- DiaMedica annual report for fiscal year 2025 highlighted continued development of lead candidate DM199 across preeclampsia and acute ischemic stroke programs.
- Health Canada issued a “No Objection” letter enabling a DiaMedica-sponsored Phase 2 dose-ranging study in early-onset preeclampsia.
- ReMEDy2 Phase 2/3 pivotal trial in acute ischemic stroke reported improving site activation and enrollment following protocol refinements.
- Board expansion added Dan O’Connor, citing experience from Ambryx Biopharma acquisition by Johnson & Johnson in 2024.
- Operating runway guidance reaffirmed through end of 2027, supporting current development plan.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. DiaMedica Therapeutics Inc. published the original content used to generate this news brief on April 01, 2026, and is solely responsible for the information contained therein.
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