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Humacyte Acellular Tissue Engineered Vessel (ATEV) in Patients With Vascular Trauma

Completed · Phase 2, Phase 3 · NCT03005418

Conditions: Trauma, Vascular System Injury

At a glance

Research payments reported, 2025
$111,631
U.S. investigators named
12
Sites paid
12
Planned or actual enrollment
72

About the trial

Sponsor
Humacyte, Inc. (with Atlantic Research Group, U.S. Army Medical Research and Development Command)
Tested
Acellular Tissue Engineered Vessel (ATEV) (biological)
Dates
Started 2018-09-01; completion 2026-05-15
Results posted
Yes

This study evaluates the use of the Acellular Tissue Engineered Vessel (ATEV) in adults with vascular trauma below the neck who are undergoing vascular reconstructive surgery. There will be an extremity cohort and an torso cohort. All subjects will be implanted with an ATEV as an interposition vessel or bypass using standard vascular surgical techniques. There is no control arm.

From ClinicalTrials.gov, last updated 2026-07-29. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Humacyte Global, Inc. reported $111,631 in research payments for this study in 2025 (16 payments).

Products named: Symvess

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.