About Familial spontaneous pneumothorax
Familial spontaneous pneumothorax is a rare disease catalogued by Orphanet (ORPHA:2903). It is associated with the FLCN gene. 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 Familial spontaneous pneumothorax trials.
Search ClinicalTrials.gov for "Familial spontaneous pneumothorax" or filter by Orphanet code ORPHA:2903 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 Familial spontaneous pneumothorax trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Familial spontaneous pneumothorax. Updated daily.