About Fragile X-associated primary ovarian insufficiency
Fragile X-associated primary ovarian insufficiency is a rare disease catalogued by Orphanet (ORPHA:642691). It is associated with the FMR1 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 Fragile X-associated primary ovarian insufficiency trials.
Search ClinicalTrials.gov for "Fragile X-associated primary ovarian insufficiency" or filter by Orphanet code ORPHA:642691 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 Fragile X-associated primary ovarian insufficiency trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Fragile X-associated primary ovarian insufficiency. Updated daily.