TORONTO, Aug. 14,
2023 /CNW/ - MediPharm Labs Corp. (TSX: LABS) (OTCQB:
MEDIF) (FSE: MLZ) ("MediPharm", "MediPharm Labs" or the "Company")
a pharmaceutical company specialized in precision-based
cannabinoids, today announced its financial results for the three
months ended June 30, 2023.
Second Quarter 2023 – Select Highlights
- Completed our first commercial delivery to the United States. The delivery was comprised
of clinical trial material for a fully funded large-scale phase two
clinical trial.
- On April 1st, 2023,
MediPharm closed the acquisition of VIVO Cannabis Inc. ("VIVO") in
an all equity business combination.
- Revenue has doubled versus prior year with the incorporation of
VIVO.
- Gross profit was positive for the third consecutive quarter.
Largest Adjusted Gross Profit increase in company history and best
adjusted gross profit since Q4 2019 at approximately 21%
- Successful integration of VIVO, including executing a
restructuring and cost savings program that will save approximately
$7M on an annualized basis as we
progress towards our previously communicated synergy target of
$7-$9M.
(2)(3)(4)(5)
- Adjusted EBITDA(1) of negative $3.2M, and improvement of $3.2M or 50% versus Q2 2022 and remained
consistent with Q1 2023 despite the incorporation of VIVO which
historically had an Adjusted EBITDA(1) of negative
$2M per quarter.
- Strong balance sheet, relative to our peers, with $14.7M of cash, less than $3M of debt and a plan to generate cash in the
near term.
Continued Progress Solidifying Leadership in Cannabis-Based
Pharmaceutical Industry
- Subsequent to the quarter, on July 28,
2023, the Company completed its first delivery of cannabis
clinical trial material to a US research partner. The delivery of
pharmaceutical cannabis product was for a National Institute of
Health funded clinical trial, following receipt of an import permit
from the US Drug Enforcement Agency (DEA) and Health Canada export
permit.
- The Company has provided a full response to the US Food and
Drug Administration (FDA) in relation to the initial foreign drug
site inspection of its Barrie facility regarding a new Drug Master
File (DMF) being referenced in a recent Abbreviated New Drug
Application (ANDA). This is the first US FDA Audit of a
purpose-built commercial cannabis facility in Canada. MediPharm continues in-depth
correspondence with the FDA regarding its November 2022 on-site inspection related to Drug
Master File being submitted as part of an Abbreviated New Drug
Application (ANDA) submission by an international pharmaceutical
partner.
Tremendous Growth in Medical Cannabis
- The Canadian Medical Cannabis revenue for Q2 2023 was
$3.8M versus $0.2M in Q2 2022 and $0.6M in Q1 2023 driven by the integration of the
VIVO medical channel, Canna Farms.
- Canna Farms has serviced patients since 2013 and is a top-ten
medical channel in Canada. Since
the transaction Canna Farms has listed MediPharm products for sale
direct to patient. This synergy creates better margin where
MediPharm produces these products at higher volume or were being
purchased by third party manufacturing. It also assists in patient
recruitment and retention as we are able to provide additional
selection and more standardized medical products.
- International Medical revenue in Q2 2023 was $3.0M versus $0.9M
in Q2 2022 and $1.8M in Q1 2023
representing a 249% and 66% growth respectively. The growth of
International Medical was largely driven by the integration of
VIVO's Australian business, Beacon Medical Australia.
- The Beacon Medical Australia flower portfolio is currently the
number three flower brand by sales and continues to have year over
year growth in pharmacy patient sales. The Company has prepared for
our launch of Beacon Medical oil and vapes. It is anticipated these
new high margin products will have the same success as their flower
counterparts.
- In July 2023, the Company entered
into an additional supply agreement with a top tier generic
pharmaceutical company in Brazil.
Under the agreement, the customer will apply to the Brazilian
Health Regulatory Agency for a number of cannabis product
approvals. MediPharm has received similar approvals in Brazil with other pharma customers. It is
anticipated the delivery of additional products could begin in Q1
2024, and substantially increase the current Brazilian revenue.
