				19,708				2,144
Foreign exchange on cash			(76	)			1,410				(394	)			1,556
Net increase (decrease) in cash			(7,101	)			(3,709	)			7,866				(7,242	)

 

Operating Activities

 

Net cash provided by (used in) operating activities for the three months ended June 30, 2024 was $(6,350) versus $(5,119) for the three months ended June 30, 2023. The principal use of the operating cash flows during this period related to increased headcount, consulting expenses and marketing efforts in the US.

 

Net cash provided by (used in) operating activities for the six months ended June 30, 2024 was $(11,448) versus $(10,942) for the six months ended June 30, 2023. The primary change of the operating cash flows during this period related to increased headcount and consulting expenses.

 

Financing Activities

 

Net cash provided by (used in) financing activities for the three months ended June 30, 2024 was $(675) versus $nil for the three months ended June 30, 2023. These cash flows relate to monthly payments of the long-term debt and lease liability.

 

Net cash provided by (used in) financing activities for the six months ended June 30, 2024 was $19,708 versus $2,144 for the six months ended June 30, 2023. These cash flows relate primarily to the 2024 Offering and non-brokered private placement pursuant to which the Company received net proceeds of $21,079.

 

Foreign Exchange on Cash

 

Cash was impacted by the change in the foreign exchange rates for the Company’s foreign currency denominated cash (non-USD). The value of the Company’s currencies decreased, resulting in a decrease in the Company’s cash holdings.

 

 

Contractual obligations

 

The following table summarizes the Company’s significant contractual obligations:

 

										June 30, 2024
			Carrying amount $				Future cash flows $				Less than 1 Year $				Between 1 year and 5 years $
Accounts payables and accrued liabilities			2,671				2,671				2,671				-
Lease liability			6851				730				288				442
Long-term debt			5,967				7,166				2,480				4,686
Total			9,323				10,567				5,439				5,128

¹ Present value of the lease payments that are not paid, discounted using the interest rate implicit in the lease.

 

Non-GAAP Financial Measures

 

Non-GAAP measures are not recognized measures under IFRS Accounting Standards and do not have a standardized meaning prescribed by IFRS Accounting Standards. These measures are defined with reference to the nearest comparable IFRS Accounting Standards measure such that a reconciliation to the nearest comparable IFRS Accounting Standards measure can be completed. Accordingly, these measures may not be comparable to similar measures presented by other companies. Profound uses non-GAAP measures in order to provide additional financial information to complement the closest IFRS Accounting Standards measures in order to provide investors with a further understanding of the Company’s operations from management’s perspective. Investors should not consider that these non-GAAP measures are a substitute for analyses of the financial information that Profound reports under IFRS Accounting Standards. Profound uses these non-GAAP measures in order to provide investors with a supplemental measure of its operating performance and thus highlight trends in the Company’s business that may not otherwise be apparent when relying solely on IFRS Accounting Standards measures.

 

The Company’s working capital (defined as current assets less current liabilities) is a non-GAAP financial measure. Working capital is used to fund operations and meet short-term obligations. If the Company has enough working capital, it can continue to pay its employees and suppliers and meet other obligations, such as interest payments and taxes, even if it runs into cash flow challenges. The working capital as at June 30, 2024 and December 31, 2023 is set forth in the table below.

 

		June 30, 2024 $				December 31, 2023 $
Current assets			48,490				41,896
Less: Current liabilities			5,629				6,366
Working capital			42,861				35,530

 

Working capital increased by $7,331 with a surplus of $42,861 at June 30, 2024 compared to the surplus of $35,530 at December 31, 2023. The change in working capital is due to an increase in current assets of $6,594, which was primarily the result of the increase in the cash balance of $7,866 which was offset by decreases in prepaids expenses and deposits of $889. Current liabilities decreased by $737 due to a decrease in accounts payable and accrued liabilities and current portion of the long-term debt.

 

COMMITMENTS & CONTINGENCIES

 

All directors and officers of the Company are indemnified by the Company for various items including, but not limited to, all costs to settle lawsuits or actions due to their association with the Company, subject to certain restrictions. The Company has purchased directors’ and officers’ liability insurance to mitigate the cost of any potential future lawsuits or actions. The term of the indemnification is not explicitly defined but is limited to events for the period during which the indemnified party served as a director or officer of the Company. The maximum amount of any potential future payment cannot be reasonably estimated but could have a material adverse effect on the Company.

