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DiaMedica Therapeutics Inc
NASDAQ:DMAC

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DiaMedica Therapeutics Inc
NASDAQ:DMAC
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Price: 5.65 USD 3.48% Market Closed
Market Cap: $304.4m

DiaMedica Therapeutics Inc
Investor Relations

DiaMedica Therapeutics is a clinical-stage drug developer focused on treatments for serious vascular and kidney-related diseases. Its main program is a drug called DM199, a lab-made version of a natural human protein, which the company is testing for conditions such as acute ischemic stroke and preeclampsia. It does not run a drugstore or sell medicines to patients today; it is trying to turn its research into approved treatments that doctors and hospitals could use. The company’s customers, if its drugs succeed, would be hospitals, physicians, and health systems that treat acute and high-risk medical conditions. For now, DiaMedica makes money in the way most early biotech companies do: it raises capital to fund research, clinical trials, and regulatory work, and it may also use partnerships or licensing deals if it finds larger drug makers to help develop or commercialize its programs. What makes its business different is that it is built around a single scientific platform rather than a broad portfolio of products. That means the company’s value depends heavily on whether its lead drug shows clear clinical benefit and can win regulatory approval. In biotech, that kind of focused model can create large upside, but it also carries a high level of scientific and development risk.

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Last Earnings Call
Fiscal Period
Q1 2026
Call Date
May 7, 2026
AI Summary
Q1 2026

Clinical progress: DiaMedica said it made solid progress across both its preeclampsia and stroke programs and expects multiple clinical milestones through the end of 2027.

Preeclampsia update: The company expects a data update later this quarter from the late-onset preeclampsia extension cohort, and said the next two cohorts should start this summer.

Stroke milestone: ReMEDy2 enrollment has surpassed 70% of the target needed for the interim analysis, which management still expects to complete by the end of 2026.

FDA path: The U.S. early-onset preeclampsia program remains paused on additional nonclinical work, but Canada has already approved the study and the U.K. filing is expected this quarter.

Cash runway: DiaMedica ended the quarter with $51.3 million in cash and investments and said that should fund planned clinical studies and operations through 2027.

Key Financials
Cash, cash equivalents and short-term investments
$51.3 million
Current liabilities
$5.7 million
Working capital
$46.6 million
Net cash used in operating activities
$9.1 million
Research and development expense
$8.0 million
General and administrative expense
$2.5 million
ReMEDy2 enrollment
over 70%
Stroke resample size
between 300 and 700 patients
Late-onset preeclampsia extension cohort
12 additional patients
Part 1b and Part 2 doses
5, 10 and 15 micrograms per kg
Canadian sites for early-onset preeclampsia study
2 sites
Activated sites
approximately 70 sites
Earnings Call Recording
Other Earnings Calls

Management

Mr. Dietrich John Pauls MBA
President, CEO & Director
No Bio Available
Mr. Scott Kellen CPA
CFO & Corporate Secretary
No Bio Available
Dr. Ambarish Shah Ph.D.
Chief Technology Officer
No Bio Available
Mr. Dominic R. Cundari
Chief Commercial Officer
No Bio Available
Mr. David J. Wambeke
Chief Business Officer
No Bio Available
Dr. Lorianne K. Masuoka M.D.
Chief Medical Officer
No Bio Available

Contacts

Address
MINNESOTA
Minneapolis
Two Carlson Parkway, Suite 260
Contacts
+17634965454.0
www.diamedica.com
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