Disease Directory Cystic fibrosis
Rare Disease

Cystic fibrosis

Type

Disease

Gene

SERPINA1, SLC26A9, SLC6A14, SLC9A3, CEACAM3, CEACAM6

About Cystic fibrosis

Cystic fibrosis is a rare disease catalogued by Orphanet (ORPHA:586). It is associated with the SERPINA1, SLC26A9, SLC6A14 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 Cystic fibrosis trials.

Search ClinicalTrials.gov for "Cystic fibrosis" or filter by Orphanet code ORPHA:586 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

Patient Organization

Orphanet

Visit website ↗

Orphanet

European reference resource for rare diseases (ORPHA:586)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Cystic fibrosis trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Cystic fibrosis. Updated daily.