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Expanded Access Program for Autologous Muscle Derived Cells (AMDCs)

Expanded Access Program for Autologous Muscle Derived Cells (AMDCs)

Status
TEMPORARILY_NOT_AVAILABLE
Phases
Unknown
Study type
Expanded Access
Source
ClinicalTrials.gov
Registry ID
NCT04661293
Acronym
AMDC
Enrollment
Unknown
Registered
2020-12-10
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

This is an expanded access program (EAP) for eligible participants designed to provide access to autologous muscle derived cells (AMDCs). Treating physicians may submit requests for expanded access to Cook MyoSite's investigational product by email to MYO-ExpandedAccess@CookMyoSite.com.

Detailed description

Cook MyoSite, Inc. (Cook MyoSite) is committed to conducting rigorous, controlled clinical trials with variable inclusion and exclusion criteria based upon the indicated use under investigation. Participation in our clinical trials is the first and most preferable route to access our investigational product. We understand that there may be patients with a serious, life-threatening disease or condition that have explored all other treatment options and are unable or ineligible to participate in our clinical trials. Expanded access, otherwise known as "compassionate use" or "pre-approval access," is a potential pathway to access an investigational product that a patient may otherwise be unable to receive. Cook MyoSite will consider providing an investigational product to a qualified requesting physician currently licensed within the United States via the United States Food and Drug Administration's (FDA's) expanded access pathway outside of an active clinical trial when eligibility criteria are met.

Interventions

BIOLOGICALAutologous Muscle Derived Cells (AMDCs)

Sponsors

Cook MyoSite
Lead SponsorINDUSTRY

Eligibility

Inclusion criteria

Eligibility Criteria: 1. The patient has a serious or life-threatening disease or condition with no satisfactory alternative. 2. Positive assessment that the anticipated benefits outweigh the risks to the patient. 3. Positive assessment that Cook MyoSite has an adequate supply of resources for producing the investigational product. 4. A determination that expanded access will not interfere with Cook MyoSite's ability to complete clinical trials in a timely fashion or which might otherwise delay marketing approval and ultimately availability to all patients. 5. The patient can undergo a muscle biopsy procedure(s). 6. The patient can undergo Cook MyoSite's required donor screening and testing.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026