Disease Directory Solitary fibrous tumor
Rare Disease

Solitary fibrous tumor

Type

Disease

Gene

STAT6, NAB2

About Solitary fibrous tumor

Solitary fibrous tumor is a rare disease catalogued by Orphanet (ORPHA:2126). It is associated with the STAT6, NAB2 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 Solitary fibrous tumor trials.

Search ClinicalTrials.gov for "Solitary fibrous tumor" or filter by Orphanet code ORPHA:2126 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:2126)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Solitary fibrous tumor trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Solitary fibrous tumor. Updated daily.