(All figures are presented in U.S.
dollars)
- Strong growth capital available with $36.3 million in cash and cash
equivalents
- Net income increased by 32% year-over-year to $5.7 million
- EPS increased 35% year-over-year to $0.23 per share
MISSISSAUGA, ON, Aug. 10,
2023 /CNW/ - Cipher Pharmaceuticals Inc. (TSX:
CPH) ("Cipher" or "the Company") today announced its
financial and operating results for the three and six month periods
ended June 30, 2023.
Q2 2023 Financial Highlights
(All figures in U.S.
dollars, compared to Q2 2022, unless otherwise noted)
- MOB-015 pipeline product for nail fungus treatment obtained
European Union approval
- Commercial launch of Epuris in Mexico through partnerships with Italmex &
Galephar
- Total revenue was $5.3 million
compared to $5.6 million in Q2
2022
- Licensing revenue increased 6% to $2.2
million compared to $2.0
million in Q2 2022
- Adjusted EBITDA1 was $3.1
million compared to $3.6
million in Q2 2022
- Ended the quarter with $36.3
million in cash (CDN$48.12) or $1.43 per share (CDN $1.902)
Management Commentary
Craig Mull, Interim CEO
commented, "I am proud to announce further developments on our
product pipeline, whereby Moberg Pharma recently obtained a
significant European Union regulatory milestone, paving the way for
commercial launch of their MOB-015 nail fungus treatment across 13
countries in Europe. Cipher holds
the exclusive rights to MOB-015 in Canada and we believe approval in the European
Union highly de-risks the eventual regulatory approval in
Canada, which is a market
opportunity in excess of CDN $80
million.
We also are proud to announce the official launch of Epuris in
Mexico, making our isotretinoin
product available to the many Mexicans who suffer from severe acne.
In May 2023, Epuris was commercially
launched through Cipher's strong established partnerships with
Galephar Pharmaceutical Research and Italmex Pharma S.A. Epuris has
established itself as the #1 prescribed isotretinoin product
dermatologists rely on in Canada,
and we believe this is a tremendous step in further growth of the
Epuris brand."
Bryan Jacobs, CFO
commented, "During the second quarter, our business
performed as expected with sequentially strong revenue, earnings
and cash flows from operations compared to trailing quarters. Our
EBITDA and Adjusted EBITDA of $3.1
million during the quarter was highly correlated to the
increase of our cash on hand by $2.9
million, which is indicative of a well managed business.
Cipher ended the quarter with $36.3
million in cash with access to a $35
million revolving credit facility, placing us in a
formidable position to drive future growth of our
business."
Q2 2023 Financial Review
(All figures are in U.S.
dollars)
- Total revenue was $5.3 million in
Q2 2023, compared to $5.6 million in
Q2 2022.
- Licensing revenue was $2.2
million in Q2 2023, compared to $2.0
million in Q2 2022.
- Product revenue was $3.1 million
in Q2 2023, compared to $3.5 million
in Q2 2022.
- Net income was $3.1 million, or
$0.12 per diluted share in Q2 2023,
compared to $2.2 million, or
$0.08 per diluted share in Q2
2022.
- Adjusted EBITDA for Q2 2023 was $3.1
million, compared to $3.6
million in Q2 2022.
- The Company had $36.3 million in
cash and no debt as of the end Q2 2023.
- Cipher generated $2.9 million of
additional cash on hand in Q2 2023 (YTD $7.5
million).
Business Strategy & Outlook
Cipher anticipates executing on its business strategy in 2023 to
enhance long term value, including:
- Focusing on acquiring cash flow positive pharmaceutical assets
to further diversity our product portfolio
- Continuing to collaborate with our partners to further
development on our product pipeline, including MOB-015 for the
treatment of nail fungus and CF-101 for the treatment of moderate
to severe plaque psoriasis
- Advancing our studies on DTR-001, our pipeline product for the
removal of tattoos
- Continuing to pursue opportunities to enhance long-term
shareholder value
- Operating the business in an efficient and prudent manner to
deliver continued earnings, being our management philosophy
Corporate Developments
- On July 5, 2023, Cipher announced
that its partner, Moberg Pharma AB, has obtained European Union
approval for its product MOB-015 for the treatment of nail fungus,
paving the way for their commercial launch across 13 countries in
Europe. Cipher believes this is an
important precursor to the eventual approval in North America and Canada
- In May 2023, the Epuris product
was launched commercially by Galephar's commercial partner in
Mexico, Italmex. For the three
months ended June 30, 2023, royalty
revenue of $0.1 million was earned on
initial sales of Epuris in Mexico
- In June 2023, Cipher's partner,
Canfite Biopharma announced it had received a positive view from
the FDA with respect to its registration plan for the pivotal Phase
III clinical trial of CF-101 for the treatment of moderate to
severe psoriasis
- In June 2023, the Company
bolstered the pharmaceutical experience and expertise of its board
with the appointment of two new directors to the Company's board of
directors, Mr. Douglas Deeth and Dr.
