HLS Therapeutics Announces Q1 2025 Financial Results
-
Total Product revenue grew 5% compared to Q1 2024, with growth across both the US and
Canada - Canadian Product revenue grew 13% (in local currency) compared to Q1 2024, driven by 34% year-over-year growth in Vascepa net sales
- Adjusted EBITDA grew 41% (or 78% excluding royalty revenue) compared to Q1 2024
-
HLS expands Cardiovascular portfolio by securing Canadian rights to NEXLETOL® and NEXLIZET® from
Esperion Therapeutics
Q1 2025 FINANCIAL HIGHLIGHTS (comparisons are to Q1 2024)
- Revenue was
$12.6 million , Adjusted EBITDA1 was$3.8 million and cash from operations was$3.5 million , compared to$12.5 million ,$2.7 million and$0.8 million , respectively. - Revenue for Vascepa increased 34% in local currency.
- Revenue for Clozaril Canada increased 1% in local currency.
- Revenue for Clozaril US increased 3%.
- Excluding cost of sales, operating expenses decreased 20%.
- Vascepa made a slightly positive contribution to Adjusted EBITDA in Q1 2025, compared to a negative
$1.6 million contribution in Q1 2024.
OTHER CORPORATE HIGHLIGHTS
- Announced an agreement with Esperion Therapeutics Inc. (NASDAQ:ESPR) to in-license and commercialize NEXLETOL2 and NEXLIZET2 in
Canada . See full press release details here. - Launched Normal Course Issuer Bid.
-
Christine Elliott , ex-Minister of Health inOntario , joined the Board of Directors.
"Our Q1 financial results demonstrated solid execution across the business, with product revenues and Adjusted EBITDA growing in line with expectations. We also made progress in building the foundation for future growth by expanding our product portfolio," said
"The strengthening of our financial position has created new opportunities to enhance shareholder value. We initiated a share buyback program in Q1 while continuing to pursue strategic growth opportunities such as portfolio expansion. Today's announcement of our agreement with
"These promising therapies are strategically aligned with our portfolio, complementing Vascepa and leveraging our established cardiovascular infrastructure in the Canadian market, which will minimize incremental costs. The products address significant unmet medical needs and represent a substantial growth opportunity. In Q4 2024, Esperion submitted New Drug Submissions to
Q1 2025 FINANCIAL REVIEW
The Company's Management's Discussion and Analysis and Consolidated Financial Statements for the three months ended
Revenue
|
|
Three months ended
|
||
|
|
|
2025 |
2024 |
|
|
|
|
|
Product sales |
|
|
|
|
Canada |
|
|
9,708 |
9,154 |
United States |
|
|
2,718 |
2,642 |
|
|
|
12,426 |
11,796 |
Royalty revenue |
|
|
197 |
677 |
|
|
|
12,623 |
12,473 |
Revenue for the three months ended
Product sales –
000's of CAD |
|
Three months ended
|
||||
|
|
|
|
2025 |
2024 |
% change |
|
|
|
|
|
|
|
Clozaril |
|
|
|
7,929 |
7,865 |
0.8 % |
Vascepa |
|
|
|
5,978 |
4,471 |
33.7 % |
Other |
|
|
|
32 |
13 |
|
|
|
|
|
13,939 |
12,349 |
12.9 % |
For the three months ended
Product Sales –
In the U.S. market, Clozaril revenue for the three months ended
Royalty revenues
As expected, royalty revenues for the three months ended
Operating Expenses
|
|
Three months ended
|
||
|
|
|
2025 |
2024 |
|
|
|
|
|
Cost of product sales |
|
|
2,398 |
1,774 |
Selling and marketing |
|
|
2,830 |
4,526 |
Medical, regulatory and patient support |
|
|
1,436 |
1,265 |
General and administrative |
|
|
2,139 |
2,201 |
|
|
|
8,803 |
9,766 |
Cost of product sales was up for the three months ended
Operating expenses in Q1 2025, excluding cost of product sales, decreased by 20% compared to Q1 2024, primarily due to lower selling and marketing expenses following the Company's discontinuation of co-promotional activities with its marketing partner in
Adjusted EBITDA1
|
|
Three months ended
|
||
|
|
|
2025 |
2024 |
|
|
|
|
|
Net loss for the period |
|
|
(4,436) |
(6,106) |
Stock-based compensation |
|
|
651 |
256 |
Amortization and depreciation |
|
|
5,360 |
5,919 |
Finance and related costs, net |
|
|
1,972 |
2,667 |
Other costs |
|
|
296 |
— |
Income tax recovery |
|
|
(23) |
(29) |
Adjusted EBITDA |
|
|
3,820 |
2,707 |
Adjusted EBITDA for the three months ended
The direct brand contribution from Clozaril to Adjusted EBITDA in Q1 2025 was
Net Loss
Net loss for the three months ended
Cash from Operations and Financial Position
Cash generated from operations for the three months ended
Total borrowings under the credit agreement at
During Q1 2025, HLS made principal payments on its term loan totaling
2025 OUTLOOK
Revenue projections for the Company's Canadian product portfolio are denominated in local currency to account for ongoing FX rate fluctuations. Importantly, the 2025 guidance fully incorporates all anticipated financial impacts from pre-launch activities related to the newly in-licensed NEXLETOL and NEXLIZET.
