Why it may matterVerify against the original reporting
Positive Phase 2 DM199 topline in preeclampsia, first FGR cohort enrollment, and regulatory progress (Canada) combine with a clear cash runway to support near-term upside, despite ongoing losses and development risk typical of clinical-stage biotechs.
AI summary
What happened, with direct paths to the underlying reporting
DiaMedica reports encouraging Phase 2 DM199 data in preeclampsia and completes enrollment for the first fetal growth restriction cohort, with a September KOL call planned. The AIS interim readout is slated for early 2027, while Health Canada has approved a Phase 2 PE study with first patient in Q4 2026, supported by a cash runway through 2027.
Enrollment of first FGR cohort completed; KOL call scheduled for September.
Phase 2 PE Part 1a topline: SBP down 29.1 mmHg, DBP down 17.0; SBP <160 for 24h.
AIS ReMEDy2 interim analysis expected early 2027; ~70 sites across US/Canada/UK/Europe.
$43.5M cash and investments as of 6/30/2026; runway through 2027.
Health Canada authorizes global Phase 2 PE study; first patient due in Q4 2026.
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