DiaMedica Therapeutics (DMAC) Corporate presentation summary
Event summary combining transcript, slides, and related documents.
Corporate presentation summary
8 Apr, 2026Market opportunity and unmet need
Preeclampsia and fetal growth restriction represent a $5B+ U.S. market with no approved disease-modifying therapies; acute ischemic stroke is a $10B+ U.S. market with significant unmet need, as ~80% of patients lack effective treatment options.
Lead program and mechanism of action
DM199 is a recombinant human KLK1 protein with a novel mechanism, producing all three major endothelial-derived vasodilators (NO, prostacyclin, EDHFs), improving blood flow and reducing blood pressure.
DM199 does not cross the placental barrier, supporting its safety profile in pregnancy.
Clinical development and results
Ongoing and planned phase 2/3 trials for preeclampsia, fetal growth restriction, and acute ischemic stroke, with interim phase 2 data showing significant blood pressure reduction and improved uterine artery perfusion.
DM199 demonstrated favorable safety and tolerability, with no serious treatment-emergent adverse events and no placental transfer detected.
In acute ischemic stroke, DM199 improved clinical outcomes in phase 2, offering a 24-hour treatment window and showing efficacy comparable to or better than tPA in relevant populations.
Latest events from DiaMedica Therapeutics
- Synthetic KLK1 therapy advances in pivotal trials for preeclampsia and stroke, with strong safety data.DMAC
Biotech Resurgence: Platforms and Pipelines of Today's Innovators16 Apr 2026 - Director elections, auditor ratification, and executive pay are up for vote at the 2026 AGM.DMAC
Proxy filing1 Apr 2026 - 2026 meeting seeks approval for director elections, auditor, executive pay, and expanded equity plan.DMAC
Proxy filing1 Apr 2026 - DM199 advanced in key trials with strong safety, efficacy, and a cash runway through 2H 2027.DMAC
Q4 202531 Mar 2026 - DM199 shows promise as a first-in-class therapy for preeclampsia and stroke, with strong clinical and financial backing.DMAC
Corporate presentation16 Mar 2026 - DM199 enters Phase II for preeclampsia, aiming for rapid, capital-efficient proof of concept.DMAC
Status Update3 Feb 2026 - R&D spending rose, $54.1M cash supports DM199 trials, cash runway extended to Q3 2026.DMAC
Q2 20242 Feb 2026 - Net loss rose to $16.5M as R&D for DM199 increased, with cash runway through Q3 2026.DMAC
Q3 202414 Jan 2026 - Clinical trials advanced, net loss $24.4M, and cash runway extends into Q3 2026.DMAC
Q4 202426 Dec 2025