About Proximal spinal muscular atrophy type 1
Proximal spinal muscular atrophy type 1 is a rare disease catalogued by Orphanet (ORPHA:83330). It is associated with the SMN2, NAIP, SMN1 genes. Search below for active recruiting clinical trials from ClinicalTrials.gov, or visit the Orphanet expert page for specialist centres, natural history studies, and patient registries.
Clinical Trial Eligibility Tips
What to know before applying to Proximal spinal muscular atrophy type 1 trials.
Search ClinicalTrials.gov for "Proximal spinal muscular atrophy type 1" or filter by Orphanet code ORPHA:83330 to find disease-specific studies.
Ask your specialist to refer you to a Centre of Expertise — Orphanet lists all accredited centres for this condition worldwide.
Natural history studies and patient registries often enrol before drug trials open — contact the Orphanet patient community first.
Patient Resources
Find recruiting Proximal spinal muscular atrophy type 1 trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Proximal spinal muscular atrophy type 1. Updated daily.