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Humacyte's Bioengineered Blood Vessel Outperforms the Standard of Care for Women on Dialysis in Phase 3 Results Presented at the Society for Vascular Surgery Vascular Annual Meeting

$HUMAPress releaseJun 15, 2026, 8:00 AM ETRead the release

Humacyte presented positive Phase 3 results from its V012 study, showing its bioengineered blood vessel (ATEV) outperformed the standard of care (AV fistula) for women on dialysis. Patients receiving ATEV remained catheter-free for an average of 220 days in the first year, compared to 129 days for those with AV fistulas, a statistically significant difference (p=0.00070). Infection rates were also significantly lower in the ATEV group (6 per 100 patient years vs. 23 for AV fistula).

Key figures

Drug Name
ATEV (acellular tissue engineered vessel)
Phase Of Trial
Phase 3
P value primary
0.0007
Infection rate avf
23 per 100 patient years
Infection rate atev
6 per 100 patient years
Six month patency avf
65.0%
Catheter free days avf
129
Six month patency atev
87.5%
Catheter free days atev
220

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