– Record Q4, and F2021 Manufacturing Segment
Revenue of $5.3M, a 3-fold Increase vs. F2020 – Expansion of
Pliaglis® Licenses to 32 New Countries – Strong Liquidity Position
of $11.3M – Q4-F2021 Adjusted EBITDA1 of $1.6M
Crescita Therapeutics Inc. (TSX: CTX and OTC US: CRRTF)
(“Crescita” or the “Company”), a growth-oriented, innovation-driven
Canadian commercial dermatology company, today reported its
financial results for the three months and fiscal year ended
December 31, 2021 (“Q4-F2021” and “F2021”). All amounts presented
are in thousands of Canadian dollars (“CAD”) unless otherwise
noted.
Financial Highlights
Q4-F2021 vs. Q4-F2020
- Revenue was $7,562 compared to $2,791, up $4,771;
- Gross profit was $4,651 compared to $1,588, up $3,063;
- Operating expenses were $3,536 compared to $2,316, up
$1,220;
- Adjusted EBITDA1 was $1,585 compared to $(446), up $2,031;
F2021 vs. F2020
- Revenue was $16,769 compared to $15,640, up $1,129;
- Gross profit was $10,014 compared to $11,273, down $1,259;
- Operating expenses were $10,733 compared to $9,718, up
$1,015;
- Adjusted EBITDA1 was $932 compared to $3,201, down $2,269;
- Ending cash of $11,331 compared to $14,281, down $2,950.
“We made considerable headway in achieving near-term milestones
in 2021,” commented Serge Verreault, President and CEO of Crescita.
“Our business bounced back from the impacts of COVID-19 in the
prior year with 7.2% total revenue growth to $16.8 million. With a
strong balance sheet and encouraging consumer trends, we invested
in our commercial infrastructure this year. Our aim is to
accelerate product sales across all our channels, with a particular
emphasis on our digital footprint, and on expanding our presence in
the growing medical aesthetics market.
“We also added production volume to our plant, more than
tripling our revenue compared to 2020 and our manufacturing team is
streamlining our processes to enhance future scalability. We
expanded Pliaglis across the globe, adding three partners that will
commercialize Pliaglis in 32 new countries. With all major
countries now licensed, we are helping our partners obtain
regulatory approval to launch Pliaglis in 2022 and beyond so that
it becomes a solid recurring revenue stream for Crescita. With 2022
well underway, our team is stronger than ever and well positioned
to execute on our growth pillars,” concluded Mr. Verreault.
F2021 Corporate Developments
Expansion of our Board of Directors
- The Board of Directors appointed Mrs. Deborah Shannon-Trudeau
as a director effective November 10, 2021. Mrs. Trudeau has over 30
years’ experience in strategy, business development, commercial and
manufacturing operations.
Key New Partners for the Commercialization of Pliaglis in 32
Countries
- 8-Country Exclusive Licensing Agreement with Egis
Pharmaceuticals PLC, a pharmaceutical company in Central Eastern
Europe for the rights to Pliaglis.
- 15-Country Exclusive Licensing Agreement with STADA MENA
DWC-LLC, a subsidiary of STADA Arzneimittel AG, a specialty pharma,
generics and consumer healthcare group, for the rights to Pliaglis
in 15 countries in the Middle East and North Africa (“MENA”)
region.
- 9-Country Exclusive Licensing Agreement with Croma Pharma GmbH,
a globally acclaimed pharmaceutical company with specializations in
medical aesthetics, ophthalmology, and orthopaedics for the rights
to Pliaglis in eight European countries and Brazil.
Distribution Agreement with Obagi Cosmeceuticals LLC
- We entered into a distribution agreement with Obagi
Cosmeceuticals LLC (“Obagi”) providing us with the exclusive rights
to promote, distribute and sell the Obagi Medical® product line in
Canada. We expect to launch the Obagi line nationwide through our
existing sales network in the first half of 2022.
Acquisition of Minority Interest in The Best You®
- We acquired a minority interest in Akyucorp Ltd. d/b/a The Best
You, a privately held network of six medical aesthetic clinics in
Ontario (“The Best You”). In consideration, Crescita issued 470,128
common shares at a price of $0.70 per common share and to support
The Best You’s growth, we also invested in a secured convertible
promissory note with an initial principal amount of $0.5M that
could reach $1.25M based on financial performance and certain
events and conditions being met.
Launch of NCTF®
- We launched New Cellular Treatment Factor® (“NCTF”), a skin
revitalization solution primarily used for the improvement of skin
quality and fine lines. NCTF represents a key opportunity for us to
take advantage of the increasing popularity of minimally invasive
and non-invasive aesthetic procedures and to strengthen our
presence in the rapidly growing Canadian medical aesthetics
market.
