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DiaMedica Receives FDA Feedback on DM199 Preeclampsia Nonclinical Program

$DMACPress releaseJun 16, 2026, 8:30 AM ETRead the release

DiaMedica received FDA feedback requesting additional nonclinical reproductive toxicity data for DM199 to support a U.S. IND for preeclampsia treatment. The company believes it can leverage previous rat study data by initiating a new pharmacokinetic and activity study to demonstrate sufficient exposure and enzymatic effect.

Key figures

Drug Name
DM199 (rinvecalinase alfa)

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