Strong Ending Cash Balance of $9.3M
LAVAL, QC, Aug. 12, 2020 /CNW Telbec/ - Crescita
Therapeutics Inc. (TSX: CTX) (OTC US: CRRTF) ("Crescita" or
the "Company"), a growth-oriented, innovation-driven Canadian
commercial dermatology company with in-house research &
development ("R&D") and manufacturing capabilities, today
reported its financial results for the second quarter ended
June 30, 2020 ("Q2-F2020").
All amounts in this press release are in thousands of
Canadian dollars ("CAD") unless otherwise noted.
Financial Highlights - Q2-F2020 vs.
Q2-F2019
- Revenue was $1,733, a decrease of
$7,629. In Q2-F2019, the Company
recognized $5,459 in up-front
payments and guaranteed future minimum royalties in connection with
the out-licensing agreement with Cantabria Labs ("Cantabria" and
the "Cantabria Agreement");
- Gross profit was $1,092,
representing a gross margin of 63.0%;
- Operating expenses (excluding COGS) were $2,318, a decrease of $1,012;
- Recorded a non-cash impairment charge on intangible assets of
$1,918 to reflect the projected
impact of the pandemic-driven decrease in demand for certain
products and services;
- Adjusted EBITDA1 was $(781), a decrease of $5,864, mainly due to the revenue recognized in
connection with the Cantabria Agreement in Q2-F2019 of $5,459;
- Ending cash position was $9,265,
a decrease of $69 versus Q1-F2020 and
flat versus Q4-F2019.
"While our Q2 results were affected by the COVID-19 pandemic, we
are confident that the financial and operational measures we have
taken ensure that Crescita is well positioned to participate in the
industry recovery," said Serge
Verreault, President and CEO. "Our strong liquidity position
at the end of the quarter despite the pandemic, will be
further enhanced by the approximately CAD$5.2 million to be received under the Taro
contract amendment, and will allow us to continue investing
strategically to grow our revenue streams and pursue business
development opportunities."
Q2-F2020 Corporate Developments
- On June 24, 2020, Crescita's
licensing partner, Cantabria Labs received approval from European
regulatory authorities for its manufacturing facility in
Santander Spain to be the supplier
of Pliaglis® in Europe.
In connection with the approval, the Company revised its estimate
of the present value of future guaranteed minimum royalties to be
received over the term of the contract, recognizing $413 in the quarter.
- On May 11, 2020, the Company
started progressively re-opening its manufacturing and office
facility following authorization from the Québec provincial
government. The facility is now fully operational and the majority
of the employees that were temporarily laid off have been rehired
and restored to a five-day work week. In addition, executive
salaries and board of directors fees, which had been temporarily
reduced in response to the pandemic, were restored as of
July 1, 2020.
Subsequent Event
- On July 28, 2020, the Company
announced that it entered into an amendment to the development and
commercialization agreement with Taro Pharmaceuticals Inc. ("Taro")
with regard to Pliaglis® in the United States. The amendment entitles the
Company to receive a one-time payment of US$3,900 (approximately CAD$5,200), largely representing a royalty
adjustment to past sales as well as an upward modification of
future royalty payments.
1Please
refer to the Non-IFRS Financial Measures and EBITDA and Adjusted
EBITDA Reconciliation sections of this press
release.
|
Q2-F2020 Financial Results
Note: The Management's Discussion and
Analysis ("MD&A"), Condensed Consolidated Interim Financial
Statements and accompanying notes for the three and six months
ended June 30, 2020 can be found at
www.crescitatherapeutics.com/investors and have been filed with
SEDAR at www.sedar.com.