Hubert Walinski
Financial Statements and MD&A
Cipher's Financial Statements for the three and six month
periods ended June 30, 2023, and Management's Discussion
and Analysis (the "MD&A") for the three and six month
periods ended June 30, 2023, are available on the
Company's website at www.cipherpharma.com in the
"Investors" section under "Financial Reports" and on SEDAR+
at www.sedarplus.ca.
Notice of Conference Call
Cipher will hold a conference call on August 11, 2023,
at 8:30 a.m. (ET) to discuss its financial results and
other corporate developments. To access the conference call by
telephone, dial (416) 764-8650 or (888) 664-6383 and use
conference ID 71994934.
A live audio webcast will be available
at https://app.webinar.net/l8n1YB8qokM
- or the Investor Relations section of the Company's website at
http://www.cipherpharma.com.
- An archived replay of the webcast will be available until
August 18, 2023.
About Cipher Pharmaceuticals Inc.
Cipher Pharmaceuticals (TSX: CPH) is a specialty pharmaceutical
company with a robust and diversified portfolio of commercial and
early to late-stage products. Cipher acquires products that fulfill
unmet medical needs, manages the required clinical development and
regulatory approval process, and currently markets those products
either directly in Canada or indirectly through partners
in Canada, the U.S., and South America. For more
information, visit www.cipherpharma.com.
Forward-Looking Statements and Non-IFRS Measures
This document includes forward-looking statements within the
meaning of applicable securities laws. These forward-looking
statements include, among others, statements with respect to our
beliefs, plans, expectations, anticipations, estimates and
intentions. The words "may", "will", "could", "should", "would",
"suspect", "outlook", "believe", "plan", "anticipate", "estimate",
"expect", "intend", "forecast", "objective", "hope" and "continue"
(or the negative thereof), and words and expressions of similar
import, are intended to identify forward-looking
statements.
By their very nature, forward-looking statements involve
inherent risks and uncertainties, both general and specific, which
give rise to the possibility that predictions, forecasts,
projections and other forward-looking statements will not be
achieved. Certain material factors or assumptions are applied in
making forward-looking statements and actual results may differ
materially from those expressed or implied in such statements. We
caution readers not to place undue reliance on these statements as
a number of important factors, many of which are beyond our
control, could cause our actual results to differ materially from
the beliefs, plans, objectives, expectations, anticipations,
estimates and intentions expressed in such forward-looking
statements. These factors include, but are not limited to, the
extent and impact of the coronavirus (COVID-19) outbreak on our
business including any impact on our contract manufacturers and
other third party service providers, our ability to enter into
development, manufacturing and marketing and distribution
agreements with other pharmaceutical companies and keep such
agreements in effect; our dependency on a limited number of
products; our dependency on protection from patents that will
expire; integration difficulties and other risks if we acquire or
in-license technologies or product candidates; reliance on third
parties for the marketing of certain products; the product approval
process is highly unpredictable; the timing of completion of
clinical trials, regulatory submissions and regulatory approvals;
reliance on third parties to manufacture our products and events
outside of our control that could adversely impact the ability of
our manufacturing partners to supply products to meet our demands;
we may be subject to future product liability claims; unexpected
product safety or efficacy concerns may arise; we generate license
revenue from a limited number of distribution and supply
agreements; the pharmaceutical industry is highly competitive;
requirements for additional capital to fund future operations;
products in Canada may be subject
to pricing regulation; dependence on key managerial personnel and
external collaborators; no assurance that we will receive
regulatory approvals in the U.S., Canada or any other jurisdictions and current
uncertainty surrounding health care regulation in the U.S.; certain