 

 

The Company has also indemnified certain lenders and underwriters in relation to certain debt and equity offerings and their respective affiliates and directors, officers, employees, shareholders, partners, advisers and agents and each other person, if any, controlling any of the underwriters or lenders or their affiliates against certain liabilities.

 

FINANCIAL INSTRUMENTS

 

The Company’s financial instruments consist of cash, trade and other receivables, accounts payable and accrued liabilities, derivative financial instruments, lease liability and long-term debt. The fair values of these financial instruments, approximate carrying value as a result of their short-term nature. Financial assets measured at amortized cost include cash and trade and other receivables. The fair value of the long-term debt approximates its carrying amount as it has a floating interest rate.

 

Financial liabilities measured at amortized cost include accounts payable and accrued liabilities, long-term debt and lease liability.

 

The Company’s financial instruments are exposed to certain financial risks including credit risk, liquidity risk, currency risk and interest rate risk. There have been no significant changes to those risks impacting the Company since December 31, 2023, nor has there been a significant change in the composition of its financial instruments since December 31, 2023.

 

RELATED PARTY TRANSACTIONS

 

Key management includes the Company’s directors and senior management team. Additional information on the senior management team can be found in the Company’s AIF. The remuneration of directors and the senior management team were as follows:

 

		Three months ended June 30,								Six months ended June 30,
		2024 $				2023 $				2024 $				2023 $
Salaries and employee benefits			673				253				1,023				731
Directors’ fees			69				75				138				156
Share-based compensation			485				577				1,027				1,354
Total			1,227				905				2,188				2,241

 

Executive employment agreements allow for additional payments in the event of a liquidity event, or if the executive is terminated without cause.

 

OUTSTANDING SHARES

 

As at August 8, 2024, the date of this MD&A, the Company had the following securities outstanding:

 

		Number
Common Shares			24,481,835
Share purchase options			1,481,408
Deferred Share Units			75,000
Restricted Share Units			458,895

 

OFF-BALANCE SHEET ARRANGEMENTS

 

The Company has no off-balance sheet arrangements.

 

 

CRITICAL ACCOUNTING POLICIES AND ESTIMATES

 

The preparation of consolidated financial statements in conformity with IFRS Accounting Standards requires management to make estimates and judgements that affect the reported amounts of assets and liabilities at the date of the consolidated financial statements, and the reported amounts of revenue and expenses during the year. Actual results could differ from these estimates. As additional information becomes available or actual amounts are determinable, the recorded estimates are revised and reflected in operating results in the year in which they are determined.

 

Critical accounting policies

 

Revenue

 

To determine revenue recognition for arrangements the Company performs the following five steps: (i) identify the contract(s) with a customer; (ii) identify the performance obligations in the contract; (iii) determine the transaction price; (iv) allocate the transaction price to the performance obligations in the contract; and (v) recognize revenue when (or as) the entity satisfies a performance obligation. The Company only applies the five-step model to contracts when it is probable that the entity will collect the consideration it is entitled to in exchange for the goods or services it transfers to the customer.

 

The Company derives its revenues primarily from the lease and sale of medical devices and the sale of certain one-time-use devices. Capital equipment consists of one-time revenue for the sale of capital equipment including installation fees. Recurring – non-capital revenue consists of the sale of one-time-use devices, lease of medical devices, procedures and services associated with extended warranties. Revenue is recognized when a contractual promise to a customer (performance obligation) has been fulfilled by transferring control over the promised goods or services, generally at the point in time of shipment to or receipt of the products by the customer or when the services are performed. When contracts contain customer acceptance provisions, revenue is recognized on the satisfaction of the specific acceptance criteria.

 

The amount of revenue to be recognized is based on the consideration the Company expects to receive in exchange for its goods and services. For contracts that contain multiple performance obligations, the Company allocates the consideration to which it expects to be entitled to each performance obligation based on relative standalone selling prices and recognizes the related revenue when or as control of each individual performance obligation is transferred to customers.

