MediPharm Labs Corp. (TSXV: LABS) (OTCQB: MLCPF) (FSE: MLZ)
(“MediPharm Labs” or the “Company”) a global leader in specialized,
research-driven cannabis extraction, distillation, purification and
cannabinoid isolation, is pleased to announce fourth quarter and
full year financial results for the year ended December 31, 2018.
The audited consolidated financial statements and management's
discussion and analysis for the periods are available on SEDAR.
Fourth Quarter 2018
Highlights
- Revenue of $10.2 million, commencing November 12th after
receipt of sales license from Health Canada
- Gross Profit of $4.0 million, Gross Margin 39%
- Adjusted EBITDA(1) of $2.1 million, Adjusted EBITDA(1) margin
of 21%
- Became first fully Licensed Producer to specialize solely in
cannabis extraction
- Signed large private label cannabis oil sale agreement with
Canopy Growth Corporation for the sale of up to 900 kg over 18
months
- Expanded licensed extraction throughput capacity by 50% to
150,000 kg per year
Full Year 2018 Highlights
- Strengthened management team adding deep scientific,
processing, supply chain, finance and regulatory affairs
expertise
- Signed 4 multi-year tolling agreements with James E. Wagner
Cultivation Corporation, INDIVA Limited, Emerald Health
Therapeutics, Inc. and The Supreme Cannabis Company, Inc.
- Purchased 3.8 million grams of dried cannabis from multiple
Licensed Producers to build inventory of cannabis oil to address
significant consumer demand
- Initiated construction of MediPharm Labs Australia
state-of-the-art cannabis extraction facility with License expected
H2/19
- Completed equity financings of over $25 million and debuted as
a public company on the TSX Venture Exchange on October 4,
2018
- Awarded “Start-Up of the Year” at the Canadian Cannabis Awards
by Lift & Co
“2018 was a breakthrough year for MediPharm
Labs. We became the first fully Licensed Producer to specialize
solely in extraction and quickly scaled operations to emerge as the
dominant market leader in the manufacturing of high quality,
pharmaceutical-like production of cannabis derivative products –
the future of cannabis,” said Patrick McCutcheon, Chief Executive
Officer.
“As leading extraction specialists, we
demonstrated our ability to rapidly expand our footprint and
achieve significant revenue and positive operating cash flow just
weeks after receiving our sales License, and our strong operations
have continued into 2019. The strength of this performance
validates our uniquely focused strategy and investments. We are
proud that the MediPharm Labs team stands out among the top global
players in the cannabis industry producing tangible results with
significant future potential.”
2018 Key
Financial Measures |
|
|
|
Three months ended |
Year ended |
|
December 31, |
|
December 31, |
|
2018 |
|
2017 |
|
2018 |
|
2017 |
|
$(000’s) |
|
$(000’s) |
|
$(000’s) |
|
$(000’s) |
Revenues |
10,198 |
|
- |
|
10,198 |
|
- |
Gross profit |
3,967 |
|
- |
|
3,967 |
|
- |
Gross
margin % |
39% |
|
- |
|
39% |
|
- |
Net loss |
(3,542) |
|
(742) |
|
(8,466) |
|
(995) |
|
|
Adjusted EBITDA(1) |
2,129 |
|
(695) |
|
(875) |
|
(948) |
Adjusted
EBITDA(1) margin % |
21% |
|
- |
|
(9%) |
|
- |
|
|
2019 Year-to-Date Highlights
- Executed Private Label Sales Agreements in place valued in
excess of $85 million over 15-month period from December 2018
- Executed large Private Label cannabis oil sale for $35 million
with additional $13.5 million purchase option over 13-month
period
- Signed a 3-year Tolling Agreement with TerrAscend Corp.
- First extraction only LP to sign an International Private Label
Sale Agreement with AusCann Group Holdings Ltd. – Export of
cannabis oil from Canada to Australia for the manufacturing of
hard-shell cannabinoid capsules
- Launched White Label Solutions Platform to extract, purify,
formulate, process and distribute for LP’s, direct-to-consumer
brands and non-cannabis consumer packaged goods (CPG) companies for
provincial distribution
- Signed first White Label agreement to formulate, process and
distribute tincture bottles on behalf of an existing brand
commencing H2 2019
- Acquired over 5,000 KG of dried cannabis for Private Label
cannabis oil production in final two weeks of March
- Initiated trading on OTCQB under symbol “MLCPF” and FSE under
symbol “MLZ”
Mr. McCutcheon continued, “Looking ahead, we are now working on
an ambitious, well-planned agenda for 2019 that will enable
MediPharm Labs to extend our first-mover advantage. We are ramping
up production, adding capacity, targeting EU GMP certification,
expanding product offerings, developing R&D and IP, signing new
sales agreements, and executing on our M&A and international
growth pipeline.”