2025 financial targets are unchanged and as follows:
- Vascepa revenue of
C$26.5-28.5 million (18-26% growth) - Canada Clozaril sales of
C$35.5-36 million (flat year-over-year) - U.S. Clozaril sales of
$12-12.3 million (2-4% decline) - Royalty revenue of
$0.6-0.75 million (50-60% decline) - Consolidated Adjusted EBITDA of
$19.5-20.5 million (17-23% growth)
Future results could be impacted by continued exchange rate volatility.
Q1 2025 CONFERENCE CALL
HLS will hold a conference call today at
CONFERENCE ID: 41562
DATE: Thursday, May 8, 2025
TIME: 8:30 a.m. ET
WEBCAST LINK: https://app.webinar.net/EpY5Lzpk6d8
TRADITIONAL DIAL-IN NUMBER: 1-888-699-1199 or 1-416-945-7677
RAPIDCONNECT: To instantly join the conference call by phone, please use the following URL to easily register and be connected into the conference call automatically: https://emportal.ink/43us1qX
TAPED REPLAY: 1-888-660-6345 or 1-646-517-4150
REPLAY CODE: 41562#
The taped replay will be available for 14 days and the archived webcast will be available for 365 days.
A link to the live audio webcast of the conference call will also be available on the events page of the investors section of
ABOUT
Formed in 2015, HLS is a pharmaceutical company focused on the acquisition and commercialization of late-stage development, commercial stage promoted and established branded pharmaceutical products in the North American markets. HLS's focus is on products targeting the central nervous system and cardiovascular therapeutic areas. HLS's management team is composed of seasoned pharmaceutical executives with a strong track record of success in these therapeutic areas and at managing products in each of these lifecycle stages. For more information visit: www.hlstherapeutics.com
1
CAUTIONARY NOTE REGARDING NON-IFRS MEASURES
This press release refers to certain non-IFRS measures. These measures are not recognized measures under IFRS, do not have a standardized meaning prescribed by IFRS and are therefore unlikely to be comparable to similar measures presented by other companies. Rather, these measures are provided as additional information to complement those IFRS measures by providing further understanding of HLS's results of operations from management's perspective. Accordingly, they should not be considered in isolation nor as a substitute for analysis of HLS's financial information reported under IFRS. HLS uses non-IFRS measures to provide investors with supplemental measures of its operating performance and thus highlight trends in its core business that may not otherwise be apparent when relying solely on IFRS financial measures. HLS also believes that securities analysts, investors and other interested parties frequently use non-IFRS measures in the evaluation of issuers. HLS's management also uses non-IFRS measures in order to facilitate operating performance comparisons from period to period, prepare annual operating budgets and assess HLS's ability to meet its future debt service, capital expenditure and working capital requirements.
In particular, management uses Adjusted EBITDA as a measure of HLS's performance. To reconcile net income (loss) for the period with Adjusted EBITDA, each of (i) "stock-based compensation", (ii) "amortization and depreciation", (iii) "finance and related costs, net", (iv) "other costs (income)", and (v) "income tax expense (recovery)" appearing in the Consolidated Statement of Net Income (Loss) are added to net income (loss) for the period to determine Adjusted EBITDA. Adjusted EBITDA does not have any standardized meaning prescribed by IFRS and is not necessarily comparable to similar measures presented by other companies. Adjusted EBITDA should not be considered in isolation or as a substitute for net income (loss) prepared in accordance with IFRS as issued by the IASB .