Expansion of Production Volumes
- We received firm purchase orders of approximately $7 million in
our Manufacturing and Services segment, representing a significant
increase in production and sales volume. The increase is a result
of our customers’ anticipated launches into new key markets and may
not be representative of future orders.
Amendment to Credit Facility
- We amended our existing revolving demand operating credit
facility for a temporary $2.5 million increase in the available
amount from $3.5 million to $6.0 million until April 30, 2022. The
temporary increase provides us with additional financial
flexibility to fund increases in production volumes in the
Manufacturing and Services segment. The Company has not drawn down
any amounts from this facility.
Q4-F2021 and F2021 Financial Results
Note: The Management’s Discussion and Analysis
(“MD&A”), the consolidated audited Financial Statements and
accompanying notes for the fiscal year ended December 31, 2021 are
available at www.crescitatherapeutics.com/investors and have been
filed with SEDAR at www.sedar.com.
Summary Financial Results
In thousands of CAD, except per share data
and number of shares
Three months ended December
31,
Year ended December
31,
2021
2020
2021
2020
$
$
$
$
Commercial Skincare
2,270
2,079
7,469
6,704
Licensing and Royalties
2,367
359
3,967
7,224
Manufacturing and Services
2,925
353
5,333
1,712
Revenues
7,562
2,791
16,769
15,640
Cost of goods sold
2,911
1,203
6,755
4,367
Gross profit
4,651
1,588
10,014
11,273
Gross margin (%)
61.5%
56.9%
59.7%
72.1%
Research and development
171
325
634
1,101
Selling, general and administrative
3,018
1,743
8,720
7,126
Depreciation and amortization
347
248
1,379
1,491
Total operating expenses
3,536
2,316
10,733
9,718
Operating profit (loss)
1,115
(728)
(719)
1,555
Total other (income) expenses
84
(40)
298
1,035
Share of profit in associate
8
-
8
-
Income (loss) before income
taxes
1,039
(688)
(1,009)
520
Deferred income tax (recovery) expense
96
(96)
96
483
Net income (loss)
943
(592)
(1,105)
37
Adjusted EBITDA1
1,585
(446)
932
3,201
Earnings per share
Basic
$
0.04
$
(0.03)
$
(0.05)
$
-
Diluted
$
0.04
$
(0.03)
$
(0.05)
$
-
Weighted average number of common
shares outstanding
Basic
21,016,282
20,648,448
20,755,290
20,661,477
Diluted
22,295,112
20,648,448
20,755,290
20,969,205
Selected Balance Sheet
Information
Cash and cash equivalents, end of
period
11,331
14,281
Selected Cash Flow Information
Cash provided by (used in) operating
activities
(469)
568
(1,597)
5,608
Cash used in investing activities
(222)
-
(846)
(59)
Cash used in financing activities
(194)
(94)
(500)
(476)
Revenue We have three reportable segments: 1) Commercial
Skincare (“Commercial”), which manufactures and sells branded
non-prescription skincare products in both the Canadian and
international markets, and also commercializes Pliaglis and NCTF in
Canada; 2) Licensing and Royalties (“Licensing”), which primarily
generates revenue from licensing our intellectual property related
to Pliaglis or our transdermal delivery technologies; and 3)
Manufacturing and Services (“Manufacturing”), which generates
revenue from contract manufacturing and product development
services.
For the three months ended December 31, 2021, total revenue was
$7,562 compared to $2,791 for the three months ended December 31,
2020, representing an increase of $4,771. Our Licensing segment
revenue increased by $2,008 reflecting the recognition of minimum
guaranteed royalties of $1,279 (US$1,000) under our agreement with
Taro Pharmaceuticals Inc. (“Taro” and the “Taro Agreement”) and an
upfront payment of $932 (€650) in connection with the licensing
agreement with Egis, while our Manufacturing segment revenue
increased by $2,572, reflecting the additional purchase orders from
new and existing clients, combined with the recovery from the
impact of COVID-19 on our Manufacturing segment in the prior year.
Our Commercial Skincare segment posted an increase of $191, driven
by incremental sales of NCTF launched in 2021 and an increase in
domestic sales from our lead aesthetic brand, Laboratoire Dr
Renaud®, partly offset by lower export revenue in Asian
markets.