“Most importantly, we see all of this as a
starting point. We expect to accelerate our growth globally as the
size of our addressable market increases and we strengthen our
foothold domestically with the expected legalization of vapeables,
edibles, beverages and topicals providing a strong growth
trajectory in Canada. We will continue to capitalize on the
numerous opportunities available to us through effective capital
deployment and continued expert execution to create shareholder
value for the long term.”
2019 Strategic Priorities
- Forge additional domestic
and International sales and supply agreements – Utilizing
a first-mover and other proprietary advantages, the Company is
focused on procuring cost efficient, bulk dried cannabis supply,
increasing wholesale Private Label cannabis concentrate (crude
resin and distillate) production and value-added products, services
and tolling to win new business domestically and
internationally.
- Expand White-Label
Solutions Platform Including Formulation, Processing and
Distribution Services – Expected legalization of
vapeables, edibles, beverages and topicals in October 2019 is also
expected to expand the Company’s addressable market and act as a
catalyst to encourage a broad array of direct-to-consumer brands
and non-cannabis consumer packaged goods companies to seek partners
like MediPharm Labs for formulation, processing and provincial
distribution.
- Increase cGMP Production
Capacity – The Company is on track with the installation
and commissioning of 2 additional primary extraction lines at its
Barrie facility that are expected to increase annual processing
capacity to 250,000 kg over a total of 7 extraction lines.
Utilizing cGMP methodology, multiple extraction lines provide
flexibility to dedicate to specific customer batches and
significantly enhance productivity. Flexibility over multiple
extraction lines will be transformative, providing a continued
competitive advantage in the cannabis market.
- Achieve European Union GMP
Certification at Barrie Facility – Expect to achieve
certification in the H2 2019 enabling the Company to serve
substantial European demand.
- Complete First
International Facility in Australia – Australian centre of
excellence is expected to be commissioned in H2 2019, pending
licensing, and will act as hub to access Asia-Pacific regions.
The facility is designed to produce to cGMP standards with
annual extraction capacity of approximately 75,000 kg of dried
cannabis. The Australia region provides a strong backdrop for
cultivation given more favorable farming conditions where the
Company expects to procure locally sourced lower-cost supply inputs
for production.
- Expand Secondary Extraction
Capabilities – Advancing industrial-scale distillation and
commercial chromatography capabilities to produce active
pharmaceutical ingredients that require cannabinoid purity of at
least 99.9%. Development is underway for specialized,
proprietary chromatography processing with trials to commence H2
2019.
- M&A and Joint Venture
Opportunities – The Company has established a robust
pipeline of opportunities to replicate its unique business model in
other jurisdictions and complementary acquisitions to further
enhance and accelerate organic growth.
2018 Financial Highlights
All dollar amounts are expressed in Canadian
dollars unless otherwise stated.
