false000199470200019947022024-08-122024-08-12

 

UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549

 

FORM 8-K

 

CURRENT REPORT

Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934

Date of Report (Date of earliest event reported): August 12, 2024

 

 

Kyverna Therapeutics, Inc.

(Exact name of Registrant as Specified in Its Charter)

 

 

Delaware

001-41947

83-1365441

(State or Other Jurisdiction
of Incorporation)

(Commission File Number)

(IRS Employer
Identification No.)

 

 

 

 

 

5980 Horton St., STE 550

 

Emeryville, California

 

94608

(Address of Principal Executive Offices)

 

(Zip Code)

 

Registrant’s Telephone Number, Including Area Code: (510) 925-2492

 

N/A

(Former Name or Former Address, if Changed Since Last Report)

 

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:

Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

Securities registered pursuant to Section 12(b) of the Act:


Title of each class

 

Trading
Symbol(s)

 


Name of each exchange on which registered

Common Stock, par value $0.00001 per share

 

KYTX

 

The Nasdaq Stock Market LLC

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§ 230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§ 240.12b-2 of this chapter).

Emerging growth company

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.

 


Item 2.02 Results of Operations and Financial Condition.

On August 12, 2024, Kyverna Therapeutics, Inc. (the “Company”) issued a press release providing a business update and reporting financial results for the quarter ended June 30, 2024. A copy of the press release is furnished as Exhibit 99.1 to this Current Report on Form 8-K (the “Current Report”).

 

In accordance with General Instructions B.2 of Form 8-K, the information in Item 2.02 of this Current Report and Exhibit 99.1 hereto, shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liability of that section, and shall not be incorporated by reference into any registration statement or other document filed under the Securities Act of 1933, as amended (the “Securities Act”), or the Exchange Act, except as shall be expressly set forth by specific reference in such filing.

Item 9.01 Financial Statements and Exhibits.

(d) Exhibits

 

Exhibit

Number

Description

99.1

 

Press Release issued by Kyverna Therapeutics, Inc. dated August 12, 2024.

 

 

 


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 hereunto duly authorized.

KYVERNA THERAPEUTICS, INC.

Date: August 12, 2024

By:

/s/ Peter Maag, Ph.D.

Peter Maag, Ph.D.

Chief Executive Officer

 


 

 

Exhibit 99.1

 

Kyverna Therapeutics Provides Business Update and Reports Second Quarter 2024 Financial Results

 

Actively recruiting clinical trials in neurology and rheumatology with KYV-101
No severe ICANS or CRS reported in first 36 autoimmune disease patients treated with KYV-101
Received FDA RMAT Designation for KYV-101 for treatment of patients with Stiff-Person Syndrome
Received FDA RMAT Designation for KYV-101 for treatment of patients with Myasthenia Gravis
Reported clinical experience with first KYV-101 patient disease-free at 1 year after treatment

 

EMERYVILLE, Calif., August 12, 2024 – Kyverna Therapeutics, Inc. (Nasdaq: KYTX), a patient-centered, clinical-stage biopharmaceutical company focused on developing cell therapies for patients suffering from autoimmune diseases, today reported its business highlights and financial results for the second quarter ended June 30, 2024.

 

“We have shown promising initial safety and efficacy for our lead product candidate, KYV-101, and continue to lead the way in bringing CAR T-cell therapies to patients with autoimmune diseases in the US and Europe,” said Peter Maag, Chief Executive Officer of Kyverna. “We believe that KYV-101 brings the power of CD19-directed CAR T therapy to deliver deep tissue-based B cell depletion using a fully human CAR and CD28 costimulatory domain designed by the NIH to improve tolerability. We look forward to sharing more clinical data throughout the rest of 2024 as we strive to fulfill our promise to bring hope to patients living with autoimmune disorders.”

 

Second Quarter 2024 and Recent Business Highlights

Presented clinical data showing use of the CAR in KYV-101 across 50 patients including 15 different autoimmune conditions at CAR T centers in the US and Europe
Expanded KYV-101 safety experience with no severe ICANS or CRS Grade ≥3 reported in 36 autoimmune patients treated as of July 31, 2024, using CAR construct designed by the NIH to improve tolerability
Received two U.S. FDA Regenerative Medicine Advanced Therapy (RMAT) Designations for KYV-101: one for the treatment of patients with Stiff-Person Syndrome, and one for the treatment of patients with myasthenia gravis, building on the emerging body of clinical evidence
Achieved 100% manufacturing success rate across all 36 cumulative autoimmune patients treated with KYV-101 as of July 31, 2024
Reported clinical experience of a myasthenia gravis patient who is now free of disease one year after treatment with KYV-101
Progressed the global KYSA clinical trial program in multiple indications across rheumatology and neurology: Phase 1/2 trials in lupus nephritis (KYSA-1 and KYSA-3), a Phase 1/2 trial in systemic sclerosis (KYSA-5), a Phase 2 trial in myasthenia gravis (KYSA-6), a Phase 2 trial in multiple sclerosis (KYSA-7), and a Phase 2 trial in stiff-person syndrome (KYSA-8)

 

Upcoming Milestones

Neurology case reports at ECTRIMS in September 2024
Rheumatology KYSA Clinical Trial updates at ACR in November 2024
Guidance on anticipated regulatory phase transitions in 2025, following RMAT meetings with the FDA

 

Financial Results for the Quarter Ended June 30, 2024

For the quarter ended June 30, 2024, the company reported a net loss of $28.8 million, or a net loss per common share of $0.67, compared to a net loss of $13.1 million, or a net loss per common share of $20.86, for the same period in 2023.

