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Temporarily not availableNCT07141641Updated Sep 15, 2026

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

An expanded access record providing Acellular Tissue Engineered Vessel (ATEV) in Vascular Diseases and End Stage Renal Disease on Dialysis, sponsored by Humacyte, Inc.. Temporarily not available. Per ClinicalTrials.gov, last updated 2026-09-15.

Sponsored by Humacyte, Inc. · Expanded access

Study type
Expanded access
Access type
Individual patients
01

Study summary

Individual patient expanded access requests may be considered for patients who have no other treatment options and are not eligible for an ATEV clinical study.

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Procedure for Requesting Expanded Access:

The treating physician requesting expanded access must contact Humacyte directly with the basis for the request. Please include the Investigator's contact information so that Humacyte may follow up with the Investigator directly.

General Criteria:

The Humacyte Expanded Access Committee will evaluate and respond to each expanded-access request received on a case-by-case basis. Humacyte will consider the nature of the request, the patient's health, the available medical and scientific information about the investigational product, the balance of risk and potential benefit to the patient, the availability of investigational product, and the potential regulatory impact.

Anticipated Timing:

Humacyte will acknowledgement receipt of each Investigator request within ten (10) business days or less.

02

Conditions studied

  • Vascular Diseases
  • End Stage Renal Disease on Dialysis

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03

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)

Inclusion criteria

-

Exclusion criteria

Exclusion Criteria:

-

04

Access details

Study type
Expanded access
Access type
Individual patients

Available treatment

  • BiologicalAcellular Tissue Engineered Vessel (ATEV)
05

Where to request access

No study locations are listed for this record.

06

Registry details

Key details

Study ID
NCT07141641
Lead sponsor
Humacyte, Inc.
Responsible party
Sponsor
First posted
Aug 26, 2025
Last update
Sep 15, 2026
View the source record on ClinicalTrials.gov ↗

Requesting access

Expanded access is arranged between your doctor and the company. Ask your care team to contact the provider listed on this record.

No contact was published for this record. The registry link below has the sponsor’s details.

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Discussion

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