|
Three months ended |
Year ended |
|
December 31, |
December 31, |
|
2018 |
|
2017 |
|
2018 |
|
2017 |
|
|
$(000’s) |
|
$(000’s) |
|
$(000’s) |
|
$(000’s) |
|
|
|
Revenue |
10,198 |
|
- |
|
10,198 |
|
- |
|
Cost of
sales |
(6,231 |
) |
- |
|
(6,231 |
) |
- |
|
|
|
Gross
profit |
3,967 |
|
- |
|
3,967 |
|
- |
|
|
|
|
|
|
|
|
|
|
General administrative
expenses |
(1,749 |
) |
(694 |
) |
(3,556 |
) |
(947 |
) |
Marketing and selling
expenses |
(597 |
) |
- |
|
(1,272 |
) |
- |
|
Share-based
compensation expense |
(738 |
) |
- |
|
(1,965 |
) |
- |
|
Transaction fee |
(4,230 |
) |
- |
|
(4,230 |
) |
- |
|
Other
operating expenses |
(19 |
) |
(1 |
) |
(996 |
) |
(1 |
) |
|
|
Operating
loss |
(3,366 |
) |
(695 |
) |
(8,052 |
) |
(948 |
) |
|
|
Finance income |
22 |
|
16 |
|
64 |
|
16 |
|
Finance
expense |
(198 |
) |
(63 |
) |
(478 |
) |
(63 |
) |
|
|
Net loss for the year |
(3,542 |
) |
(742 |
) |
(8,466 |
) |
(995 |
) |
|
|
|
|
Operating loss
– as reported |
(3,366 |
) |
(695 |
) |
(8,052 |
) |
(948 |
) |
|
|
Add: |
|
Share-based compensation expense |
738 |
|
- |
|
1,965 |
|
- |
|
Transaction fee |
4,230 |
|
- |
|
4,230 |
|
- |
|
Depreciation |
528 |
|
- |
|
982 |
|
- |
|
|
|
Adjusted
EBITDA(1) |
2,129 |
|
(695 |
) |
(875 |
) |
(948 |
) |
- Adjusted EBITDA is not a recognized
performance measure under IFRS, does not have a standardized
meaning and therefore may not be comparable to similar measures
presented by other issuers. Adjusted EBITDA is included as a
supplemental disclosure because Management believes that such
measurement provides a better assessment of the Company’s
operations on a continuing basis by eliminating certain non-cash
charges and charges or gains that are nonrecurring. Adjusted
EBITDA is defined as net loss excluding interest, taxes,
depreciation and amortization, and share-based compensation and
listing expense. Adjusted EBITDA has limitations as an analytical
tool as it does not include depreciation and amortization expense,
interest income and expense, taxes, share-based compensation and
transaction fees. 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. The most directly comparable measure to Adjusted EBITDA
calculated in accordance with IFRS is operating income (loss).
The above is a reconciliation of the Company’s operating loss
to Adjusted EBITDA. See “Reconciliation of non-IFRS measures” in
the Company’s Management’s Discussion and Analysis for the year
ended December 31, 2018 additional information.
About MediPharm Labs Corp.
Founded in 2015, MediPharm Labs has the
distinction of being the first company in Canada to become a
licensed producer for cannabis oil production under the ACMPR
without first receiving a cannabis cultivation license. This expert
focus on cannabis concentrates from our cGMP (current Good
Manufacturing Practices) and ISO standard clean rooms and critical
environments laboratory, allows MediPharm Labs to produce purified,
pharmaceutical-like cannabis oil and concentrates for advanced
derivative products. MediPharm Labs has invested in an expert,
research-driven team, state-of-the-art technology, downstream
extraction methodologies and purpose-built facilities to deliver
pure, safe and precisely-dosed cannabis products to patients and
consumers. MediPharm Labs’ private label program is a high margin
business for the Company, whereby it opportunistically procures dry
cannabis flower and trim from its numerous product supply partners,
to produce proprietary cannabis oil concentrate products for resale
globally on a private label basis.
Through its subsidiary, MediPharm Labs Australia
Pty. Ltd., MediPharm Labs has also completed its application
process with the federal Office of Drug Control to extract and
import medical cannabis products in Australia.
For further information, please
contact:Laura Lepore, Vice President, Investor
Relations & CommunicationsTelephone: 705-719-7425 ext
216Email: investors@medipharmlabs.com Website:
www.medipharmlabs.com
NEITHER THE TSX VENTURE EXCHANGE NOR ITS
REGULATION SERVICES PROVIDER (AS THAT TERM IS DEFINED IN THE
POLICIES OF THE TSXV) ACCEPTS RESPONSIBILITY FOR THE ADEQUACY OR
ACCURACY OF THIS RELEASE.
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, expectations for expanding product
offerings, development of R&D and IP, signing new sales and
supply agreements, expanding white-label solutions platform,
increasing production capacity, expanding merger and acquisition
and international growth pipeline, expanding secondary extraction
capabilities, GMP certification and the completion of Australian
facility and establishment of operations in Australia.
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 Labs to obtain
adequate financing; and the delay or failure to receive regulatory
approvals. 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 Labs assumes no
obligation to update the forward-looking statements of beliefs,
opinions, projections, or other factors, should they change.
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