# Frequency and Clinical Phenotype of BAP1 Hereditary Predisposition Syndrome

> **NCT04792463** · — · RECRUITING · sponsor: **Mohamed Abdel-Rahman** · enrollment: 500 (estimated)

## Conditions studied

- Uveal Melanoma
- Cutaneous Melanoma
- BAP1 Gene Mutation
- Renal Cell Carcinoma
- Mesothelioma
- Hepatocellular Carcinoma
- Cholangiocarcinoma
- Meningioma Atypical

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT04792463
- **Lead sponsor:** Mohamed Abdel-Rahman
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** RECRUITING
- **Start date:** 2015-03-03
- **Primary completion:** 2026-07-01
- **Final completion:** 2026-07-01
- **Target enrollment:** 500 (ESTIMATED)
- **Last updated:** 2026-03-09


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT04792463

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT04792463, "Frequency and Clinical Phenotype of BAP1 Hereditary Predisposition Syndrome". Retrieved via AI Analytics 2026-07-25 from https://api.ai-analytics.org/clinical/NCT04792463. Licensed CC0.

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