Disease Directory Primary mediastinal large B-cell lymphoma
Blood

Primary mediastinal large B-cell lymphoma

Type

Disease

Gene

BCL6, XPO1

About Primary mediastinal large B-cell lymphoma

Primary mediastinal large B-cell lymphoma is a rare disease catalogued by Orphanet (ORPHA:98838). It is associated with the BCL6, XPO1 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 Primary mediastinal large B-cell lymphoma trials.

Search ClinicalTrials.gov for "Primary mediastinal large B-cell lymphoma" or filter by Orphanet code ORPHA:98838 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:98838)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Primary mediastinal large B-cell lymphoma trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Primary mediastinal large B-cell lymphoma. Updated daily.