 

Service revenue related to installation and training is recognized over the period in which the services are performed. Service revenue related to extended warranty service is deferred and recognized on a straight-line basis over the extended warranty period covered by the respective customer contract.

 

Critical accounting estimates

 

Trade and other receivables

 

The key judgements and estimates used in determining the amortized cost for trade and other receivables are the estimated collection period and the discount rate applied to the cash flow projections.

 

DISCLOSURE CONTROLS AND PROCEDURES AND INTERNAL CONTROLS OVER FINANCIAL REPORTING

 

Disclosure controls and procedures have been designed to ensure that information required to be disclosed by the Company is accumulated and communicated to the Company’s management as appropriate to allow timely decisions regarding required disclosure.

 

The Chief Executive Officer and the Chief Financial Officer of the Company (collectively the “Certifying Officers”) are responsible for establishing and maintaining disclosure controls and procedures (“DC&P”) and internal control over financial reporting (“ICFR”), as those terms are defined in National Instrument 52-109 Certification of Disclosure in Issuer’s Annual and Interim Filings.

 

The Certifying Officers have concluded that as at June 30, 2024, the Company's DC&P has been designed effectively to provide reasonable assurance that (a) material information relating to the Company is made known to them by others, particularly during the period in which the annual filings are being prepared; and (b) information required to be disclosed by the Company in its annual filings, interim filings or other reports are filed or submitted, recorded, processed, summarized and reported within the time periods specified in the securities legislation.

 

There have been no significant changes to the Company's ICFR for the period ended June 30, 2024, which have materially affected, or are reasonably likely to materially affect the Company's ICFR. Based on their evaluation of these controls for the period ended June 30, 2024, the Certifying Officers have also concluded that the Company's ICFR have been designed effectively to provide reasonable assurance regarding the reliability of the preparation and presentation of the financial statements for external purposes and that ICFR were effective as at June 30, 2024. The Company used the Committee of Sponsoring Organizations of the Treadway Commission control framework to evaluate DC&P and ICFR.

 

 

It should be noted that while the Company's Certifying Officers believe that the Company's DC&P provides a reasonable level of assurance that they are effective, they do not expect that the disclosure controls will prevent all errors and fraud. A control system, no matter how well conceived or operated, can only provide reasonable, not absolute, assurance that the objectives of the control system are met.

 

ICFR is designed to provide reasonable assurance regarding the reliability of financial reporting and the preparation of the annual financial statements for external reporting purposes in line with IFRS Accounting Standards. Management is responsible for establishing and maintaining adequate internal controls over financial reporting appropriate to the nature and size of the Company. However, any system of internal control over financial reporting has inherent limitations and can only provide reasonable assurance with respect to annual financial statement preparation and presentation.

 

ENVIRONMENTAL, SOCIAL AND GOVERNANCE

 

Environmental, social and governance (“ESG”) issues are an integral part of human life. They’ve also become a more conscious and explicit part of business life, especially for public entities like Profound. The Company believes ESG sensitivities are an integral part of growing a successful, sustainable business. The importance Profound places on ESG principles stems from its foundation as a company, whose mission is focused on providing customizable incision-free therapies that are flexible to treat different types of patients and can treat each patient differently. ESG is embedded in the Company’s corporate strategy, which seeks to maximize long-term value by taking a disciplined and sustainable approach to changing the paradigm of prostate cancer treatment.

 

Through Profound’s ESG plan, the Company intends to create enduring value for shareholders by:

·

attracting, retaining and empowering a diverse, engaged workforce to bring unique perspectives and experiences to strategic decisions;

·

ensuring safe and secure workplaces for its employees and contributing to their welfare;

·

caring for the environment in which the Company operates;

·

strengthening relationships with shareholders by working collaboratively to achieve positive social, economic and environmental outcomes; and

·

operating transparently.

