Acerus Pharmaceuticals Corporation (“Acerus” or the “Company”)
(TSX: ASP; OTCQB: ASPCF) today reported its financial results for
the three-month period ended March 31, 2021. Unless otherwise
noted, all amounts are in US dollars and are prepared in accordance
with International Financial Reporting Standards (“IFRS”).
Q1 - 2021 Highlights
- Re-purchased
all remaining NATESTO® rights from Aytu Biopharma, allowing Acerus
to build and leverage its commercial business across North
America
- Expanded
NATESTO® access to 20 countries across Europe, Central Asia and the
Middle East through an agreement with Maylen Farma (“Maylen”), a
firm based in Lugano, Switzerland that specializes in bringing
pharmaceutical products and healthcare services to patients in
emerging markets
- Received notice
of allowance on NATESTO® patent in the U.S. that will have an
expiry date in 2034, protecting one of the Company’s proprietary
medications into the foreseeable future
- Completed a
US$15 million subordinated secured loan facility (the “Loan
Facility”), providing needed capital to execute the Company’s many
ongoing growth initiatives
- After the end
of the quarter, Acerus announced a NATESTO® revenue share agreement
with Amneal Pharmaceuticals, leveraging Amneal’s extensive
relationships with Endocrinology healthcare providers in the
U.S.
“We accomplished a great deal strategically in
the first quarter, all of which should position us for higher
growth going forward,” said Ed Gudaitis, President and Chief
Executive Officer of Acerus. “Re-purchasing the remaining NATESTO®
rights from Aytu – while necessitating a US$7.5 million termination
fee paid over 30 months – allowed us to actively take control of
our sales efforts in the U.S. and, in doing so, report all revenue
from this very important market. Other decisions this quarter also
strengthened the Company’s outlook – including our agreement with
Maylen, bolstering our overseas expansion plans, and our entering
into a new loan facility that provides capital for growth. Just as
importantly, after the end of the quarter, our deal with Amneal
paves the way for Acerus to more rapidly reach Endocrinology
professionals in the U.S., opening up new avenues for customer
interaction and acceptance. As we look out on 2021 and beyond, we
believe these strategic moves provide the flexibility and
opportunity for improved performance and bottom-line results.”
Summary of Results for the Three Months
Ended March 31, 2021 (compared to the Three Months Ended March 31,
2020 unless otherwise noted)
- Total revenue
in the quarter was negative $6.0 million compared to $0.1 million
in the first quarter of 2020, reflecting a $6.2 million termination
fee in 2021 related to the Aytu buyback of product rights; this fee
represents the present value of $7.5 million in total payments to
be made to Aytu under the agreement. Going forward, Acerus gains
full distribution rights and the reporting of sales for any
transaction in the U.S.
- Gross profit in
the first quarter of 2021 was negative $6.2 million compared to
negative $0.1 million in the prior-year period, reflecting the
aforementioned termination fee of $6.2 million
- Research and
development ("R&D") expense rose by $0.4 million, to $1.0
million, for the current quarter from $0.6 million in the
prior-year period, reflecting increased expense for NATESTO®
clinical trials in the U.S.
- Selling,
general and administrative expenses (“SG&A”) increased by $1.7
million. to $5.3 million, from $3.6 million in the prior-year
period, reflecting investment in the Company’s U.S. organization,
launched in the second half of 2020
- EBITDA1 was a
loss of $12.1 million compared to a loss of $3.8 million in the
prior-year period; Adjusted EBITDA1 was a loss of $5.7 million for
the quarter compared to a loss of $4.0 million in the prior-year
period
- The Company
incurred a net loss of $12.8 million, or $(0.01) per share, for the
quarter compared to a loss of $4.7 million, or $(0.01) per share,
in the first quarter of 2020
Balance Sheet
Cash as of March 31, 2021 was $5.2 million
compared with $9.2 million as of December 31, 2020, reflecting cash
used during the quarter.
On April 30, 2021, the Company announced that it
had entered into a US$15 million subordinated secured loan facility
made available to the Company by way of one or more advances under
a secured grid promissory note with First Generation Capital Inc.,
a company affiliated with the Chairman of the Board of Directors of
Acerus.