Summary Financial
Results
|
|
In thousands of
CAD except earnings per share and number of shares
|
|
Three months ended
June 30,
|
|
|
Six months ended
June 30,
|
|
2020
|
|
2019
|
|
|
2020
|
|
2019
|
|
|
$
|
|
$
|
|
|
$
|
|
$
|
Revenues
|
|
1,733
|
|
9,362
|
|
|
5,548
|
|
13,611
|
Cost of goods
sold
|
|
641
|
|
1,423
|
|
|
1,992
|
|
2,650
|
Gross
Profit
|
|
1,092
|
|
7,939
|
|
|
3,556
|
|
10,961
|
Gross margin as a
% of revenue
|
|
63.0%
|
|
84.8%
|
|
|
64.1%
|
|
80.5%
|
|
|
|
|
|
|
|
|
|
|
Research &
development
|
|
336
|
|
609
|
|
|
564
|
|
876
|
Selling, general
& administrative
|
|
1,568
|
|
2,311
|
|
|
3,751
|
|
4,243
|
Depreciation and
Amortization
|
|
414
|
|
410
|
|
|
828
|
|
766
|
Total operating
expenses (excl. COGS)
|
|
2,318
|
|
3,330
|
|
|
5,143
|
|
5,885
|
Operating profit
(loss)
|
|
(1,226)
|
|
4,609
|
|
|
(1,587)
|
|
5,076
|
Total other
expenses
|
|
1,859
|
|
1,322
|
|
|
1,812
|
|
1,511
|
Income (loss)
before income taxes
|
|
(3,085)
|
|
3,287
|
|
|
(3,399)
|
|
3,565
|
Deferred income tax
expense
|
|
-
|
|
1,079
|
|
|
180
|
|
1,315
|
Net income
(loss)
|
|
(3,085)
|
|
2,208
|
|
|
(3,579)
|
|
2,250
|
Net income (loss)
per share
|
|
|
|
|
|
|
|
|
|
- Basic
|
$
|
(0.15)
|
$
|
0.11
|
|
$
|
(0.17)
|
$
|
0.11
|
- Diluted
|
$
|
(0.15)
|
$
|
0.10
|
|
$
|
(0.17)
|
$
|
0.10
|
Weighted average
number of common shares
|
|
|
|
|
|
|
|
|
|
- Basic
|
|
20,648,448
|
|
21,016,059
|
|
|
20,674,433
|
|
21,016,059
|
- Diluted
|
|
21,856,142
|
|
22,486,406
|
|
|
22,065,724
|
|
22,305,542
|
Selected Balance
Sheet Information
|
|
|
|
|
|
|
|
|
|
Cash and cash
equivalents, end of period
|
|
9,265
|
|
11,689
|
|
|
9,265
|
|
11,689
|
Long-term
debt
|
|
-
|
|
3,558
|
|
|
-
|
|
3,558
|
Selected Cash Flow
Information
|
|
|
|
|
|
|
|
|
|
Cash provided by
(used in) operating activities
|
|
84
|
|
1,224
|
|
|
350
|
|
3,622
|
Cash used in
investing activities
|
|
(37)
|
|
(80)
|
|
|
(61)
|
|
(114)
|
Cash used in
financing activities
|
|
(89)
|
|
(328)
|
|
|
(292)
|
|
(403)
|
Revenue
The Company generates revenue from its three
reportable segments: 1) Commercial Skincare ("Commercial"), which
manufactures branded non-prescription skincare products for sale in
both the Canadian and international markets; 2) Licensing and
Royalties ("Licensing"), which includes revenue from the licensing
of intellectual property related to Pliaglis or for the use of its
transdermal delivery technologies; and 3) Manufacturing and
Services ("Manufacturing"), which includes revenue from contract
manufacturing and product development services ("CDMO") offered to
our clients.
For the three months ended June 30,
2020, total revenue was $1,733
compared to $9,362 for the three
months ended June 30, 2019,
representing a year-over-year decrease of $7,629. Revenues decreased across all three
segments, with the largest decrease in the Licensing segment,
representing $6,284 year-over-year.
In Q2-F2019, the Company recognized a total of $5,459 in connection with the Cantabria
Agreement, made up of $3,721 in
up-front payments and $1,738 in
future guaranteed minimum royalties, while in Q2-F2020, the Company
recorded $413 in future guaranteed
minimum royalties under the agreement. The Commercial and
Manufacturing segments posted decreases of $663 and $682,
respectively, mainly due to lower product demand driven by
COVID-19-related shutdowns of personal services businesses such as
spas and medispas, throughout most of the second quarter.
For the six months ended June 30,
2020, total revenue was $5,548
compared to $13,611 in the comparable
six-month period of 2019. The decrease of $8,063 across all our segments was primarily a
result of the same factors as discussed for the quarter.
Cost of Goods Sold ("COGS") and Gross Profit
For the
three and six months ended June 30,
2020, total COGS were $641 and
$1,992, respectively, compared to
$1,423 and $2,650 for the three and six months ended
June 30, 2019, representing decreases
of $782 and $658, respectively. The year-over-year decreases
were primarily due to lower revenue across all three segments,
mainly as a result of COVID-19 related business and product demand
disruptions, as explained previously, as well as the timing and mix
of CDMO sales in our Manufacturing segment, partly offset by the
lower cost of earning royalties on the net sales of Pliaglis in the
Licensing segment versus the prior year periods.
For the three and six months ended June
30, 2020, gross profit was $1,092 and $3,556,
representing a gross margin of 63.0% and 64.1%, respectively,
compared to $7,939 or 84.8% and
$10,961 or 80.5%, respectively, for
the comparable three and six-month periods of 2019. The decreases
in gross profit and gross margin for both periods were mainly due
to: lower revenue across all three segments, as described
previously, and specifically from the aggregate full margin revenue
of $5,459 recognized under the
Cantabria Agreement in Q2-F2019 which did not repeat, as
well as the impact of our product mix and unfavourable
manufacturing variances.
