Clin2
NCT06066580Possibly a fitEnrolling by invitation

Long-term safety study of sevasemten for Becker muscular dystrophy

Becker Muscular Dystrophy

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

This study continues treatment with the investigational drug sevasemten for people with Becker muscular dystrophy who have already been in a previous sevasemten study. The goal is to learn more about the drug's safety and how well it works over a longer period.

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

Phase
Phase 2
Enrollment
260 people
Ages
Any age
Study type
Interventional

Who can take part

  • You must be male and have a diagnosis of Becker muscular dystrophy.
  • You must have completed a prior sevasemten study (ARCH, CANYON, GRAND CANYON, or DUNE) within the last few months.
  • You must have finished all required visits in that prior study.
  • You must not be taking strong or moderate CYP3A4 inhibitors or inducers (medications that affect how the body processes drugs).
  • You must not have taken any other investigational drug (besides sevasemten) in the last 30 days or 5 half-lives, whichever is longer.
  • You must not have taken oral corticosteroids for Becker muscular dystrophy in the last 6 months.

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.

Similar studies

Other trials that look related to this one.

NCT07740057Not yet recruiting
Understanding brain and muscle changes in Becker muscular dystrophy

This study looks at how Becker muscular dystrophy affects the brain and muscles using imaging, thinking tests, and muscle function checks. It aims to learn more about the condition to improve care.

Paris
NCT05715957Enrolling by invitation
Follow-up study for women who carry a DMD gene change

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.

Copenhagen
NCT06606340Enrolling by invitation
Long-term study of eteplirsen, golodirsen, or casimersen for DMD

This study follows people with Duchenne muscular dystrophy (DMD) who are taking eteplirsen, golodirsen, or casimersen. It aims to understand how these medicines work in everyday life over a long period.

Little Rock, Arkansas
NCT05967351Enrolling by invitation· Phase 3
Long-term follow-up for Duchenne patients treated before

This study checks how people with Duchenne muscular dystrophy are doing long-term after receiving delandistrogene moxeparvovec (SRP-9001) in an earlier trial. It helps researchers understand the long-term safety and effects of that treatment.

Little Rock, Arkansas
NCT06867107Enrolling by invitation· Phase 2
Long-term follow-up study of SAT-3247 for Duchenne muscular dystrophy

This study follows people with Duchenne muscular dystrophy who were in an earlier SAT-3247 trial, or who meet certain other criteria, to see how the medicine works over a longer time. It aims to gather more safety and effectiveness information.

Los Angeles, California
NCT07573631Enrolling by invitation· Phase 2
Long-term Safety Study of BMN 351 for Duchenne Muscular Dystrophy

This study continues treatment with an investigational medicine called BMN 351 for people with Duchenne muscular dystrophy (a genetic muscle-weakening condition). It checks whether the medicine remains safe and effective when used over a longer period, building on results from an earlier trial.

Milan, Italy

Hear when a new Becker Muscular Dystrophy trial opens

We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.