DiaMedica <a href="https://laohu8.com/S/LENZ">Therapeutics</a> Advances DM199 Preeclampsia Clinical Program Following FDA Meeting
DiaMedica Therapeutics Inc. has announced the completion of a pre-Investigational New Drug $(IND)$ meeting with the U.S. Food and Drug Administration (FDA) regarding a planned study of DM199 for preeclampsia. The FDA requested an additional non-clinical, 10-day modified embryo-fetal development and pre- and postnatal development study in a rabbit model, with results expected by the second quarter of 2026. Additionally, an ongoing Phase 2 investigator-sponsored trial of DM199 in South Africa has dosed over 30 women with late-stage preeclampsia. Interim data from this trial have shown statistically significant reductions in blood pressure and dilation of intrauterine arteries, with no placental transfer of DM199 observed. The full results of the rabbit study are anticipated in the future.
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 via Business Wire (Ref. ID: 20251218113728) on December 18, 2025, and is solely responsible for the information contained therein.
免責聲明：投資有風險，本文並非投資建議，以上內容不應被視為任何金融產品的購買或出售要約、建議或邀請，作者或其他用戶的任何相關討論、評論或帖子也不應被視為此類內容。本文僅供一般參考，不考慮您的個人投資目標、財務狀況或需求。TTM對信息的準確性和完整性不承擔任何責任或保證，投資者應自行研究並在投資前尋求專業建議。