For the year ended December 31, 2021, total revenue was $16,769
compared to $15,640 for the year ended December 31, 2020,
representing an increase of $1,129. The most significant increases
came from our Manufacturing segment in the amount of $3,621,
reflecting purchase orders from new and existing clients, and from
our Commercial segment in the amount of $765, reflecting higher
product sales mainly driven by digital marketing investments and
the launch of NCTF, with both segments showing recovery from the
prior year’s COVID-19 impact. These increases were partly offset by
the $3,257 decrease in our Licensing segment, mainly as a result of
the one-time revenue recognized in the prior year from amending our
U.S. licensing agreement with Taro (the “Taro Amendment”) in the
amount of $4,483, offset in part by the minimum royalties under the
Taro Agreement and upfront payments under various Pliaglis
licensing agreements in the rest-of-world. No royalties were
recognized from the U.S. sales of Pliaglis during the year.
Gross Profit For the three months ended December 31,
2021, gross profit was $4,651, representing a gross margin of
61.5%, compared to $1,588 and 56.9%, respectively, for the three
months ended December 31, 2020. The increase of $3,063 in gross
profit and 4.6% in gross margin were both mainly due to the
increase in high-margin licensing revenue year-over-year as well
as, to a lesser extent, the benefit of higher manufacturing
volumes.
For the year ended December 31, 2021, gross profit was $10,014,
representing a gross margin of 59.7%, compared to $11,273 and
72.1%, respectively, for the year ended December 31, 2020. The
decrease in gross profit of $1,259 was mainly due to the drop in
high-margin licensing revenue year-over-year, partly offset by the
growth in our Commercial and Manufacturing segments and the benefit
of government wage and rent subsidies related to COVID-19. The
decrease in gross margin of 12.4% was mainly driven by the decrease
in high-margin licensing revenue and the unfavourable revenue mix
with higher Manufacturing segment revenue year-over-year, offset in
part by the benefit of higher manufacturing volumes.
Operating Expenses For the three months ended December
31, 2021, total operating expenses were $3,536 compared to $2,316
for the three months ended December 31, 2020, representing a net
increase of $1,220. The increase was primarily driven by higher
selling, general and administrative (“SG&A”) expenses, mainly
reflecting investments in advertising and promotion to grow our
brands and in various key positions across the organization, and to
a lesser extent, higher depreciation and amortization expense of
$99. These additional costs were partly offset by lower research
and development (“R&D”) spend of $154.
For the year ended December 31, 2021, total operating expenses
were $10,733 compared to $9,718 for the year ended December 31,
2020, representing a net increase of $1,015. The increase was
mainly reflective of a return to a pre-pandemic level of
headcount-related costs, investments in advertising and promotion
spend to grow our brands and in various key positions across the
organization, mainly in the sales, marketing and digital marketing
departments. These additional costs were partly offset by lower
R&D spend of $467, primarily reflecting the Company’s
proportionate funding of clinical development activities related to
CTX-101 in Q2-F2020, and to a lesser extent, lower depreciation
expense of $112.
During the year ended December 31, 2021, we recognized the
benefit of $777 in wage subsidies under the Canada Emergency Wage
Subsidy (“CEWS”) program, compared to $722 for the year ended
December 31, 2020. In Q2-F2020, we initiated cash conservation
measures including temporary layoffs and salary reductions in
response to the pandemic.
Cash and Cash Equivalents Cash and cash equivalents were
$11,331 at December 31 2021, reflecting a net year-over-year change
of $(2,950), mainly due to the cash used in operations, which
includes the impact of non-cash working capital items that will be
collected in the first half of fiscal 2022, the investment in a
secured convertible promissory note in connection with our minority
interest in The Best You, purchases of capital assets and
repurchase of shares under our Normal Course Issuer Bid.
Non-IFRS Financial Measures We report our financial
results in accordance with International Financial Reporting
Standards (“IFRS”). However, we use certain non-IFRS financial
measures to assess our Company’s performance. We believe these to
be useful to management, investors, and other financial
stakeholders in assessing Crescita’s performance. The non-IFRS
measures used in this press release do not have any standardized
meaning prescribed by IFRS and are therefore not comparable to
similar measures presented by other issuers. These measures should
be considered as supplemental in nature and not as a substitute for
the related financial information prepared in accordance with IFRS.
The following are the Company’s non-IFRS measures along with their
respective definitions:
- EBITDA is defined as earnings before interest, income taxes,
depreciation, and amortization.
- Adjusted EBITDA is defined as earnings before interest, income
taxes, depreciation and amortization, share of (profit) losses of
associates, other (income) expenses, share-based compensation
costs, goodwill and intangible asset impairment, and foreign
exchange (gains) losses, as applicable.
Management believes that Adjusted EBITDA is an important measure
of operating performance and cash flow and provides useful
information to investors as it highlights trends in the underlying
business that may not otherwise be apparent when relying solely on
IFRS measures. Below is a reconciliation of EBITDA and Adjusted
EBITDA to their closest IFRS measures.
