Humacyte ((HUMA)) announced an update on their ongoing clinical study.
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Humacyte (HUMA) has initiated a Phase 3 clinical trial titled A Phase 3 Randomized Study to Compare the Efficacy and Safety of the Humacyte Acellular Tissue Engineered Vessel (ATEV) With That of an Autogenous Arteriovenous Fistula (AVF) in Female Patients With End-Stage Renal Disease Requiring Hemodialysis. The study aims to evaluate the number of catheter-free days and the rate and severity of dialysis access-related infections between the ATEV and AVF groups over a 12-month period, focusing on female patients with end-stage renal disease (ESRD) requiring hemodialysis.
The intervention being tested is the Acellular Tissue Engineered Vessel (ATEV), a biological implant designed to serve as an arterio-venous access point for hemodialysis. It is compared against the traditional autogenous arteriovenous fistula (AVF) procedure.
This interventional study employs a randomized, parallel assignment model with single masking. The primary purpose is treatment, with participants allocated to either the ATEV or AVF treatment arms. Masking is applied to outcomes assessors to ensure unbiased result evaluation.
The study began on April 28, 2023, and is currently recruiting participants. The primary completion date is anticipated to be in March 2025, with the last update submitted on March 13, 2025. These dates are crucial for tracking the study’s progress and potential market entry timelines.
Humacyte’s clinical update could significantly impact its stock performance and investor sentiment, especially if the ATEV proves to be a safer and more effective alternative to AVF. This development positions Humacyte competitively within the renal treatment market, potentially influencing industry dynamics.
The study is ongoing, with further details available on the ClinicalTrials portal.