(2)
Progress Towards Profitability
- Revenue for Q2 2023 of $9.6
million increased approximately 120% versus Q2 2022 and 64%
versus Q1 2023 despite the seasonality of the Canadian Adult use
and Wellness market.
- Q2 2023 gross profit was $0.8M/8.1% and was impacted by several discrete
items including inventory write-downs, fair value adjustments, and
severance for restructuring. Adjusting for these items gross margin
was approximately 21%. This is the third consecutive quarter of
positive gross profit. Gross profit continues to improve, driven by
product mix, production efficiencies and cost reductions.
Management continues to focus on efficiencies to drive gross
profit.
- Total Opex, which includes G&A, Marketing and selling and
R&D expenses was $7.5M in the
quarter. Adjusting for severance and some other discrete items,
normalized Opex was approximately $6.5M which includes $2.3M from the incorporation of VIVO.
Retrospectively, if VIVO were included in our Q2 2022 results, Opex
in Q2 2023 is down approximately 35% or $3.7M.
Solid Balance Sheet
- MediPharm ended Q2 2023 with $14.7M in cash and cash equivalents with
approximately $3M of debt. This
financial position is expected to give MediPharm longevity to
execute on its short-term sales plans and provides the balance
sheet strength to support the Company's long-term growth strategy.
In addition, we expect that the Company's favourable summary
judgement, now scheduled in front of the Court of Appeal for
October 12, 2023, will strengthen the
Company's balance sheet going forward. In addition, the Company has
real estate assets held for sale with the ability to generate cash
of approximately $2M to $3M in the near term. (2)
Management Commentary
David Pidduck, CEO, MediPharm
Labs commented, "We are very happy with our Q2 performance
lead by the smooth VIVO integration that is ahead of all cost
synergy targets. We are excited to have new employees, new business
units, new products and capabilities and new investors and
stakeholders."
Greg Hunter, CFO, MediPharm Labs
added, "In Q2, we continued to make progress by growing our revenue
base, improving gross margins, reducing expenses and reducing cash
burn as we drive towards profitability. We have also demonstrated
that we can quickly integrate and drive synergies through
acquisitions."
Financial Summary
|
Three months
ended
|
|
|
June 30,
2023
$'000s
|
|
March 31,
2023
$'000s
|
December
31, 2022
$'000s
|
September
30, 2022
$'000s
|
June 30,
2022
$'000s
|
Revenue
|
9,583
|
|
5,843
|
5,616
|
7,262
|
4,362
|
Gross profit
|
855
|
|
387
|
211
|
(1,190)
|
(532)
|
Opex(a)
|
(7,516)
|
|
(2,923)
|
(5,122)
|
(5,444)
|
(6,607)
|
Adjusted
EBITDA(b)
|
(3,191)
|
|
(3,090)
|
(3,634)
|
(4,974)
|
(6,345)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
(a)
|
Opex includes general
administrative expense, marketing and selling expenses and R&D
expenses.
|
(b)
|
Adjusted EBITDA is a
non-IFRS measure. See "Non-IFRS Measures".
|
Q2 2023 Financial Results Conference Call
MediPharm's executive management team will also host a
conference call and audio webcast on Monday,
August 14, 2023 at 8:30 a.m. eastern
time to discuss the Company's financial results.
Conference Call:
Toll-free number: +1 (888) 330-2454 / International number: +1
(240) 789-2714
Conference ID: 4921762
Participants are asked to dial in approximately 15 minutes
before the start of the call.
Audio Webcast:
An audio webcast will be available by visiting the following
link here.
For those who are unable to participate on the live conference
call or webcast, a replay will be available at
https://www.medipharmlabs.com/investors approximately one day after
completion of the call.
