Disease Directory NUT midline carcinoma
Oncology

NUT midline carcinoma

Type

Disease

Gene

NUTM1, BRD4

About NUT midline carcinoma

NUT midline carcinoma is a rare disease catalogued by Orphanet (ORPHA:443167). It is associated with the NUTM1, BRD4 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 NUT midline carcinoma trials.

Search ClinicalTrials.gov for "NUT midline carcinoma" or filter by Orphanet code ORPHA:443167 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:443167)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting NUT midline carcinoma trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for NUT midline carcinoma. Updated daily.