Operating Expenses (excluding COGS)
For the three
months ended June 30, 2020, total
operating expenses were $2,318,
compared to $3,330 for the three
months ended June 30, 2019,
representing a year-over-year decrease of $1,012. The year-over-year decrease was mainly
driven by lower selling, general and administrative ("SG&A")
and R&D expenses of $743 and
$273, respectively. The Q2-F2020
results reflect the full quarter's impact of cost savings from the
cash conservation measures implemented by the Company in response
to the COVID-19 pandemic.
For the six months ended June 30,
2020, total operating expenses were $5,143, compared to $5,885 for the six months ended June 30, 2019, representing a net year-over-year
decrease of $742, mainly as a result
of the implementation of measures in response to COVID-19, partly
offset by higher depreciation and amortization expense in the first
half of 2020.
Impairment of Intangible Assets
For the three and six
months ended June 30, 2020, the
Company recognized an impairment charge of $1,918. The Company updated its impairment
assessment at June 30, 2020, mainly
to reflect the projected impact of the pandemic-driven decrease in
demand for its non-prescription skincare products and contract
manufacturing services on its long-term forecasts.
Income (Loss) before Income Taxes
For the three months
ended June 30, 2020, the Company
reported a loss before income taxes of $(3,085), compared to income of $3,287 reported for the three months ended
June 30, 2019. The year-over-year
decrease of $6,372 was mainly
attributable to: 1) the reduction in gross margin of $1,801 across all segments, as explained
previously, but excluding the impact of the Cantabria Agreement; 2)
the benefit of the upfront payment and future guaranteed minimum
royalties under the Cantabria Agreement of $3,772 in Q2-F2019, net of contract termination
fees; 3) the impairment charge of $1,918 taken in the quarter, partly offset by: 1)
a reduction in R&D expenses of $273; 2) a reduction in SG&A expenses of
$743; 3) a reduction in net interest
expense of $93 as a result of the
repayment in full of the Company's long-term debt with Knight
Therapeutics Inc. (the "Knight Loan") in Q4-F2019 and the interest
income accretion recognized on the contract asset related to the
Cantabria Agreement.
For the six months ended June 30,
2020, the Company reported a loss before income taxes of
$(3,399), compared to income of
$3,565 reported for the six months
ended June 30, 2019. The
year-over-year decrease of $6,964 was
mainly attributable to: 1) the reduction in gross margin of
$2,359 across all segments, as
explained previously, but excluding the impact of the Cantabria
Agreement; 2) the benefit of the upfront payment and future
guaranteed minimum royalties under the Cantabria Agreement of
$3,772, net of contract termination
fees recognized in Q2-F2019; 3) the impairment charge of
$1,918 taken in the quarter; partly
offset by 1) the decrease in SG&A costs of $492; 2) the decrease in R&D costs of
$312; 3) a reduction in net interest
expense of $214; and 4) the
favourable impact of foreign exchange gains year-over-year in the
amount of $129.
Cash and Cash Equivalents
Cash and cash equivalents
were $9,265 as at June 30, 2020 compared to $11,689 as at
June 30, 2019, representing a
year-over-year decrease of $2,424.
During the fourth quarter ended December 31,
2019, the Company repaid the outstanding balance of the
Knight Loan in the amount of $3,570.
Non-IFRS Financial Measures
The Company reports
its financial results in accordance with 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 from both a financial and operational standpoint. 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 (loss) before interest, income
taxes, depreciation, and amortization.
- Adjusted EBITDA is defined as earnings (loss) before interest,
income taxes, depreciation and amortization, gain on settlement,
other income, equity-settled stock-based compensation ("SBC"), gain
on debt renegotiations, goodwill and intangible assets impairment,
termination and other costs, and foreign currency 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. A reconciliation of EBITDA and adjusted EBITDA to
their closest IFRS measure can be found below.
In thousands of
CAD
|
Three months ended
June 30,
|
|
Six months ended
June 30,
|
2020
|
2019
|
|
2020
|
2019
|
|
$
|
$
|
|
$
|
$
|
Net income
(loss)
|
(3,085)
|
2,208
|
|
(3,579)
|
2,250
|
Add:
|
|
|
|
|
|
Depreciation and
amortization
|
414
|
410
|
|
828
|
766
|
Interest expense,
net
|
(8)
|
85
|
|
(5)
|
209
|
Deferred income tax
expense
|
-
|
1,079
|
|
180
|
1,315
|
EBITDA
|
(2,679)
|
3,782
|
|
(2,576)
|
4,540
|
Equity-settled
stock-based compensation
|
31
|
64
|
|
90
|
197
|
Foreign currency
loss
|
-
|
-
|
|
-
|
28
|
Intangible asset
impairment
|
1,918
|
-
|
|
1,918
|
-
|
Termination fees and
other costs
|
-
|
1,274
|
|
-
|
1,274
|
Less:
|
|
|
|
|
|
Foreign exchange
gain
|
51
|
37
|
|
101
|
-
|
Adjusted
EBITDA
|
(781)
|
5,083
|
|
(669)
|
6,039
|
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 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 non-prescription
skincare products and early to commercial stage prescription drug
products and owns multiple proprietary drug delivery platforms that
support the development of patented formulations that can
facilitate the delivery of active ingredients into or through the
skin.