COMPANY UPDATE AND OUTLOOK
NATESTO® The Company continues
to execute on its strategy of focusing on the U.S. market for
NATESTO®. During the quarter, the Company signed an agreement with
Aytu BioPharma (f/k/a Aytu BioScience) (“Aytu”), whereby Acerus
acquired all remaining rights to NATESTO® in the U.S. that were not
already returned as part of the Company’s 2019 Amended and Restated
Agreement with Aytu. By assuming full ownership of NATESTO and its
U.S. distribution, the Company can leverage its commercial business
unit to accelerate growth. In addition to Acerus selling to its
existing specialty healthcare professionals, the Company gains full
distribution rights and reporting of sales for any transaction in
the U.S. market. Aytu has agreed to assist Acerus throughout a
120-day transition period from the effective date (March 31, 2021)
and, during this period, will continue to provide distribution of
NATESTO® under the terms of the existing License and Supply
Agreement. NATESTO® sales will be recognized at the distributor
level, which allows for better alignment of revenue to underlying
prescription trends.
After the end of the quarter, in May 2021,
Acerus announced a NATESTO® co-promotion agreement with Amneal
Pharmaceuticals that leverages that company’s extensive
relationships with Endocrinology healthcare providers in the U.S.
market. Under the terms of the agreement, Amneal will sell NATESTO®
to its existing Endocrinology targets through June 30, 2024. In
compensation for such marketing efforts, Amneal will receive a
commission for most of the net profits attributed to Endocrinology
targets in the three active promotional years, with Acerus
retaining a low double-digit percentage of such net profits during
the active promotion period. Amneal will also receive a three-year
trailing royalty following the active promotion period, with
compensation to Amneal decreasing from a majority of the net
profits to a minority of the net profits.
Also subsequent to the end of the quarter, the
Company received a Notice of Allowance for a U.S. patent covering
NATESTO®. When granted, Acerus expects this patent to be listed in
the Orange Book, which will extend patent coverage through
2034.
Outside of the United States, the Maylen Farma
agreement announced in the quarter expands the reach of NATESTO® to
20 countries across Europe, Central Asia, and the Middle East.
Nations covered by the agreement include Belarus, Georgia, and
Ukraine; Azerbaijan, Uzbekistan, Tajikistan, Kazakhstan, and
Kyrgyzstan; Albania, Kosovo, North Macedonia, Serbia, and Bosnia
and Herzegovina; the United Arab Emirates, Kingdom of Saudi Arabia,
Kuwait, Qatar, Bahrain, Jordan, and Lebanon. The Company currently
expects first orders under his agreement in the second quarter,
with deliveries in the fourth quarter of 2021 and early 2022.
The Company also remains optimistic about a
return of NATESTO® to Canada during 2021. The first batch of
NATESTO® for this market has already been manufactured and is
undergoing stability studies. At the same time, Acerus has begun
the regulatory work and commercial preparations required to support
the reintroduction of NATESTO® in Canada.
avanafil Health Canada Approval
StatusThe review of the avanafil New Drug Submission
(“NDS”) is underway, and the Company is responding to questions and
clarification requests from Health Canada. As disclosed in the
Company’s 2020 fourth quarter earnings report, the review process
can take up to a year from receipt of the NDS (December 2020).
Conference Call Shareholders
are reminded that the conference call to discuss the Company’s
results for the first quarter will be held on May 13, 2021 at 10:00
a.m. Eastern Time.
To access the call live, please dial
416-406-0743 or 1-800-952-5114 and use access code 1930457#.
Listeners are encouraged to dial in 10 minutes before the call
begins to avoid delays. A replay of the conference call will be
available until 10:00 a.m. Eastern Time on Thursday, May 20, 2021
by dialing 905-694-9451 or 1-800-408-3053, using access code:
8998151#.
About Acerus Acerus
Pharmaceuticals Corporation is a Canadian-based specialty
pharmaceutical company focused on the commercialization and
development of innovative prescription products that improve
patient experience, with a primary focus in the field of men’s
health. The Company commercializes its products via its own
salesforce in the United States and Canada, and through a global
network of licensed distributors in other territories. Acerus’
shares trade on TSX under the symbol ASP and on OTCQB under the
symbol ASPCF. For more information, visit www.aceruspharma.com and
follow us on Twitter and LinkedIn.
1 Non-IFRS Financial
Measures - EBITDA and Adjusted EBITDAThe
non-IFRS measures included in this press release are not recognized
measures under IFRS and do not have a standardized meaning
prescribed by IFRS and may not be comparable to similar measures
presented by other issuers. When used, these measures are defined
in such terms as to allow the reconciliation to the closest IFRS
measure. These measures are provided as additional information to
complement those IFRS measures by providing further understanding
of our results of operations from our perspective. Accordingly,
they should not be considered in isolation nor as a substitute for
analysis of our financial information reported under IFRS. Despite
the importance of these measures to management in goal setting and
performance measurement, we stress that these are non-IFRS measures
that may have limits in their usefulness to investors.
