Progress in Preeclampsia Program
DiaMedica obtained ethics approval and began dosing preeclamptic mothers in their DM199 study, marking the first study of DM199 in a pregnancy-related condition. This highlights DM199's potential as a treatment for preeclampsia, a condition with no FDA-approved treatments.
Expansion of Stroke Program
Activated 30 clinical sites for the stroke study, with plans to expand globally. The study protocol has been updated to include more patient populations, potentially increasing enrollment.
Strong Financial Position
DiaMedica reported a total combined cash and investments of $44.1 million, providing a financial runway into Q3 of 2026.
Positive Safety Review
The Data Safety Monitoring Board completed a comprehensive safety review, finding no significant safety concerns, allowing the ReMEDy2 trial to continue without modification.