Supported by a sales force covering Canada and executing a business to business to
consumer marketing approach, Crescita sells its non-prescription
skincare products domestically through spas, medispas, and medical
aesthetic clinics, as well as internationally, through
distributors.
Crescita's portfolio also includes a prescription product called
Pliaglis®, that utilizes the Company's proprietary
phase-changing topical cream Peel technology, a part of the
DuraPeel™ family, which are self-occluding, film-forming cream/gel
formulations, that provide extended release delivery of the active
ingredients to the site of application. Pliaglis is a topical local
anesthetic cream that provides safe and effective local dermal
analgesia on intact skin prior to superficial dermatological
procedures. The product is currently approved in over 25 different
countries and sold by commercial partners in the U.S., Italy, and Brazil, and sold in Canada by the Company.
Crescita's expertise in product formulation and development can
be leveraged in combination with its patented transdermal delivery
technologies to develop and manufacture creams, liquids, gels,
ointments and serums under its CDMO infrastructure. The Company
operates out of a 50,000 square-foot facility located in
Laval, Québec, which produces the
majority of its non-prescription skincare products, such as LDR,
Pro-Derm, Dermazulene and Alyria. Formulations manufactured by or
for Crescita include cosmetics, natural health products and
products with Drug Identification Numbers. For additional
information, please visit www.crescitatherapeutics.com.
Forward-Looking Statements
This press release
contains "forward-looking information" as defined under Canadian
securities laws (collectively, "forward-looking statements"). The
words "plans", "expects", "does not expect", "goals", "seek",
"strategy", "future", "estimates", "intends", "anticipates", "does
not anticipate", "projected", "believes" or variations of such
words and phrases or statements to the effect that certain actions,
events or results "may", "will", "could", "would", "should",
"might", "likely", "occur", "be achieved" "continue" or "temporary"
and similar expressions identify forward-looking statements
and include statements regarding the Company's plans, objectives
and responses to the COVID-19 pandemic. In addition, any statements
that refer to expectations, intentions, projections or other
characterizations of future events or circumstances contain
forward-looking statements.
Forward-looking statements are not historical facts but instead
represent management's expectations, estimates, projections and
assumptions regarding future events or circumstances. Such
forward-looking statements are qualified in their entirety by the
inherent risks, uncertainties and changes in circumstances
surrounding future expectations which are difficult to predict and
many of which are beyond the control of the Company.
Forward-looking statements are necessarily based on a number of
estimates and assumptions that, while considered reasonable by
management of the Company as of the date of this press release, are
inherently subject to significant business, economic and
competitive uncertainties and contingencies. Material factors and
assumptions used to develop the forward-looking statements, and
material risk factors that could cause actual results to differ
materially from the forward-looking statements, include but are not
limited to the risks of, and future impacts related to, COVID-19,
including the response of domestic and international governments to
the virus; the impact of COVID-19 on the Company's operations,
personnel, supply chain, product sales, royalties, customer demand
and financial flexibility; changes in the business or affairs
of Crescita; the ability of Crescita's licensees to successfully
market its products; competitive factors in the industries in which
Crescita operates; relationships with customers, suppliers and
licensees; changes in legal and regulatory requirements; foreign
exchange and interest rates; prevailing economic conditions; and
other factors, many of which are beyond the control of
Crescita.
Additional 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, the risk
factors included in Crescita's most recent Annual Information Form
under the heading "Risks Factors", and as described from time to
time in the reports and disclosure documents filed by Crescita with
Canadian securities regulatory authorities and commissions. These
and other factors should be considered carefully, and readers
should not place undue reliance on Crescita's forward-looking
statements when making decisions, as forward-looking statements
involve significant risks and uncertainties. Forward-looking
statements should not be read as guarantees of future performance
or results and will not necessarily be accurate indications of
whether or not the times at or by which such performance or results
will be achieved.
All forward-looking statements are based only on information
currently available to the Company and are made as of the date of
this press release. Except as expressly required by applicable
Canadian securities law, the Company assumes no obligation to
publicly update or revise any forward-looking statement, whether as
a result of new information, future events or otherwise. All
forward-looking statements in this press release are qualified by
these cautionary statements.
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SOURCE Crescita Therapeutics Inc.