REFERENCES
2: NEXLETOL® (bempedoic acid) and NEXLIZET® (bempedoic acid and ezetimibe) are the commercial brand names in the
FORWARD LOOKING INFORMATION
This release includes forward-looking statements regarding HLS and its business. Such statements are based on the current expectations and views of future events of HLS's management. In some cases the forward-looking statements can be identified by words or phrases such as "may", "will", "expect", "plan", "anticipate", "intend", "potential", "estimate", "believe" or the negative of these terms, or other similar expressions intended to identify forward-looking statements, including, among others, statements with respect to HLS's pursuit of additional product and pipeline opportunities in certain therapeutic markets, statements regarding growth opportunities, expectations regarding financial performance, and the NCIB and ASPP. The forward-looking events and circumstances discussed in this release may not occur and could differ materially as a result of known and unknown risk factors and uncertainties affecting HLS, including risks relating to the specialty pharmaceutical industry, risks related to the regulatory approval process, economic factors and many other factors beyond the control of HLS. Forward-looking statements and information by their nature are based on assumptions and involve known and unknown risks, uncertainties and other factors which may cause HLS's actual results, performance or achievements, or industry results, to be materially different from any future results, performance or achievements expressed or implied by such forward-looking statement or information. Accordingly, readers should not place undue reliance on any forward-looking statements or information. A discussion of the material risks and assumptions associated with this release can be found in the Company's Annual Information Form dated
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|||
CONSOLIDATED STATEMENTS OF FINANCIAL POSITION |
|||
Unaudited |
|||
[in thousands of |
|
|
|
|
|
As at |
As at |
|
|
|
|
|
|
|
|
ASSETS |
|
|
|
Current |
|
|
|
Cash |
|
17,734 |
17,456 |
Accounts receivable |
|
7,732 |
7,454 |
Inventories |
|
7,483 |
9,058 |
Income taxes recoverable |
|
71 |
71 |
Other current assets |
|
1,048 |
1,361 |
Total current assets |
|
34,068 |
35,400 |
Property, plant and equipment |
|
972 |
997 |
Intangible assets |
|
117,177 |
122,122 |
Deferred tax asset |
|
1,200 |
857 |
Other non-current assets |
|
530 |
528 |
Total assets |
|
153,947 |
159,904 |
|
|
|
|
LIABILITIES AND SHAREHOLDERS' EQUITY |
|
|
|
Current |
|
|
|
Accounts payable and accrued liabilities |
|
8,682 |
8,709 |
Provisions |
|
8,561 |
8,367 |
Debt and other liabilities |
|
6,203 |
5,317 |
Income taxes payable |
|
394 |
152 |
Total current liabilities |
|
23,840 |
22,545 |
Debt and other liabilities |
|
59,181 |
61,944 |
Deferred tax liability |
|
4,128 |
4,074 |
Total liabilities |
|
87,149 |
88,563 |
|
|
|
|
Shareholders' equity |
|
|
|
Share capital |
|
260,136 |
260,595 |
Contributed surplus |
|
14,893 |
15,136 |
Accumulated other comprehensive loss |
|
(9,898) |
(10,210) |
Deficit |
|
(198,333) |
(194,180) |
Total shareholders' equity |
|
66,798 |
71,341 |
Total liabilities and shareholders' equity |
|
153,947 |
159,904 |
|
|||||||||
CONSOLIDATED STATEMENTS OF LOSS |
|||||||||
Unaudited |
|||||||||
[in thousands of |
|
|
|||||||
|
|
Three months ended
|
|||||||
|
|
|
|
2025 |
2024 |
||||
|
|
|
|
|
|
||||
Revenue |
|
|
|
12,623 |
12,473 |
||||
|
|
|
|
|
|