of our products are subject to regulation as controlled substances;
limitations on reimbursement in the healthcare industry; limited
reimbursement for products by government authorities and
third-party payor policies; products may not be included on list of
drugs approved for use in hospitals; hospital customers may make
late payments or not make any payments; various laws pertaining to
health care fraud and abuse; reliance on the success
of strategic investments and partnerships; the publication of
negative results of clinical trials; unpredictable development
goals and projected time frames; rising insurance costs; ability to
enforce covenants not to compete; risks associated with the
industry in which we operate; we may be unsuccessful in evaluating
material risks involved in completed and future acquisitions; we
may be unable to identify, acquire or integrate acquisition targets
successfully; legacy risks from operations conducted in the U.S.;
inability to meet covenants under our long term debt arrangement;
compliance with privacy and security regulation; our policies
regarding returns, allowances and chargebacks may reduce revenues;
certain current and future regulations could restrict our
activities; additional regulatory burden and controls over
financial reporting; reliance on third parties to perform certain
services; general commercial litigation, class actions, other
litigation claims and regulatory actions; the difficulty for
shareholders to realize in the United
States upon judgments of U.S. courts predicated upon civil
liability of the Company and its directors and officers who are not
residents of the United States;
the potential violation of intellectual property rights of third
parties; our efforts to obtain, protect or enforce our patents and
other intellectual property rights related to our products; changes
in U.S., Canadian or foreign patent laws; litigation in the
pharmaceutical industry concerning the manufacture and supply of
novel and generic versions of existing drugs; inability to protect
our trademarks from infringement; shareholders may be further
diluted if we issue securities to raise capital; volatility of our
share price; the fact that we have a significant shareholder; we do
not currently intend to pay dividends; our operating results may
fluctuate significantly; and our debt obligations will have
priority over the common shares of the Company in the event of a
liquidation, dissolution or winding up.
We caution that the foregoing list of important factors that
may affect future results is not exhaustive. When reviewing our
forward-looking statements, investors and others should carefully
consider the foregoing factors and other uncertainties and
potential events. Additional information about factors that may
cause actual results to differ materially from expectations, and
about material factors or assumptions applied in making
forward-looking statements, may be found in the "Risk Factors"
section of the Company's Annual Information Form for the year ended
December 31, 2022, and elsewhere in
our filings with Canadian securities regulators. Except as required
by Canadian securities law, we do not undertake to update any
forward-looking statements, whether written or oral, that may be
made from time to time by us or on our behalf; such statements
speak only as of the date made. The forward-looking statements
included herein are expressly qualified in their entirety by this
cautionary language.
- EBITDA and adjusted EBITDA are non-IFRS financial measures.
The term EBITDA (earnings before interest, taxes, depreciation and
amortization,) does not have any standardized meaning under IFRS
and therefore may not be comparable to similar measures presented
by other companies. Rather, these measures are provided as
additional information to complement IFRS measures by providing a
further understanding of operations from management's perspective.
The Company defines Adjusted EBITDA as earnings before interest
expense, income taxes, depreciation of property and equipment,
amortization of intangible assets, non-cash share-based
compensation, changes in fair value of derivative financial
instruments, provision for legal settlement, loss on disposal of
assets and loss on extinguishment of lease, impairment of
intangible assets, restructuring costs and foreign exchange gains
and losses from the translation of Canadian cash balances.