 

Environmental

 

Profound believes in the 3Rs: reduce, reuse, recycle. Profound strives to control the waste and, in its facilities, electronic equipment, paper, glass, plastic and metal items, as well as hazardous waste, are recovered and recycled. Given the finite resources in the world, Profound believes moving towards a circular economy in which Profound reduces waste production is critical for both business and society. Recognizing the opportunity for the medical technology industry to support the transition towards lower waste and circular business models, including by minimizing Profound’s waste footprint and exploring opportunities to reduce the volume of materials used. At Profound, focusing efforts on waste minimization through a repair first strategy, and by using materials that can be recycled to increase the supply of material for future reuse. The equipment that Profound provides to customers is collected, tested, repaired, or refurbished then redeployed thus contributing to a circular economy. Equipment which can no longer be redeployed is brought to organizations or third party vendors that partner with Profound to resell and recycle obsolete equipment.

 

Profound is focused on waste reduction, waste avoidance, and waste management strategies for all materials, including plastic, metal, water and cardboard. To manage the Company’s waste it segregates, recycles, and properly disposes of hazardous and non-hazardous materials and where possible, reuses materials such as alcohol and water through its recycling plan. Profound will continue managing its waste and material use through clear and consistent communication of best practices throughout the Company. Profound is committed to environmental sustainability and prioritizes efforts to prevent pollution and to conserve, recover, and recycle materials wherever possible. The Company attempts to distribute documents electronically to minimize paper consumption, waste and limit the use of single-use plastics. Since 2021, Profound has invested in upgrading its lighting in its manufacturing facilities by retrofitting its lighting to high-efficiency LED to reduce energy consumption and enhance the manufacturing facilities work environment for its employees. The Company plans to continue to invest in lighting where it can have a positive environmental impact and improve working conditions.

 

The repair first approach promotes reuse of existing materials and reduction of new materials (including packaging associated with replacing parts), therefore avoiding waste to landfill. To further support these key areas, the Company is exploring opportunities to recycle glass, water and metals. In Profound’s facilities, multiple waterless urinals have been installed which save over 100,000 litres of water per urinal each year.

 

 

Social

 

As the demand for talent increases, the need for innovative attraction and retention strategies also increases. The Company recognizes that in a rapidly changing environment, its employees are central to its business performance. Profound’s workforce is a key driver of its success, which is why providing a superior employee experience is one of its top priorities. This includes Profound’s commitment to providing a safe and healthy workplace for all employees, consultants, and business partners. Profound does not simply consider this to be its duty of care but an important business practice as it lowers costs, reduces absenteeism and turnover, increases productivity and quality and raises employee morale.

 

In addition to competitive salaries, Profound offers other benefits to its employees. These benefits include a range of incentives, flexible and home-based work options and other health-related benefits. The human resources department is responsible for promoting a wide range of opportunities for innovation at work – which is a significant aspect of Profound’s corporate strategy – and for helping employees to nurture their personal strengths while developing as individuals. In order to be best prepared for challenges, Profound emphasizes the acquisition of technical expertise as part of the qualification system.

 

Diversity and inclusion are long-standing core values that Profound embraces by fostering a respectful workplace where integrity, trust and inclusion are the norm. Profound believes that an inclusive workplace is one where everyone feels a sense of belonging, has a safe environment in which to work and develop, and shares equal opportunities for career advancement regardless of gender, skin colour, ethnicity, religion, age, disability or sexual orientation. Profound values diversity and inclusion as together they enable a highly collaborative and engaging work environment and drive innovation and the development of new ideas, which in turn directly correlates with improved Company performance.

 

Profound wants every employee to feel healthy, safe and productive at work. Cultivating a safe workplace helps advance the Company’s purpose of enabling everyone to live healthier, fuller lives. Given the increased incidence of mental illness in the workplace, Profound’s healthcare coverage offers access to quality counseling services.

 

Artificial intelligence is getting increasingly sophisticated at doing what humans do, but more efficiently, more quickly and at a lower cost. The potential for both AI and robotics in healthcare is vast. Just like in our every-day lives, AI and robotics are increasingly a part of our healthcare eco-system and a major factor for the Company. By analyzing large amounts of data in real time, AI can help improve clinical and nonclinical decision making, ablation planning, treatment time reduction and workflow ease of use optimization. Advances in technology are driving constant changes in the delivery of healthcare. Care providers must seek new training and education opportunities to adjust to this quickly evolving landscape. Artificial intelligence supports these efforts by revolutionizing the capture, storage, and analysis of training video.

