Disease Directory Pituitary gigantism
Endocrine

Pituitary gigantism

Type

Disease

Gene

AIP, MEN1

About Pituitary gigantism

Pituitary gigantism is a rare disease catalogued by Orphanet (ORPHA:99725). It is associated with the AIP, MEN1 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 Pituitary gigantism trials.

Search ClinicalTrials.gov for "Pituitary gigantism" or filter by Orphanet code ORPHA:99725 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:99725)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Pituitary gigantism trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Pituitary gigantism. Updated daily.