BioSyent Releases Financial Results for Q2 and H1 2025

BioSyent Releases Financial Results for Q2 and H1 2025

BioSyent Inc. ("BioSyent", TSX Venture: RX) released today its financial results for the three months (Q2) and six months (H1) ended June 30, 2025. Key highlights include:

(CAD) Q2 2025 % Change
vs.

Q2 2024
H1 2025 % Change
vs.

H1 2024
Trailing Twelve
Months
(TTM)
June 30, 2025
% Change
vs.

TTM
June 30, 2024
Canadian Pharma Sales 9,327,224 +9% 18,486,876 +15% 35,336,401 +12%
International Pharma Sales 445,614 +183% 1,980,830 +1160% 2,753,588 129%
Total Company Sales 10,179,296 +14% 21,158,256 +27% 39,510,951 +17%
EBITDA 1 2,760,149 +35% 5,961,796 +40% 11,052,544 +26%
Net Income After Taxes (NIAT) 2,018,171 +28% 4,338,104 +30% 8,259,192 +16%
Fully Diluted EPS 0.18 +31% 0.38 +33% 0.72 +20%
  • Return on Average Equity for TTM June 30, 2025 was 23% as compared to 21% for TTM June 30, 2024
  • During H1 2025, repurchased for cancellation a total of 19,500 common shares under a Normal Course Issuer Bid (NCIB)
  • Paid quarterly cash dividends of $0.05 per common share on March 14, 2025 and June 13, 2025
  • Declared subsequent cash dividend of $0.05 per common share to be paid on September 15, 2025

"Each of our Canadian Pharma, International Pharma, and Legacy businesses continued to perform well during Q2 2025, delivering 14% sales growth and 28% net profit growth overall," commented Mr. René Goehrum, President and CEO of BioSyent. "Led by FeraMAX ® Pd and Tibella ® (tibolone), Canadian Pharma sales grew by 9% overall for the quarter, in spite of uncertainty in the Canadian economy from the ongoing threat of tariffs. Our International Tibelia ® (tibolone) business also continued to perform to our expectations in Q2 2025, with year-to-date incremental revenues of $1.3 million following our September 2024 acquisition of the worldwide rights to this product. Though our overall gross margins have tightened with changes in product mix, our net profit margin improved to 21% of sales in H1 2025 from 20% in the comparative period with an overall reduction in our operating expense ratio."

"With momentum in all of our businesses as we enter the second half of 2025, I look forward to reporting on our continued progress. We remain committed to long-term value creation through portfolio diversification and profitable growth."

The CEO's presentation on the Q2 and H1 2025 Results is available at the following link: www.biosyent.com/investors/

The Company's Interim Unaudited Condensed Consolidated Financial Statements and Management's Discussion and Analysis for the three and six months ended June 30, 2025 and 2024 will be posted on www.sedarplus.ca on August 21, 2025.

For a direct market quote for the TSX Venture Exchange and other Company financial information, please visit www.tmxmoney.com .

About BioSyent Inc.

Listed on the TSX Venture Exchange under the trading symbol "RX", BioSyent is a profitable growth-oriented specialty pharmaceutical company focused on in-licensing or acquiring innovative pharmaceutical and other healthcare products that have been successfully developed, are safe and effective, and have a proven track record of improving the lives of patients. BioSyent supports the healthcare professionals that treat these patients by marketing its products through its community, specialty and international business units.

As of the date of this press release, the Company has 11,260,794 common shares outstanding.

BioSyent Inc.
Interim Unaudited Condensed Consolidated Statements of Comprehensive Income
In Canadian Dollars Q2 2025 Q2 2024 % Change H1 2025 H1 2024 % Change
Net Revenues 10,179,296 8,944,566 14 % 21,158,256 16,678,202 27 %
Cost of Goods Sold 2,266,734 1,873,731 21 % 4,908,502 3,463,493 42 %
Gross Profit 7,912,562 7,070,835 12 % 16,249,754 13,214,709 23 %
Operating Expenses and Finance Income/Costs 5,166,751 4,920,781 5 % 10,347,572 8,658,224 20 %
Net Income Before Tax 2,745,811 2,150,054 28 % 5,902,182 4,556,485 30 %
Tax (including Deferred Tax) 727,640 569,765 28 % 1,564,078 1,207,469 30 %
Net Income After Tax 2,018,171 1,580,289 28 % 4,338,104 3,349,016 30 %
Net Income After Tax % to Net Revenues 20 % 18 % 21 % 20 %
EBITDA 2,760,149 2,048,071 35 % 5,961,796 4,252,264 40 %
EBITDA % to Net Revenues 27 % 23 % 28 % 25 %
  1. EBITDA is a Non-IFRS Financial Measure. The term EBITDA does not have any standardized meaning under International Financial Reporting Standards (IFRS) and therefore may not be comparable to similar measures presented by other companies. The Company defines EBITDA as earnings before interest income or expense, income taxes, depreciation and amortization.

