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Individual Patient Expanded Access for Acellular Tissue Engineered Vessel (ATEV) for Vascular System Injuries

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Humacyte

Status

Conditions

Vascular System Injuries

Treatments

Biological: Acellular Tissue Engineered Vessel (ATEV) / Human Acellular Vessel (HAV)

Study type

Expanded Access

Funder types

Industry

Identifiers

NCT03631056
CLN-EA-IP

Details and patient eligibility

About

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

Full description

Procedure for Requesting Expanded Access:

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

General Criteria:

We will evaluate and respond to each expanded-access request that we receive 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:

If you contact Humacyte as described above, Humacyte anticipates that we will acknowledge receipt within ten (10) business days or less.

Sex

Volunteers

No Healthy Volunteers

Inclusion criteria

-

Exclusion criteria

-

Trial contacts and locations

0

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Central trial contact

Mauricio Berdugo, MD, MPH

Data sourced from clinicaltrials.gov

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