About MediPharm Labs
Founded in 2015, MediPharm Labs specializes in the development
and manufacture of purified, pharmaceutical-quality cannabis
concentrates, active pharmaceutical ingredients (API) and advanced
derivative products utilizing a Good Manufacturing Practices
certified facility with ISO standard-built clean rooms. MediPharm
Labs has invested in an expert, research driven team,
state-of-the-art technology, downstream purification methodologies
and purpose built facilities with five primary extraction lines for
delivery of pure, trusted and precision-dosed cannabis products for
its customers. Through its wholesale and white label platforms,
MediPharm Labs formulates, develops (including through sensory
testing), processes, packages and distributes cannabis extracts and
advanced cannabinoid-based products to domestic and international
markets.
In 2021, MediPharm Labs received a Pharmaceutical Drug
Establishment Licence from Health Canada, becoming the only company
in North America to hold a
domestic Good Manufacturing Licence for the extraction of natural
cannabinoids. The Company carries out its operations in compliance
with all applicable laws in the countries in which it operates.
In 2023, MediPharm acquired VIVO Cannabis Inc. which expanded
MediPharm's reach to medical patients in Canada via Canna Farms medical ecommerce
platform, and in Australia and
Germany through Beacon Medical PTY
and Beacon Medical GMBH. This acquisition also included Harvest
Medical Clinics in Canada which
provides medical cannabis patients with physician consultations for
medical cannabis education and prescription.
Notes:
|
|
(1)
|
This is a non-IFRS
reporting measure. See "Non-IFRS Measures" below.
|
(2)
|
This is forward-looking
information and based on a number of assumptions. See "Cautionary
Note Regarding Forward-Looking Information" and
"Assumptions".
|
(3)
|
Based on both costs and
revenue opportunities identified by MediPharm and VIVO management.
Revenue opportunity assumed that both existing products may be sold
into the existing sales channels of both VIVO and MediPharm. Costs
savings estimated depends on the eliminating duplicated public
company expenses and redundant corporate infrastructure.
|
(4)
|
This target, and the
related assumptions, involve known and unknown risks and
uncertainties that may cause actual results to differ materially.
While MediPharm and VIVO believe there is a reasonable basis for
this target, such target may not be met. Actual results may vary
and differ materially from the targets. See
"Assumptions".
|
(5)
|
Certain financial
information included in this press release is neither audited nor
reviewed. Where possible, the information has been constructed by
management from available audited or audit reviewed financial
statements. Where no audited or audit reviewed information has been
available, additional management accounting information has been
utilized to construct financial information. Readers are cautioned
not to place undue reliance on such information.
|
Assumptions
In developing the financial guidance set forth above, MediPharm
and VIVO made the following assumptions and relied on the following
factors and considerations:
- The targets are based on MediPharm and VIVO's historical
results including annualized revenue from its interim financial
results for the period ended September 30,
2022, as adjusted for subsequent events including completion
of the Transaction with VIVO.
- Revenue sustainability and growth depend on a variety of
factors, including among other things, location, competition, legal
and regulatory requirements. Prices are projected forward at
recently realized wholesale and direct to patient prices.
- Cost of goods sold, before taking into account the impact of
value changes in biological assets (which are non-cash in nature),
and, accordingly, are excluded from calculations of EBITDA, have
been projected based on estimated costs of production and capacity
available from a similar supply chain.
- The immediate reduction of public company professional and
service fees, such as but not limited to, errors and omissions
insurance, audit services, listing expenses and external legal
fees.
- Implied redundancy of employee roles in the Company, mainly in
corporate functions. Impacted employee severance fees are
calculated on current employment agreements and Employment
Standards Act (Ontario).
- No changes to existing medical cannabis legislation and
regulations in Canada,
Germany, Australia and Brazil.
- All VIVO and MediPharm regulatory licenses remain in good
standing with domestic and international regulators, particular
Good Manufacturing Practices (GMP).