BioSyent Inc.
Interim Unaudited Condensed Consolidated Statements of Financial Position
AS AT June 30, 2025 December 31, 2024 % Change
ASSETS
Cash, cash equivalents and short-term investments $ 20,364,392 $ 15,940,971 28 %
Trade and other receivables 4,867,796 2,906,829 67 %
Inventory 4,860,613 5,328,086 -9 %
Prepaid expenses and deposits 443,573 201,971 120 %
Derivative asset - 5,790 -100 %
Loans receivable - current 56,098 87,433 -36 %
CURRENT ASSETS 30,592,472 24,471,080 25 %
Long term investments 6,497,025 10,103,571 -36 %
Loans receivable - current 84,093 141,140 -40 %
Deferred tax asset 371,104 401,166 -7 %
Property and equipment 1,104,639 1,200,992 -8 %
Intangible assets 4,846,156 5,041,501 -4 %
TOTAL NON CURRENT ASSETS 12,903,017 16,888,370 -24 %
TOTAL ASSETS $ 43,495,489 $ 41,359,450 5 %
LIABILITIES AND SHAREHOLDERS' EQUITY
CURRENT LIABILITIES $ 5,042,364 $ 5,405,106 -7 %
NON CURRENT LIABILITIES 852,372 951,159 -10 %
Long term debt - - 0 %
Total Equity 37,600,753 35,003,185 7 %
TOTAL LIABILITIES AND SHAREHOLDERS' EQUITY $ 43,495,489 $ 41,359,450 5 %

For further information please contact:
Mr. René C. Goehrum
President and CEO
BioSyent Inc.
E-Mail: investors@biosyent.com
Phone: 905-206-0013
Web: www.biosyent.com

This press release may contain information or statements that are forward-looking. The contents herein represent our judgment, as at the release date, and are subject to risks and uncertainties that may cause actual results or outcomes to be materially different from the forward-looking information or statements. Potential risks may include, but are not limited to, those associated with clinical trials, product development, future revenue, operations, profitability and obtaining regulatory approvals. Neither TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in the policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this press release.


Primary Logo

News Provided by GlobeNewswire via QuoteMedia

RX:CC
The Conversation (0)
InMed Pharmaceuticals Announces Positive Data from Human Brain Organoid Neuroinflammation Models Supporting the INM-901 Alzheimer's Disease Program

InMed Pharmaceuticals Announces Positive Data from Human Brain Organoid Neuroinflammation Models Supporting the INM-901 Alzheimer's Disease Program

Human Organoid Data Supports the Therapeutic Rationale for INM-901 Program Ahead of Human Clinical TrialsConsistent Anti-Inflammatory Effects Demonstrate Translation from Animal Models to Three-Dimensional Human Brain Tissue SystemsInMed Pharmaceuticals Inc. (NASDAQ: INM) ("InMed" or the... Keep Reading...
SVN-114 selected as the lead candidate for PTSD discovery programme

SVN-114 selected as the lead candidate for PTSD discovery programme

Novel compound from patent-pending SVN-SDN-14 series targeting a major global mental health disorder

Solvonis Therapeutics plc (LSE: SVNS), an emerging biopharmaceutical company developing novel small-molecule therapeutics for high-burden central nervous system ("CNS") disorders, announces the selection of SVN-114 as the lead candidate from the Company's proprietary SVN-SDN-14 discovery... Keep Reading...
InMed Provides Update on Pharmaceutical Development Programs - Advancing Lead Drug Candidates Towards IND and Clinical Trial

InMed Provides Update on Pharmaceutical Development Programs - Advancing Lead Drug Candidates Towards IND and Clinical Trial

Advancing Alzheimer's and Age-Related Macular Degeneration Programs Toward FDA Engagement and IND-Enabling ActivitiesTargeting Initiation of Phase 1 Clinical Trial in Alzheimer's Disease in 2027InMed Pharmaceuticals Inc. (NASDAQ: INM) ("InMed" or the "Company"), a pharmaceutical company focused... Keep Reading...
InMed Provides Update on BayMedica Operations and Strengthens Focus on Pharmaceutical Development Pipeline

InMed Provides Update on BayMedica Operations and Strengthens Focus on Pharmaceutical Development Pipeline

InMed Pharmaceuticals Inc. (NASDAQ: INM) ("InMed" or the "Company"), a pharmaceutical company focused on developing a pipeline of disease-modifying small molecule drug candidates that target CB1CB2 receptors, today announced an update regarding BayMedica LLC ("BayMedica"), a wholly owned... Keep Reading...
Box of Moderna COVID-19 vaccine vials with red caps and labels.

Moderna to Pay US$950 Million to Settle COVID-19 Vaccine Patent Dispute

Moderna (NASDAQ:MRNA) has agreed to pay US$950 million to resolve a long-running patent dispute tied to the technology used in its COVID-19 vaccine.The pharmaceuticals giant announced it has reached a global settlement with Arbutus Biopharma (NASDAQ:ABUS) and Genevant Sciences GmbH over claims... Keep Reading...
Scientists examining a sample under a microscope in a lab setting.

Gilead to Acquire Arcellx in US$7.8 Billion Bet on Cancer Therapy

Gilead Sciences (NASDAQ:GILD) announced plans to acquire cancer immunotherapy partner Arcellx (NASDAQ:ACLX) in a deal worth up to US$7.8 billion, moving to take full control of their jointly developed multiple myeloma therapy anito-cel as it seeks to expand its oncology pipeline.The agreement,... Keep Reading...

Interactive Chart

Latest Press Releases

Related News