In thousands of CAD dollars
Three months ended December
31,
Year ended December
31,
2021
2020
2021
2020
$
$
$
$
Net income (loss)
943
(592)
(1,105)
37
Adjust for:
Depreciation and amortization
347
248
1,379
1,491
Interest (income) expense, net
14
(29)
54
(39)
Deferred income tax (recovery) expense
96
(96)
96
483
EBITDA
1,400
(469)
424
1,972
Adjust for:
Share of profit in an associate
(8)
-
(8)
-
Share-based compensation
123
34
272
155
Foreign exchange (gain) loss
70
(11)
244
(176)
Impairment of intangible assets
-
-
-
1,918
Taro Amendment
-
-
-
(668)
Adjusted EBITDA
1,585
(446)
932
3,201
Caution Concerning Limitations of Summary Financial Results
Press Release This summary earnings press release contains
limited information meant to assist the reader in assessing
Crescita’s performance, but it is not a suitable source of
information for readers who are unfamiliar with Crescita and is not
in any way a substitute for the Company's Consolidated Audited
Financial Statements and notes thereto, MD&A and our latest
Annual Information Form (“AIF”).
About Crescita Therapeutics Inc. Crescita (TSX: CTX and
OTC US: CRRTF) is a growth-oriented, innovation-driven Canadian
commercial dermatology company with in-house R&D and
manufacturing capabilities. The Company offers a portfolio of
high-quality, science-based non-prescription skincare products and
early to commercial stage prescription products. We also own
multiple proprietary transdermal delivery platforms that support
the development of patented formulations to facilitate the delivery
of active ingredients into or through the skin. For more
information visit, www.crescitatherapeutics.com.
Forward-looking Statements This press release contains
“forward-looking information” within the meaning of applicable
securities laws (collectively, “forward-looking statements”).
Forward-looking statements can be identified by words such as:
“anticipate”, “intend”, “plan”, “goal”, “seek”, “believe”,
“project”, “estimate”, “expect”, “strategy”, “future”, “likely”,
“may”, “should”, “will” and similar references to future periods.
Examples of forward-looking statements include, but are not limited
to, statements regarding the Company’s objectives, plans, goals,
strategies, growth, performance, operating results, strategy for
customer retention, product development, market position, business
prospects, opportunities and industry trends and similar statements
concerning anticipated future events, results, circumstances,
performance or expectations. Forward-looking statements are neither
historical facts nor assurances of future performance. Instead,
they are based only on current beliefs, expectations and
assumptions regarding the future of the Company’s business, future
plans and strategies, projections, anticipated events and trends,
the economy and other future conditions. Because forward-looking
statements relate to the future, they are subject to inherent
uncertainties, risks and changes in circumstances that are
difficult to predict and many of which are outside of the Company’s
control. Crescita’s actual results and financial condition may
differ materially from those indicated in the forward-looking
statements. Therefore, you should not unduly rely on any of these
forward-looking statements. Important factors that could cause
Crescita’s actual results and financial condition to differ
materially from those indicated in the forward-looking statements
include, among others: economic and market conditions, the impact
of the COVID-19 pandemic and the response thereto of governments
and consumers, the Company’s ability to execute its growth
strategies, reliance on third parties for clinical trials,
marketing, distribution and commercialization, the impact of
changing conditions in the regulatory environment and product
development processes, manufacturing and supply risks, increasing
competition in the industries in which the Company operates, the
Company’s ability to meet its debt commitments, the impact of
unexpected product liability matters, the impact of litigation
involving the Company and/or its products, the impact of changes in
relationships with customers and suppliers, the degree of
intellectual property protection of the Company’s products, the
degree of market acceptance of the Company’s products, developments
and changes in applicable laws and regulations, as well as other
risk factors discussed in the “Risk Factors” sections of the
Company’s most recent annual MD&A for the year ended December
31, 2021 and the Company’s AIF dated March 22, 2022. Any
forward-looking statement made in this press release is based only
on information currently available and speaks only as of the date
on which it is made. Except as required by applicable securities
laws, Crescita undertakes no obligation to publicly update any
forward-looking statement, whether written or oral, that may be
made from time to time, whether as a result of new information,
future developments or otherwise.
______________________ 1Please refer to the Non-IFRS Financial
Measures section of this press release.
View source
version on businesswire.com: https://www.businesswire.com/news/home/20220323005350/en/
Crescita Therapeutics Investor Relations Linda Kisa, CPA,
CA lkisa@crescitatx.com
Crescita Therapeutics (TSX:CTX)
過去 株価チャート
から 10 2024 まで 11 2024
Crescita Therapeutics (TSX:CTX)
過去 株価チャート
から 11 2023 まで 11 2024