 

During the six months ended June 30, 2024, net cash used in operating activities was $49.7 million, compared to $22.7 million for the same period in 2023.

 

Kyverna reported $346.2 million in cash, cash equivalents, and available-for-sale marketable securities as of June 30, 2024.

 

 

 

About Kyverna Therapeutics

 


 

Kyverna is a patient-centered, clinical-stage biopharmaceutical company focused on developing cell therapies for patients suffering from autoimmune diseases.

 

Our lead CAR T-cell therapy candidate, KYV-101 is advancing through clinical development with sponsored clinical trials across two broad areas of autoimmune disease: rheumatology and neurology, including Phase 2 trials for multiple sclerosis, myasthenia gravis and stiff-person syndrome, a Phase 1/2 trial for systemic sclerosis, and two ongoing multi-center, open-label Phase 1/2 trials in the United States and Germany for patients with lupus nephritis.

 

Kyverna's pipeline includes next-generation chimeric antigen receptor (CAR) T-cell therapies in both autologous and allogeneic formats with properties intended to be well suited for use in B cell-driven autoimmune diseases. For more information, please visit www.kyvernatx.com.

 

Forward-looking Statements

This press release contains forward looking statements that are based on management’s beliefs and assumptions and on information currently available to management of Kyverna Therapeutics, Inc. (“Kyverna”, “we”, “our,” or the “Company”). All statements other than statements of historical facts contained in this press release are forward looking statements. Forward looking statements include, but are not limited to, statements concerning: the Company’s future results of operations and financial position, business strategy, drug candidates, planned preclinical studies and clinical trials, results of preclinical studies and named patient activities, ongoing clinical trials, research and development costs, plans for manufacturing, regulatory approvals, timing and likelihood of success, as well as plans and objectives of management for future operations. These forward-looking statements are subject to risks and uncertainties, including the factors described under the Risk Factors section of the Company’s Annual Report on Form 10-K for the year ended December 31, 2023 filed with the SEC on March 26, 2024 and any subsequent Quarterly Reports on Form 10-Q filed by the Company. Actual results could differ materially and adversely from those anticipated or implied in the forward looking statements. When evaluating Kyverna’s business and prospects, careful consideration should be given to these risks and uncertainties. These statements speak only as of the date of this press release, and Kyverna undertakes no obligation to update or revise these statements.

 

 

For more information, please contact:

Investor Contact:

George Thampy

Kyverna Therapeutics

InvestorRelations@kyvernatx.com

 

Media Contact:

Consort Partners for Kyverna

kyvernatx@consortpartners.com

 

 

 

 


 

Kyverna Therapeutics, Inc.

Condensed Statements of Operations and Comprehensive Loss

(in thousands, except share and per share data)

(unaudited)

 

 

 

Three Months Ended June 30,

 

 

Six Months Ended June 30,

 

 

 

2024

 

 

2023

 

 

2024

 

 

2023

 

Operating expenses

 

 

 

 

 

 

 

 

 

 

 

 

Research and development

 

$

27,321

 

 

$

10,405

 

 

$

49,797

 

 

$

19,116

 

General and administrative

 

 

6,114

 

 

 

2,897

 

 

 

12,996

 

 

 

5,631

 

Total operating expenses

 

 

33,435

 

 

 

13,302

 

 

 

62,793

 

 

 

24,747

 

Loss from operations

 

 

(33,435

)

 

 

(13,302

)

 

 

(62,793

)

 

 

(24,747

)

Interest income

 

 

4,694

 

 

 

264

 

 

 

7,429

 

 

 

613

 

Interest expense

 

 

(39

)

 

 

(46

)

 

 

(83

)

 

 

(90

)

Other expense, net

 

 

(23

)

 

 

(7

)

 

 

(49

)

 

 

(10

)

Total other income, net

 

 

4,632

 

 

 

211

 

 

 

7,297

 

 

 

513

 

Net loss

 

 

(28,803

)

 

 

(13,091

)

 

 

(55,496

)

 

 

(24,234

)

Other comprehensive (loss) gain

 

 

 

 

 

 

 

 

 

 

 

 

Unrealized (loss) gain on available-for-sale marketable securities, net

 

 

(36

)

 

 

8

 

 

 

(41

)

 

 

26

 

Total other comprehensive (loss) gain

 

 

(36

)

 

 

8

 

 

 

(41

)

 

 

26

 

Net loss and other comprehensive loss

 

$

(28,839

)

 

$

(13,083

)

 

$

(55,537

)

 

$

(24,208

)

Net loss per share attributable to common stockholders, basic and diluted

 

$

(0.67

)

 

$

(20.86

)

 

$

(1.66

)

 

$

(40.40

)

Weighted-average shares of common stock outstanding, basic and diluted

 

 

43,125,709

 

 

 

627,589

 

 

 

33,439,886

 

 

 

599,917

 

 

 

 

 

 

 


 

Kyverna Therapeutics, Inc.