 

Artificial intelligence has the potential to help solve some of the biggest challenges facing healthcare today, such as managing costs, physician burnout, and health equity. Our AI solutions are designed to give healthcare professionals the time and tools they need to deliver better care to more people around the world. The thermal boost technology enables predictable, customized ablation at the prostate capsule to ensure a reliable heating of the planned ablation volume. It demonstrates successful application for boosting the MRI-visible lesions to ensure reliable heating to the capsule, boosting in regions with larger prostate radii and boosting if the lethal heat did not initially reach the target boundary.

 

Governance

 

Profound’s Board of Directors are responsible for the stewardship of the Company and for overseeing the conduct of business and the activities of management. The Human Resource and Corporate Governance Committee of the board of directors of Profound is responsible for providing leadership in shaping the Company’s governance policies and practices. The Audit Committee is responsible for overseeing financial reporting and related internal controls, risk, independent and internal auditors, and ethics and compliance. The committees of the board of directors of Profound consist of many affluent senior leadership members within the industry that provide meaningful insight and guidance. Strong and effective governance practices are part of Profound’s organizational culture. This encompasses sound and effective internal processes and procedures, minimizing risks, continuous enhancement of human resource policies and practices, a cyber security strategy and promoting efficiency.

 

The Company holds itself to a high standard of governance and it is continually taking steps to strengthen its performance and accountability in critical areas. Profound’s Code of Business Conduct and Ethics and Whistleblower policies provide the standards for ethical behavior throughout Profound’s business activities and reflect its commitment to conducting a culture of honesty, integrity, and accountability.

 

 

As Profound continues to work towards its mission, the Company is committed to conducting its business in a responsible and sustainable manner by aspiring to develop healthy, resilient communities through its dedication to social, economic and environmental sustainability. By unlocking value through its core activities, Profound remains focused on execution on all fronts including in fulfilling its commitment to ESG best practices in the years to come.

 

RISK FACTORS

 

For a detailed description of risk factors associated with the Company, refer to the “Risk Factors” section of the AIF, which is available on SEDAR+ at www.sedarplus.ca and filed as an exhibit to the 40-F, available on EDGAR at www.sec.gov.

 

In addition, the Company is exposed to a variety of financial risks in the normal course of operations, including risks relating to cash flows from operations, liquidity, capital reserves, market rate fluctuations and internal controls over financial reporting. Profound’s overall risk management program and business practices seek to minimize any potential adverse effects on the Company’s consolidated financial performance. Financial risk management is carried out under practices approved by Profound’s audit committee. This includes reviewing and making recommendations to the board of directors regarding the adequacy of the Company’s risk management policies and procedures with regard to identification of the Company’s principal risks, and implementation of appropriate systems and controls to manage these risks.

 

ADDITIONAL INFORMATION

 

Additional information relating to the Company, including the AIF the other exhibits to the 40-F, is available on SEDAR+ at www.sedarplus.ca and on EDGAR at www.sec.gov. The Common Shares are listed for trading on the TSX under the symbol “PRN” and on Nasdaq under the symbol “PROF”.

 

 

 

Page 23

 

Exhibit 99.4

FORM 52-109F2
CERTIFICATION OF INTERIM FILINGS
FULL CERTIFICATE

 

 

 

I, Arun Menawat, the Chief Executive Officer of Profound Medical Corp., certify the following:

 

1.

Review: I have reviewed the interim financial report and interim MD&A (together, the “interim filings”) of Profound Medical Corp. (the “issuer”) for the interim period ended June 30, 2024.

 

2.

No misrepresentations: Based on my knowledge, having exercised reasonable diligence, the interim filings do not contain any untrue statement of a material fact or omit to state a material fact required to be stated or that is necessary to make a statement not misleading in light of the circumstances under which it was made, with respect to the period covered by the interim filings.

 

3.

Fair presentation: Based on my knowledge, having exercised reasonable diligence, the interim financial report together with the other financial information included in the interim filings fairly present in all material respects the financial condition, financial performance and cash flows of the issuer, as of the date of and for the periods presented in the interim filings.

 

4.

Responsibility: The issuer’s other certifying officer(s) and I are responsible for establishing and maintaining disclosure controls and procedures (DC&P) and internal control over financial reporting (ICFR), as those terms are defined in National Instrument 52-109 Certification of Disclosure in Issuers’ Annual and Interim Filings, for the issuer.

 

5.

Design: Subject to the limitations, if any, described in paragraphs 5.2 and 5.3, the issuer’s other certifying officer(s) and I have, as at the end of the period covered by the interim filings

 

(a)

designed DC&P, or caused it to be designed under our supervision, to provide reasonable assurance that

 

(i)

material information relating to the issuer is made known to us by others, particularly during the period in which the interim filings are being prepared; and

 

(ii)

information required to be disclosed by the issuer in its annual filings, interim filings or other reports filed or submitted by it under securities legislation is recorded, processed, summarized and reported within the time periods specified in securities legislation; and

 

(b)

designed ICFR, or caused it to be designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with the issuer’s GAAP.

 

5.1

Control framework: The control framework the issuer’s other certifying officer(s) and I used to design the issuer’s ICFR is the Internal Control – Integrated Framework (2013) issued by the Committee of Sponsoring Organizations of the Treadway Commission (COSO).

 

5.2

ICFR – material weakness relating to design: N/A

 

5.3

Limitation on scope of design: N/A

 

6.

Reporting changes in ICFR: The issuer has disclosed in its interim MD&A any change in the issuer’s ICFR that occurred during the period beginning on April 1, 2024 and ended on June 30, 2024 that has materially affected, or is reasonably likely to materially affect, the issuer’s ICFR.

 

Date: August 8, 2024

 

_(signed) Arun Menawat_
Arun Menawat
Chief Executive Officer

 

Exhibit 99.5

 

FORM 52-109F2
CERTIFICATION OF INTERIM FILINGS
FULL CERTIFICATE

 

I, Rashed Dewan, Chief Financial Officer of Profound Medical Corp., certify the following:

 

1.

Review: I have reviewed the interim financial report and interim MD&A (together, the “interim filings”) of Profound Medical Corp. (the “issuer”) for the interim period ended June 30, 2024.

 

2.

No misrepresentations: Based on my knowledge, having exercised reasonable diligence, the interim filings do not contain any untrue statement of a material fact or omit to state a material fact required to be stated or that is necessary to make a statement not misleading in light of the circumstances under which it was made, with respect to the period covered by the interim filings.

 

3.

Fair presentation: Based on my knowledge, having exercised reasonable diligence, the interim financial report together with the other financial information included in the interim filings fairly present in all material respects the financial condition, financial performance and cash flows of the issuer, as of the date of and for the periods presented in the interim filings.

 

4.

Responsibility: The issuer’s other certifying officer(s) and I are responsible for establishing and maintaining disclosure controls and procedures (DC&P) and internal control over financial reporting (ICFR), as those terms are defined in National Instrument 52-109 Certification of Disclosure in Issuers’ Annual and Interim Filings, for the issuer.

 

5.

Design: Subject to the limitations, if any, described in paragraphs 5.2 and 5.3, the issuer’s other certifying officer(s) and I have, as at the end of the period covered by the interim filings

 

(a)

designed DC&P, or caused it to be designed under our supervision, to provide reasonable assurance that

 

(i)

material information relating to the issuer is made known to us by others, particularly during the period in which the interim filings are being prepared; and

 

(ii)

information required to be disclosed by the issuer in its annual filings, interim filings or other reports filed or submitted by it under securities legislation is recorded, processed, summarized and reported within the time periods specified in securities legislation; and

 

(b)

designed ICFR, or caused it to be designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with the issuer’s GAAP.

 

5.1

Control framework: The control framework the issuer’s other certifying officer(s) and I used to design the issuer’s ICFR is the Internal Control – Integrated Framework (2013) issued by the Committee of Sponsoring Organizations of the Treadway Commission (COSO).

 

5.2

ICFR – material weakness relating to design: N/A

 

5.3

Limitation on scope of design: N/A

 

6.

Reporting changes in ICFR: The issuer has disclosed in its interim MD&A any change in the issuer’s ICFR that occurred during the period beginning on April 1, 2024 and ended on June 30, 2024 that has materially affected, or is reasonably likely to materially affect, the issuer’s ICFR.

 

Date: August 8, 2024

_(signed) Rashed Dewan_
Rashed Dewan
Chief Financial Officer

 

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