Profusa Reports Positive US Clinical Trial Results for Lumee Sensor in PAD Patients

Reuters
Jan 29
Profusa Reports Positive US Clinical Trial Results for Lumee Sensor in PAD Patients

Profusa Inc. has announced positive results from a US-based clinical study evaluating the Lumee™ sensor in patients with peripheral artery disease (PAD). The results, which were presented at the Leipzig Interventional Course $(LINC)$ 2026, showed that the sensors remained functional for up to one year and no sensor placement related adverse events were reported. The company expects to begin commercial activities in the European Union with Lumee oxygen revenue projected to commence in the second quarter of 2026, and estimates potential revenue of $0.5 to $2 million in 2026 and $9 to $13 million in 2027.

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. Profusa Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9644911-en) on January 29, 2026, and is solely responsible for the information contained therein.

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