Clin2
NCT05715957Possibly a fitEnrolling by invitation

Follow-up study for women who carry a DMD gene change

Muscular DystrophyDuchenne Muscular DystrophyBecker Muscular Dystrophy

Part of Bones, joints & muscles, Brain & nervous system, Genetic & congenital clinical trials.

This study follows women who have a confirmed DMD gene mutation (a genetic change related to Duchenne/Becker muscular dystrophy) to learn more about health and muscle-related measurements. Depending on the part of the study, you may be asked to take part in MRI or other assessments.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
103 people
Ages
18 years and older
Study type
Observational

Who can take part

  • You are a woman who is at least 18 years old
  • You have genetic test results showing you carry a DMD gene mutation
  • For Part 1 only: you also joined this study about 6 years ago
  • You can follow any study rules about stopping certain medicines if needed
  • You can take part in the planned measurements, including MRI if you are eligible

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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