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Clinical trial

Frequency and Clinical Phenotype of BAP1 Hereditary Predisposition Syndrome

NCT04792463 is registered in ClinicalTrials.gov with Mohamed Abdel-Rahman as lead sponsor.

NCT NCT04792463
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Registry record

As filed in ClinicalTrials.gov.

Title
Frequency and Clinical Phenotype of BAP1 Hereditary Predisposition Syndrome
Lead sponsor
Mohamed Abdel-Rahman
Phase
Observational
Overall status
Recruiting
Start date
March 3, 2015
Completion date
July 1, 2026
Enrollment
500 (estimated)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

bap1 gene mutation, cholangiocarcinoma, cutaneous melanoma, hepatocellular carcinoma, meningioma atypical, mesothelioma, renal cell carcinoma, uveal melanoma