Non-IFRS Measures
This press release contains references to "EBITDA", "Adjusted
EBITDA" and "Adjusted Gross Profit", which are non-IFRS financial
measures. Management believes that these supplementary non-IFRS
financial measures provide useful additional information related to
the operating results of the Company. These non-IFRS financial
measures are not recognized under IFRS and, accordingly, users are
cautioned that these measures should not be construed as
alternatives to net income (loss) and gross profit determined in
accordance with IFRS as measures of profitability or as
alternatives to the Company's IFRS-based Financial Statements. The
non-IFRS measures presented may not be comparable to similar
measures presented by other issuers. EBITDA refers to earnings
before interest, taxes, depreciation, and amortization and is used
as an indicator of the Company's overall profitability. Adjusted
EBITDA is a measure of the Company's overall financial performance
and is used as an alternative to earnings or income in some
circumstances. Adjusted EBITDA is essentially net income (loss)
with interest, taxes, depreciation and amortization, non-cash
adjustments and other unusual or non-recurring items added back.
Adjusted EBITDA has limitations as an analytical tool as it does
not include depreciation and amortization expense, fair value
adjustments for biological assets, interest income and expense,
finance fees, gain in revaluation of derivative liabilities, taxes,
government grants including rent and wage subsidies, one-off
transactions, impairment losses on inventory and on fixed assets
and intangibles, write down of deposits and share-based
compensation. Because of these limitations, Adjusted EBITDA should
not be considered as the sole measure of the Company's performance
and should not be considered in isolation from, or as a substitute
for, analysis of the Company's results as reported under IFRS.
Adjusted EBITDA, as used within the Company's disclosure, may not
be directly comparable to Adjusted EBITDA used by other reporting
issuers. Adjusted Gross Profit refers to gross profit
excluding the adjustments for accelerated depreciation, write down
of non-current deposits, fair value adjustments for biological
assets, severance for restructuring and write down of inventory and
other one-off transactions. Adjusted Gross Profit is a useful
measure as it represents gross profit for management purposes based
on costs to manufacture, package and ship inventory sold, exclusive
of any impairments due to changes in internal or external
influences. Adjusted EBITDA and Adjusted Gross Profit do not have
any standardized meanings and the Company's method of calculating
such non-IFRS measures may not be comparable to calculations used
by other companies bearing the same description. See "Use of
Non-IFRS Measures" in the Company's management's discussion and
analysis for the period ended March 31, 2023 for
additional information.
Cautionary Note Regarding Forward-Looking Information
This news release contains "forward-looking information" and
"forward-looking statements" (collectively, "forward-looking
statements") within the meaning of the applicable Canadian
securities legislation. All statements, other than statements of
historical fact, are forward-looking statements and are based on
expectations, estimates and projections as at the date of this news
release. Any statement that involves discussions with respect to
predictions, expectations, beliefs, plans, projections, objectives,
assumptions, future events or performance (often but not always
using phrases such as "expects", or "does not expect", "is
expected", "anticipates" or "does not anticipate", "plans",
"budget", "scheduled", "forecasts", "estimates", "believes" or
"intends" or variations of such words and phrases or stating that
certain actions, events or results "may" or "could", "would",
"might" or "will" be taken to occur or be achieved) are not
statements of historical fact and may be forward-looking
statements. In this news release, forward-looking statements relate
to, among other things, statements regarding: the Company's
progress toward profitability; potential annualized savings to be
realized as a result of the Transaction and the Company's
restructuring efforts; the anticipated timing and results of
integration efforts of the Company following completion of the
Transaction; potential cost synergies to be realized as a result of
the Transaction; results of Investigational New Drug applications
submitted to the FDA by US-based research partners; and revenue
growth. Forward-looking statements are necessarily based upon a
number of estimates and assumptions that, while considered
reasonable, are subject to known and unknown risks, uncertainties,
and other factors which may cause the actual results and future
events to differ materially from those expressed or implied by such
forward-looking statements. Such factors include, but are not
limited to: general business, economic, competitive, political and
social uncertainties; the inability of MediPharm to obtain adequate
financing; the delay or failure to receive regulatory approvals;
and other factors discussed in MediPharm's filings, available on
the SEDAR website at www.sedar.com. There can be no assurance
that such 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 the forward-looking statements and information
contained in this news release. Except as required by law,
MediPharm assumes no obligation to update the forward-looking
statements of beliefs, opinions, projections, or other factors,
should they change.
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SOURCE MediPharm Labs Corp.