Rare condition
Progressive muscular atrophy
76
studies recruiting now
as of 7 Sept 2026
393
studies registered in total
as of 7 Sept 2026
8
countries with a recruiting site
as of 7 Sept 2026
23 Jul 2026
most recent study posted
among recruiting studies
Recruiting trials
A Study Evaluating the Effectiveness and Safety of Risdiplam Administered as an Early Intervention in Pediatric Participants With Spinal Muscular Atrophy After Gene Therapy
A Study of Risdiplam in Participants With Type I and Type II Spinal Muscle Atrophy (SMA)
A Study to Find Out How Nusinersen is Processed in the Body When Given Through the ThecaFlex DRx™ System in Adult and Pediatric Participants With Spinal Muscular Atrophy (PIERRE-PK)
Interfacing With NeuroTechnology to Expand Neural Throughput (INTENT)
Showing the 5 most recently updated recruiting studies, as recorded 7 Sept 2026. Live status on each study page.
See all 76 recruiting studiesWhere recruiting studies are running
Countries with at least one recruiting site among the studies above, 7 Sept 2026. Tap a country to search trials there.
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Patient organisations
We do not yet list a dedicated organisation for this condition. The directories below are the best route.
About Progressive muscular atrophy
RareTrial does not yet hold a plain-language description of this condition. The most reliable starting point is Orphanet’s expert page, which lists specialist centres, registries and patient organisations.
Treatments being studied
6 approved treatments and 12 in clinical development, from Open Targets (CC BY 4.0). Not medical advice.
+ 4 more in development
Related conditions
Information, not medical advice. Trial listings are shown as recorded on ClinicalTrials.gov; whether any study is right for you is a decision for you and your clinicians, and eligibility is decided by each research team. Disease information from Orphanet (CC BY 4.0).