Progressive muscular dystrophy
MONDO:0016106Also known as: progressive muscular dystrophy
129 clinical trials for this condition and its sub-types, 2 tagged with Progressive muscular dystrophy itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Part of
Sub-types of Progressive muscular dystrophy
-
Myotonic dystrophy 56 trials · 57 incl. sub-types
8 sub-types
- Myotonic dystrophy type 1 45 trials Sub-types →
- Myotonic dystrophy type 2 11 trials
- Congenital myotonic dystrophy 9 trials
- Childhood-onset Steinert myotonic dystrophy 2 trials
- Juvenile-onset Steinert myotonic dystrophy 2 trials
- Adult-onset Steinert myotonic dystrophy 0 trials
- Late-onset Steinert myotonic dystrophy 0 trials
- Myotonic cataract 0 trials
-
Facioscapulohumeral muscular dystrophy 36 trials · 40 incl. sub-types
5 sub-types
-
Limb-girdle muscular dystrophy 17 trials · 26 incl. sub-types
3 sub-types
- Autosomal recessive limb-girdle muscular dystrophy 0 trials · 18 incl. sub-types Sub-types →
- Muscular dystrophy, limb-girdle, autosomal dominant 0 trials · 4 incl. sub-types Sub-types →
- POMGNT2-related limb-girdle muscular dystrophy R24 1 trial
-
Oculopharyngeal muscular dystrophy 3 trials
2 sub-types
- Oculopharyngeal muscular dystrophy 1 0 trials
- Oculopharyngeal muscular dystrophy 2 0 trials
-
Emery-Dreifuss muscular dystrophy 1 trial · 3 incl. sub-types
4 sub-types
- Autosomal dominant Emery-Dreifuss muscular dystrophy 0 trials · 3 incl. sub-types Sub-types →
- Emery-Dreifuss muscular dystrophy 3, autosomal recessive 0 trials
- X-linked Emery-Dreifuss muscular dystrophy 0 trials Sub-types →
- Scapuloperoneal myopathy 0 trials Sub-types →
-
8 sub-types
- Tukel syndrome 0 trials
- Congenital fibrosis of extraocular muscles type 1 0 trials
- Fibrosis of extraocular muscles, congenital, 2 0 trials
- Fibrosis of extraocular muscles, congenital, 3A, with or without extraocular involvement 0 trials
- Fibrosis of extraocular muscles, congenital, 3b 0 trials
- Fibrosis of extraocular muscles, congenital, 3c 0 trials
- Fibrosis of extraocular muscles, congenital, 5 0 trials
- Fibrosis of extraocular muscles, congenital, with synergistic divergence 0 trials
-
Bethlem myopathy 0 trials
4 sub-types
- Bethlem myopathy 1A 0 trials
- Bethlem myopathy 1B 0 trials
- Bethlem myopathy 1C 0 trials
- Bethlem myopathy 2 0 trials
-
1 sub-type
-
Oculopharyngodistal myopathy 0 trials
5 sub-types
- Oculopharyngodistal myopathy 1 0 trials
- Oculopharyngodistal myopathy 2 0 trials
- Oculopharyngodistal myopathy 3 0 trials
- Oculopharyngodistal myopathy 4 0 trials
- Oculopharyngodistal myopathy 5 0 trials
Most studied deeper sub-types
-
Can an experimental infusion slow muscle loss in FSHD?
Disease control Not yet recruitingThis trial tests an experimental drug called SFL-0821 in adults with facioscapulohumeral muscular dystrophy (FSHD), a genetic condition that causes progressive muscle weakness. Researchers give the drug by intravenous infusion, either once or multiple times, and compare it agains…
Phase 1/2 • Sponsor: Soufflé Therapeutics, Inc. • Aim: Disease control
Last updated Sep 20, 2026 00:00 UTC
-
Could a common blood pressure pill ease muscle stiffness? early trial launches
Symptom relief Not yet recruitingThis early-stage trial tests amlodipine, a calcium channel blocker used for high blood pressure, in 20 adults with myotonic dystrophy type 1. The goal is to see if the drug is safe and can improve muscle strength, reduce stiffness, and help with daily function. All participants w…
Phase 1 • Sponsor: University of Rochester • Aim: Symptom relief
Last updated Jun 27, 2026 08:03 UTC
-
Can watching the course of myotonic dystrophy unlock better care?
Knowledge-focused Not yet recruitingThis study follows 100 adults with myotonic dystrophy (types 1 or 2) for two years to understand how muscle stiffness, daily function, and heart health change over time. Researchers will look back at up to 18 months of past medical records and then track participants with clinic …
Sponsor: Lupin Ltd. • Aim: Knowledge-focused
Last updated Jul 30, 2026 00:00 UTC
-
New registry aims to improve care for muscular dystrophy patients
Knowledge-focused Not yet recruitingThis study is creating a registry for people with Duchenne and Becker muscular dystrophy, as well as symptomatic female carriers. The goal is to collect health data and quality-of-life information to monitor how new therapies work in real-world settings. Up to 1,500 participants …
Sponsor: Dr. Andreas Ziegler • Aim: Knowledge-focused
Last updated Jun 27, 2026 09:05 UTC