Humacyte Reports Positive Two-Year Results for Bioengineered Vessel in Dialysis Access Trial

Reuters11-10

Humacyte Reports Positive Two-Year Results for Bioengineered Vessel in Dialysis Access Trial

Humacyte Inc. announced the presentation of positive two-year results from the V007 Phase 3 clinical trial evaluating its acellular tissue engineered vessel (ATEV) for arteriovenous (AV) access in hemodialysis patients. The data, which were presented at the American Society of Nephrology's Kidney Week 2025, indicated that the ATEV demonstrated a superior duration of use over 24 months compared to autogenous fistula in high-need patient subgroups, including female, obese, and diabetic individuals, who typically experience poorer outcomes with AV fistula procedures. The ATEV is currently investigational for uses other than extremity vascular trauma and has not received FDA approval for other indications.

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. Humacyte Inc. published the original content used to generate this news brief on November 10, 2025, and is solely responsible for the information contained therein.

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