Disease Directory Squamous cell carcinoma of the oropharynx
Oncology

Squamous cell carcinoma of the oropharynx

Type

Disease

Gene

TNFRSF10B, PTEN, ING1

About Squamous cell carcinoma of the oropharynx

Squamous cell carcinoma of the oropharynx is a rare disease catalogued by Orphanet (ORPHA:500478). It is associated with the TNFRSF10B, PTEN, ING1 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 Squamous cell carcinoma of the oropharynx trials.

Search ClinicalTrials.gov for "Squamous cell carcinoma of the oropharynx" or filter by Orphanet code ORPHA:500478 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

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Orphanet

European reference resource for rare diseases (ORPHA:500478)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Squamous cell carcinoma of the oropharynx trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Squamous cell carcinoma of the oropharynx. Updated daily.