||||
Expenses |
|
|
|
|
|
||||
Cost of product sales |
|
|
|
2,398 |
1,774 |
||||
Selling and marketing |
|
|
|
2,830 |
4,526 |
||||
Medical, regulatory and patient support |
|
|
|
1,436 |
1,265 |
||||
General and administrative |
|
|
|
2,139 |
2,201 |
||||
Stock-based compensation |
|
|
|
651 |
256 |
||||
Amortization and depreciation |
|
|
|
5,360 |
5,919 |
||||
Finance and related costs, net |
|
|
|
1,972 |
2,667 |
||||
Other costs |
|
|
|
296 |
— |
||||
Loss before income taxes |
|
|
|
(4,459) |
(6,135) |
||||
Income tax recovery |
|
|
|
(23) |
(29) |
||||
Net loss for the period |
|
|
|
(4,436) |
(6,106) |
||||
|
|
|
|
||||||
Net loss per share: |
|
|
|
||||||
Basic and diluted |
|
|
|
|
|
|
|||||||||
|
|||||||||
CONSOLIDATED STATEMENTS OF COMPREHENSIVE LOSS |
|||||||||
Unaudited |
|||||||||
[in thousands of |
|
|
|||||||
|
|
Three months ended
|
|||||||
|
|
|
2025 |
2024 |
|||||
|
|
|
|
|
|||||
Net loss for the period |
|
|
(4,436) |
(6,106) |
|||||
|
|
|
|
|
|||||
Item that may be reclassified subsequently to net loss |
|
|
|
|
|||||
Unrealized foreign currency translation adjustment |
|
|
312 |
(2,373) |
|||||
Comprehensive loss for the period |
|
|
(4,124) |
(8,479) |
|
||||||
INTERIM CONSOLIDATED STATEMENTS OF CHANGES IN SHAREHOLDERS' EQUITY |
||||||
Unaudited |
||||||
[in thousands of |
|
|
|
|
|
|
|
|
Share capital |
Contributed surplus |
Accumulated other |
Deficit |
Total |
|
|
|
|
|
|
|
Balance, |
|
260,595 |
15,136 |
(10,210) |
(194,180) |
71,341 |
Shares repurchased |
|
(459) |
— |
— |
283 |
(176) |
Change in share purchase obligation |
|
— |
(495) |
— |
— |
(495) |
Stock option expense |
|
— |
252 |
— |
— |
252 |
Net loss for the period |
|
— |
— |
— |
(4,436) |
(4,436) |
Unrealized foreign currency |
|
— |
— |
312 |
— |
312 |
Balance, |
|
260,136 |
14,893 |
(9,898) |
(198,333) |
66,798 |
|
|
|
|
|
|
|
Balance, |
|
262,127 |
13,865 |
(2,838) |
(175,457) |
97,697 |
Shares repurchased |
|
(768) |
— |
— |
485 |
(283) |
Stock option expense |
|
— |
131 |
— |
— |
131 |
Net loss for the period |
|
— |
— |
— |
(6,106) |
(6,106) |
Unrealized foreign currency |
|
— |
— |
(2,373) |
— |
(2,373) |
Balance, |
|
261,359 |
13,996 |
(5,211) |
(181,078) |
89,066 |
|
|||
INTERIM CONSOLIDATED STATEMENTS OF CASH FLOWS |
|||
Unaudited |
|||
[in thousands of |
|
|
|
|
|
Three months ended
|
|
|
|
2025 |
2024 |
|
|
|
|
OPERATING ACTIVITIES |
|
|
|
Net loss for the period |
|
(4,436) |
(6,106) |
Adjustments to reconcile net loss to cash provided by operating activities |
|
|
|
Stock-based compensation |
|
651 |
256 |
Amortization and depreciation |
|
5,360 |
5,919 |
Accreted interest |
|
308 |
282 |
Fair value adjustment on financial assets and liabilities |
|
— |
187 |
Deferred income taxes |
|
(289) |
(61) |
Net change in non-cash working capital balances related to operations |
|
1,949 |
301 |
Cash provided by operating activities |
|
3,543 |
778 |
|
|
|
|
INVESTING ACTIVITIES |
|
|
|
Additions to property, plant and equipment |
|
(21) |
(2) |
Cash used in investing activities |
|
(21) |
(2) |
|
|
|
|
FINANCING ACTIVITIES |
|
|
|
Shares repurchased |
|
(176) |
(283) |
Repayment of credit agreement borrowing |
|
(2,960) |
(2,075) |
Debt costs |
|
— |
(533) |
Lease payments |
|
(143) |
(143) |
Cash used in financing activities |
|
(3,279) |
(3,034) |
|
|
|
|
Net increase (decrease) in cash during the period |
|
243 |
(2,258) |
Foreign currency translation |
|
35 |
(251) |
Cash, beginning of period |
|
17,456 |
21,952 |
Cash, end of period |
|
17,734 |
19,443 |
|
|
|
SOURCE