We use non-IFRS measures, such as EBITDA and
Adjusted EBITDA to provide investors with a supplemental measure of
our operating performance and thus highlight trends in our core
business that may not otherwise be apparent when relying solely on
IFRS financial measures. We also believe that securities analysts,
investors and other interested parties frequently use non-IFRS
measures in the valuation of issuers. We also use non-IFRS measures
in order to facilitate operating performance comparisons from
period to period, prepare annual operating budgets, and to assess
our ability to meet our future debt service, capital expenditure
and working capital requirements.
The definition and reconciliation of EBITDA and
Adjusted EBITDA used and presented by the Company to the most
directly comparable IFRS measures follows below:
EBITDA is defined as net (loss)/income adjusted
for income tax, depreciation of property and equipment,
amortization of intangible assets, interest on long-term debt and
other financing costs, interest income, licensing revenue and
changes in fair values of derivative financial instruments.
Management uses EBITDA to assess the Company’s operating
performance.
Adjusted EBITDA is defined as EBITDA adjusted
for, as applicable, royalty expenses associated with triggering
events, milestones, share based compensation, impairment of
intangible asset, foreign exchange (gain)/loss, charges related to
product recall and gain on extinguishment of payables. We use
Adjusted EBITDA as a key metric in assessing our business
performance when we compare results to budgets, forecasts and prior
years. Management believes Adjusted EBITDA is an alternative
measure of cash flow generation than, for example, cash flow from
operations, particularly because it removes cash flow fluctuations
caused by extraordinary changes in working capital. A
reconciliation of net (loss)/income to EBITDA (and Adjusted EBITDA)
is set out below.
|
|
|
For the three months
ended March 31, |
|
|
|
|
2021 |
|
|
2020 |
|
Net
loss |
|
|
$ |
(12,826 |
) |
$ |
(4,663 |
) |
Adjustments: |
|
|
|
|
Amortization
of intangible assets |
|
|
37 |
|
|
179 |
|
|
Depreciation
of property and equipment |
|
|
222 |
|
|
64 |
|
|
Depreciation
of right of use asset |
|
|
- |
|
|
12 |
|
|
Interest
expense and other financing costs |
|
|
292 |
|
|
846 |
|
|
Interest
income |
|
|
(5 |
) |
|
(31 |
) |
|
Change in
fair value of derivative |
|
|
69 |
|
|
(163 |
) |
|
Loss on
modification of debt |
|
|
64 |
|
|
- |
|
EBITDA |
|
|
$ |
(12,147 |
) |
$ |
(3,756 |
) |
|
|
|
|
|
Termination Fee |
|
|
6,204 |
|
|
- |
|
Share based compensation |
|
|
291 |
|
|
45 |
|
Foreign exchange gain |
|
|
(15 |
) |
|
(244 |
) |
Adjusted EBITDA |
|
$ |
(5,667 |
) |
$ |
(3,955 |
) |
Notice Regarding Forward-Looking
Statements Information in this press release that is not
current or historical factual information may constitute forward
looking information within the meaning of securities laws. Implicit
in this information are assumptions regarding our future
operational results. These assumptions, although considered
reasonable by the company at the time of preparation, may prove to
be incorrect. Readers are cautioned that actual performance of the
company is subject to a number of risks and uncertainties,
including with respect to the commercial performance of NATESTO®
globally and in the U.S., and could differ materially from what is
currently expected as set out above. For more exhaustive
information on these risks and uncertainties you should refer to
our annual information form dated March 10, 2021 which is available
at www.sedar.com. Forward-looking information contained in this
press release is based on our current estimates, expectations and
projections, which we believe are reasonable as of the current
date. You should not place undue importance on forward-looking
information and should not rely upon this information as of any
other date. While we may elect to, we are under no obligation and
do not undertake to update this information at any particular time,
whether as a result of new information, future events or otherwise,
except as required by applicable securities law.