- At the June 30, 2023 exchange
rate – 1.3240
The following is a summary of how EBITDA and Adjusted EBITDA are
calculated:
(IN THOUSANDS OF U.S. DOLLARS,
except for per share amounts)
|
Three months
ended
June 30, 2023
|
Three months
ended
June 30, 2022
|
Six months
ended
June 30, 2023
|
Six months
ended
June 30, 2022
|
|
$
|
$
|
$
|
$
|
Income and
comprehensive income
|
3,071
|
2,152
|
5,697
|
4,302
|
Add back:
|
|
|
|
|
Depreciation and
amortization
|
342
|
155
|
685
|
310
|
Interest
income
|
(427)
|
(33)
|
(782)
|
(40)
|
Income
taxes
|
99
|
1,175
|
181
|
1,948
|
EBITDA
|
3,085
|
3,449
|
5,781
|
6,520
|
Unrealized foreign
exchange (gain) loss
|
(448)
|
75
|
(455)
|
58
|
Restructuring
costs
|
231
|
—
|
269
|
—
|
Share-based
compensation
|
209
|
47
|
653
|
85
|
Adjusted
EBITDA
|
3,077
|
3,571
|
6,248
|
6,663
|
Adjusted EBITDA per
share – basic
|
0.12
|
0.14
|
0.25
|
0.26
|
Adjusted EBITDA per
share – dilutive
|
0.12
|
0.14
|
0.24
|
0.26
|
Condensed interim consolidated statements of income and
comprehensive income
|
Three months
ended June 30,
|
Six months
ended June 30,
|
|
2023
|
2022
|
2023
|
2022
|
|
$
|
$
|
$
|
$
|
|
|
|
|
|
Revenue
|
|
|
|
|
Licensing
revenue
|
2,170
|
2,046
|
3,846
|
4,144
|
Product
revenue
|
3,118
|
3,512
|
6,328
|
6,829
|
Net
revenue
|
5,288
|
5,558
|
10,174
|
10,973
|
|
|
|
|
|
Operating
expenses
|
|
|
|
|
Cost of products
sold
|
1,061
|
1,072
|
2,038
|
2,195
|
Research and
development
|
97
|
1
|
100
|
66
|
Depreciation and
amortization
|
342
|
155
|
685
|
310
|
Selling, general and
administrative
|
1,493
|
961
|
2,710
|
2,134
|
Total operating
expenses
|
2,993
|
2,189
|
5,533
|
4,705
|
|
|
|
|
|
Other (income)
expenses
|
|
|
|
|
Interest
income
|
(427)
|
(33)
|
(782)
|
(40)
|
Unrealized foreign
exchange (gain) loss
|
(448)
|
75
|
(455)
|
58
|
Total other (income)
expenses
|
(875)
|
42
|
(1,237)
|
18
|
|
|
|
|
|
Income before income
taxes
|
3,170
|
3,327
|
5,878
|
6,250
|
|
|
|
|
|
Current income tax
(recovery) expense
|
115
|
1,099
|
212
|
1,823
|
Deferred income tax
(recovery) expense
|
(16)
|
76
|
(31)
|
125
|
Total income tax
(recovery) expense
|
99
|
1,175
|
181
|
1,948
|
|
|
|
|
|
Net income and
comprehensive income for the period
|
3,071
|
2,152
|
5,697
|
4,302
|
|
|
|
|
|
|
|
|
|
|
Income per
share
|
|
|
|
|
Basic
|
0.12
|
0.08
|
0.23
|
0.17
|
Diluted
|
0.12
|
0.08
|
0.22
|
0.16
|
Condensed interim consolidated statements of financial
position
|
As at June 30,
|
As at December
31,
|
|
2023
|
2022
|
|
$
|
$
|
Assets
|
|
|
|
|
|
Current
assets
|
|
|
Cash and cash
equivalents
|
36,338
|
28,836
|
Accounts
receivable
|
5,824
|
6,802
|
Inventory
|
2,864
|
2,152
|
Prepaid expenses and
other assets
|
224
|
371
|
Total current
assets
|
45,250
|
38,161
|
Property and equipment,
net
|
441
|
481
|
Intangible assets,
net
|
2,126
|
2,754
|
Goodwill
|
15,706
|
15,706
|
Deferred tax
assets
|
17,089
|
16,674
|
Total
assets
|
80,612
|
73,776
|
|
|
|
Liabilities and
shareholders' equity
|
|
|
|
|
|
Current
liabilities
|
|
|
Accounts payable and
accrued liabilities
|
4,504
|
4,107
|
Income taxes
payable
|
5,230
|
4,904
|
Contract
liability
|
292
|
257
|
Current portion of
lease obligation
|
104
|
101
|
Total current
liabilities
|
10,130
|
9,369
|
Lease
obligation
|
282
|
327
|
Total
liabilities
|
10,412
|
9,696
|
|
|
|
Shareholders'
equity
|
|
|
Share
capital
|
18,281
|
17,719
|
Contributed
surplus
|
5,471
|
5,358
|
Accumulated other
comprehensive loss
|
(9,514)
|
(9,514)
|
Retained
earnings
|
55,962
|
50,517
|
Total shareholders'
equity
|
70,200
|
64,080
|
Total liabilities
and shareholders' equity
|
80,612
|
73,776
|
SOURCE Cipher Pharmaceuticals Inc.