Condensed Balance Sheets

(in thousands, except share and per share data)

(unaudited)

 

 

 

June 30,

 

 

December 31,

 

 

 

2024

 

 

2023

 

Assets

 

 

 

 

 

 

Current assets

 

 

 

 

 

 

Cash and cash equivalents

 

$

131,618

 

 

$

34,647

 

Available-for-sale marketable securities

 

 

214,619

 

 

 

22,896

 

Prepaid expenses and other current assets

 

 

2,586

 

 

 

3,121

 

Total current assets

 

 

348,823

 

 

 

60,664

 

Restricted cash

 

 

574

 

 

 

565

 

Property and equipment, net

 

 

3,366

 

 

 

2,326

 

Operating lease right-of-use assets

 

 

7,825

 

 

 

6,494

 

Finance lease right-of-use assets

 

 

1,315

 

 

 

1,790

 

Other non-current assets

 

 

1,213

 

 

 

3,356

 

Total assets

 

$

363,116

 

 

$

75,195

 

Liabilities, redeemable convertible preferred stock and stockholders’
   equity (deficit)

 

 

 

 

 

 

Current liabilities

 

 

 

 

 

 

Accounts payable

 

$

4,861

 

 

$

4,358

 

Accrued compensation

 

 

2,722

 

 

 

2,812

 

Accrued license expense – related party

 

 

6,250

 

 

 

6,250

 

Other accrued expenses and current liabilities

 

 

5,775

 

 

 

3,519

 

Operating lease liabilities, short-term portion

 

 

2,867

 

 

 

1,964

 

Finance lease liabilities, short-term portion

 

 

1,003

 

 

 

956

 

Total current liabilities

 

 

23,478

 

 

 

19,859

 

Operating lease liabilities, net of short-term portion

 

 

5,722

 

 

 

5,238

 

Finance lease liabilities, net of short-term portion

 

 

407

 

 

 

921

 

Total liabilities

 

 

29,607

 

 

 

26,018

 

Commitments and contingencies

 

 

 

 

 

 

Redeemable convertible preferred stock, no par value; no shares authorized, issued and outstanding as of June 30, 2024; $0.00001 par value, 114,556,997 shares authorized as of December 31, 2023; 114,556,997 shares issued and outstanding as of December 31, 2023; liquidation preference of $181,273 as of December 31, 2023

 

 

 

 

 

180,574

 

Stockholders’ equity (deficit)

 

 

 

 

 

 

Preferred stock, 10,000,000 shares authorized, $0.00001 par value, no shares issued and outstanding as of June 30, 2024; no shares authorized, issued, and outstanding as of December 31, 2023

 

 

 

 

 

 

Common stock, $0.00001 par value; 490,000,000 and 140,492,016 shares authorized as of June 30, 2024 and December 31, 2023, respectively; 43,146,852 and 1,250,103 shares issued and outstanding as of June 30, 2024 and December 31, 2023, respectively

 

 

 

 

 

 

Additional paid-in capital

 

 

525,085

 

 

 

4,642

 

Accumulated other comprehensive (loss) income

 

 

(37

)

 

 

4

 

Accumulated deficit

 

 

(191,539

)

 

 

(136,043

)

Total stockholders’ equity (deficit)

 

 

333,509

 

 

 

(131,397

)

Total liabilities, redeemable convertible preferred stock and
   stockholders’ equity (deficit)

 

$

363,116

 

 

$

75,195

 

 

 

 

 

 

 


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Aug. 12, 2024
Cover [Abstract]  
Document Type 8-K
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Document Period End Date Aug. 12, 2024
Entity Registrant Name Kyverna Therapeutics, Inc.
Entity Central Index Key 0001994702
Entity Emerging Growth Company true
Entity File Number 001-41947
Entity Incorporation, State or Country Code DE
Entity Tax Identification Number 83-1365441
Entity Address, Address Line One 5980 Horton St., STE 550
Entity Address, City or Town Emeryville
Entity Address, State or Province CA
Entity Address, Postal Zip Code 94608
City Area Code (510)
Local Phone Number 925-2492
Entity Information, Former Legal or Registered Name N/A
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Soliciting Material false
Pre-commencement Tender Offer false
Pre-commencement Issuer Tender Offer false
Entity Ex Transition Period false
Title of 12(b) Security Common Stock, par value $0.00001 per share
Trading Symbol KYTX
Security Exchange Name NASDAQ

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