Company Contactir@aceruspharma.com
Investor Relations ContactChris WittyAcerus
Investor Relations (646) 438-9385cwitty@darrowir.com
Acerus Pharmaceuticals Corporation |
|
|
Condensed Interim Consolidated Statements of Financial
Position |
|
As at March 31, 2021 and December 31, 2020 |
|
|
Unaudited |
|
|
(expressed in thousands of U.S. dollars) |
|
|
|
|
March 31, 2021 |
|
December 31, 2020 |
|
|
|
|
|
ASSETS |
|
|
|
|
|
|
Current assets |
|
|
|
Cash |
$ |
5,167 |
|
$ |
9,153 |
|
|
Trade and
other receivables |
|
380 |
|
|
528 |
|
|
Contract
asset |
|
691 |
|
|
936 |
|
|
Inventory |
|
2,445 |
|
|
2,313 |
|
|
Prepaid and other assets |
|
1,157 |
|
|
1,104 |
|
Total current assets |
|
9,840 |
|
|
14,034 |
|
|
|
|
|
Property and equipment, net |
|
584 |
|
|
806 |
|
Intangible assets, net |
|
2,105 |
|
|
2,142 |
|
Total assets |
$ |
12,529 |
|
$ |
16,982 |
|
|
|
|
|
LIABILITIES AND SHAREHOLDERS' EQUITY
(DEFICIT) |
|
|
|
|
|
Current liabilities |
|
|
|
Accounts
payable and accrued liabilities |
$ |
7,171 |
|
$ |
5,435 |
|
|
Termination
fee payable |
|
2,776 |
|
|
- |
|
|
Current
portion of long-term debt |
|
2,602 |
|
|
1,439 |
|
|
Current
portion of lease liability |
|
205 |
|
|
229 |
|
Total current liabilities |
|
12,754 |
|
|
7,103 |
|
|
|
|
|
Termination fee payable |
|
3,428 |
|
|
- |
|
Long-term debt |
|
5,514 |
|
|
6,580 |
|
Derivative financial instruments |
|
208 |
|
|
139 |
|
Total liabilities |
|
21,904 |
|
|
13,822 |
|
|
|
|
|
Shareholders' equity (deficit) |
|
|
|
Share
capital |
$ |
198,163 |
|
$ |
198,163 |
|
|
Contributed
surplus |
|
13,726 |
|
|
13,435 |
|
|
Accumulated
other comprehensive loss |
|
(13,949 |
) |
|
(13,949 |
) |
|
Deficit |
|
(207,315 |
) |
|
(194,489 |
) |
Total shareholders' equity (deficit) |
|
(9,375 |
) |
|
3,160 |
|
Total liabilities & shareholders' equity
(deficit) |
$ |
12,529 |
|
$ |
16,982 |
|
Acerus Pharmaceuticals Corporation |
|
|
|
Condensed Interim Consolidated Statements of Loss and Comprehensive
Loss |
|
|
For the three months ended March 31, 2021 and 2020 |
|
|
|
Unaudited |
|
|
|
|
|
(expressed in thousands of U.S. dollars, except per share and share
data) |
|
|
|
|
|
|
For the
three months ended March 31, |
|
|
|
|
|
2021 |
|
|
|
2020 |
|
|
|
|
|
|
|
|
Revenue |
|
|
|
|
|
Product revenue |
|
|
$ |
234 |
|
|
$ |
145 |
|
Termination Fee |
|
|
|
(6,204 |
) |
|
|
- |
|
|
|
|
|
|
(5,970 |
) |
|
|
145 |
|
Cost of goods sold |
|
191 |
|
|
|
201 |
|
|
|
|
|
|
- |
|
|
|
- |
|
Gross margin (loss) |
|
|
|
(6,161 |
) |
|
|
(56 |
) |
|
|
|
|
|
|
|
Expenses |
|
|
|
|
|
|
Research and
development |
|
|
|
973 |
|
|
|
622 |
|
|
Selling, general and administrative |
|
|
5,287 |
|
|
|
3,577 |
|
Total operating expenses |
|
|
|
6,260 |
|
|
|
4,199 |
|
Operating loss |
|
|
|
(12,421 |
) |
|
|
(4,255 |
) |
|
|
|
|
|
|
|
Other expenses(income) |
|
|
|
|
|
|
Interest on long-term debt and other financing costs |
|
292 |
|
|
|
846 |
|
|
Interest
income |
|
|
|
(5 |
) |
|
|
(31 |
) |
|
Foreign
exchange gain |
|
|
|
(15 |
) |
|
|
(244 |
) |
|
Change in fair value of derivative financial instruments |
|
69 |
|
|
|
(163 |
) |
|
Loss on
modification of debt |
|
|
|
64 |
|
|
|
- |
|
Total other expenses |
|
|
|
405 |
|
|
|
408 |
|
Loss for the period before income taxes |
|
|
(12,826 |
) |
|
|
(4,663 |
) |
|
|
|
|
|
|
|
Income tax expense |
|
|
|
- |
|
|
|
- |
|
Net loss and comprehensive loss for the
period |
$ |
(12,826 |
) |
|
$ |
(4,663 |
) |
|
|
|
|
|
|
|
Loss per common share |
|
|
|
|
|
|
Basic and diluted net loss per common share |
$ |
(0.01 |
) |
|
$ |
(0.01 |
) |
|
|
|
|
|
|
|
Weighted average common shares outstanding |
|
|
|
|
|
Basic and
diluted |
|
|
|
1,537,588,081 |
|
|
|
656,423,941 |
|
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