Clin2
NCT03373968Possibly a fitRecruiting

Long-term study of givinostat safety in Duchenne muscular dystrophy

Duchenne Muscular Dystrophy

Treatments studied

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

This trial looks at how safely givinostat works over a longer time in people with Duchenne muscular dystrophy (DMD). It mainly checks long-term side effects and tolerability, especially in a specific subgroup of muscle fat levels.

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

Phase
Phase 2/Phase 3
Enrollment
206 people
Ages
7 years and older
Study type
Interventional

Who can take part

  • You are at least 6 years old
  • You previously joined a givinostat DMD study and either finished it or were screened into a specific off-target muscle group
  • Your muscle fat level in a specific thigh muscle (VL) is very low (≤5%) or high (>30%) based on a special scan
  • Your parent/guardian (and you, if applicable) can sign consent, and you can agree to the study steps
  • You (or a partner, if applicable) must use acceptable contraception from the prior study through 3 months after the last dose
  • Recent treatments must follow the rules: no other medicines that could affect muscle strength in the last 3 months (vitamin D/calcium are allowed)

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.

NCT06769633Recruiting· Phase 2
Study of givinostat in young boys with Duchenne muscular dystrophy

This trial tests an experimental drug called givinostat in boys ages 2 to under 6 years with Duchenne muscular dystrophy (DMD). The study looks at how the drug works in the body and if it is safe, with the goal of finding new treatment options for young children.

Brussels
NCT05933057Recruiting· Phase 3
Givinostat for wheelchair-bound boys with Duchenne muscular dystrophy

This Phase 3 trial tests givinostat to see if it can improve safety and functional outcomes in boys with Duchenne muscular dystrophy who cannot walk. You might be a candidate if you meet age, genetic diagnosis, wheelchair-level mobility, and specific arm-strength/respiratory/heart criteria.

Leuven
NCT03882827Recruiting
Natural history study of Duchenne muscular dystrophy in young boys

This study follows boys with Duchenne muscular dystrophy over time to better understand how the condition changes and how standard treatments affect health and function. It does not appear to test a new medicine, but it may help doctors plan better future care and studies.

Brussels
NCT07209332Enrolling by invitation· Phase 2
Long-term safety study of WVE-N531 for Duchenne muscular dystrophy

This trial is for people who have already taken WVE-N531 in an earlier study. It continues to check the medicine's safety and effects over a longer period.

Amman
NCT06564974Recruiting
Long-term safety study of Agamree for Duchenne muscular dystrophy

This study watches boys with Duchenne muscular dystrophy who are already taking Agamree (vamorolone) to see how safe it is over a long period. It helps doctors understand the medicine's effects over time.

Phoenix, Arizona
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

Hear when a new Duchenne Muscular Dystrophy trial opens

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