Clin2
NCT04792463Possibly a fitRecruiting

BAP1 gene cancer-risk study and family cancer patterns

Uveal MelanomaCutaneous MelanomaBAP1 Gene MutationRenal Cell CarcinomaMesotheliomaHepatocellular CarcinomaCholangiocarcinomaMeningioma Atypical

Part of Cancer, Digestive system, Eyes & vision, Kidney & urinary, Skin, Women’s health & pregnancy clinical trials.

This study looks at how the BAP1 gene affects cancer risk and what cancers people develop, including within families. You may be able to join if you have a known BAP1-related mutation, a strong family cancer history, or a concerning cancer pattern linked to BAP1.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
500 people
Ages
Any age
Study type
Observational

Who can take part

  • You have a known BAP1 pathogenic (harmful) or likely harmful gene variant, or a documented BAP1-related case in your family
  • OR you have had at least one cancer that can occur with BAP1 and at least two close relatives with BAP1-related cancers
  • OR you have had two or more BAP1-related cancers yourself
  • OR you are a close relative of someone with a documented BAP1 mutation (even if you never had cancer)
  • You can participate in an English consent process (the study materials are only available in English)

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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