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acellular tissue engineered vessel

acellular tissue engineered vessel: 5 clinical trials tracked.

acellular tissue engineered vessel evidence translation

What we can confirm

5 tracked trials

No verified listed company relationship

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about acellular tissue engineered vessel, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence3 indications · 1 study sponsors
Clinical Trial Registry Records (5)

Individual Patient Expanded Access for Acellular Tissue Engineered Vessel (ATEV) for Vascular Disease and Dialysis Access

NCT07141641Registry updated 2026-09-15·HUMA
Temporarily not available
Expanded AccessHumacyte, Inc.

A Prospective, Multi-center, Open-label Study, to Assess the Safety and Efficacy of SYMVESS® as a Vascular Conduit in Adolescents With Extremity Arterial Injury When Autologous Vein Graft is Not Feasible.

NCT07762313Registry updated 2026-08-13·Phase 3·HUMA
Not yet recruiting

Primary endpoint: Number of Participants with Treatment-Related Adverse Events

Interventionalopen10 targetStarted 2026-09Completion 2028-12Humacyte, Inc.

A Phase 4 Observational Multicenter Study to Evaluate the Safety and Efficacy of SYMVESS™ in a Real World Setting for Arterial Replacement or Reconstruction in Patients With Extremity Vascular Trauma

NCT07762794Registry updated 2026-08-13·Phase 4·HUMA
Not yet recruiting

Primary endpoint: Kaplan-Meier estimated Symvess secondary patency

Interventionalopen125 targetStarted 2026-09Completion 2030-09Humacyte, Inc.

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

NCT05908084Registry updated 2026-06-26·Phase 3·HUMA
Active, not recruiting

Primary endpoint: The number of catheter-free days since randomization to Month 12.

InterventionalRandomizedsingle121 targetStarted 2023-09Completion 2028-0632 sites · United StatesHumacyte, Inc.

A Phase 2/3 Study for the Evaluation of Safety and Efficacy of Humacyte's ATEV for Vascular Replacement or Reconstruction in Patients With Life or Limb-threatening Vascular Trauma

NCT03005418Registry updated 2026-07-29·Phase 2/Phase 3·HUMA
Completed

Primary endpoint: Primary Patency Rate of the Human Acellular Vessel (HAV) at Day 30 in the All HAV Group

Interventionalopen72 enrolledStarted 2018-09Completion 2026-0529 sites · Israel, United StatesHumacyte, Inc.