Profusa U.S. Study Met Primary End Points as Presented at Late Breaking Clinical Trials at Paris Vascular Insights 2025
Profusa, Inc. (PFSA)
Company Research
Source: GlobeNewswire
Data from FDA-advised study demonstrates Lumee™ Oxygen tissue monitoring is a safe and effective long-term method in PAD patients and will support potential FDA submission; strongly correlates with transcutaneous partial pressure of oxygen BERKELEY, Calif, Dec. 15, 2025 (GLOBE NEWSWIRE) -- Profusa, Inc. (“Profusa” or the “Company”) (Nasdaq: PFSA), a commercial stage digital health company pioneering a next-generation technology platform enabling the continuous monitoring of an individual’s biochemistry, presented pilot phase data demonstrating the study’s primary end points were successfully met at the late breaking clinical trial session at the Paris Vascular Insights (PVI) 2025, on December 13, 2025, in Paris, France. Data from the FDA-advised clinical study performed in the U.S. (University of California San Francisco, San Francisco VA Medical Center, and San Francisco General Hospital) showed Lumee oxygen tissue monitoring is a safe and effective method for long term monito
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- Profusa U.S. Study Met Primary End Points as Presented at Late Breaking Clinical Trials at Paris Vascular Insights 2025 [Yahoo! Finance]Yahoo! Finance
- Profusa to Present US-Study Clinical Data at Leipzig Interventional Course (LINC) 2026 [Yahoo! Finance]Yahoo! Finance
- Profusa to Present US-Study Clinical Data at Leipzig Interventional Course (LINC) 2026GlobeNewswire
- Profusa to Present Late Breaking U.S.-Based Clinical Trial Update at Paris Vascular Insights 2025GlobeNewswire
- Profusa (NASDAQ:PFSA) is now covered by analysts at <a style="font-weight:bold" href="https://weissratings.com/">Weiss Ratings</a>. They set a "sell (e+)" rating on the stock.MarketBeat