Phase 1 Muscular Dystrophy Trial, Recruiting NCT06692426 Sponsor: Masonic Cancer Center, University of Minnesota Condition: Muscular Dystrophy
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Phase 1 Muscular Dystrophy Trial, Recruiting

NCT06692426
Recruiting Phase 1

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You have been diagnosed with Duchenne muscular dystrophy (DMD), confirmed by a genetic test showing a mutation in the DMD gene and/or a muscle biopsy showing no dystrophin protein
  • You are not able to walk (non-ambulatory)
  • You have a specific small muscle in both feet (called the extensor digitorum brevis) that is still working (confirm with trial site)
  • You have not taken any experimental treatments for more than 30 days before joining
  • You are 18 years old or older at the time of signing consent
  • Your organs (such as kidneys, liver, heart, and lungs) are working well enough, confirmed by blood and other tests done within a recent timeframe before enrolling
  • If you have a partner who could become pregnant, you must be willing to use at least two forms of birth control (one must be a barrier method, such as a condom) during the study and for 3 months after stopping one of the study medications (tacrolimus)
  • You are able to understand and follow instructions well enough to complete the required tasks during the study
  • You are willing to be monitored for up to 15 years, as required for studies involving genetically modified cells
  • You are willing to give your written consent to participate in the study voluntarily

Who may not be able to join:

  • You have certain antibodies in your blood that react against the transplant product used in this trial (called MyoPAXon) (confirm with trial site)
  • You are currently receiving another experimental treatment
  • You have a known allergy to any ingredients in MyoPAXon

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
Phase 1: approximately ~10% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Phone: 612-624-9452

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 1
Sponsor
Masonic Cancer Center, University of Minnesota
Registry
ClinicalTrials.gov
Start date
20 March 2025
Est. completion
3 March 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Maximal tolerable dose (MTD) of MyoPAXon

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov