Clin2
NCT04431024Possibly a fitRecruiting

Testing imaging and biopsy options for people with BAP1 risk

Familial CancerBRCA1-Associated Protein-1 (BAP1) MutationsTumor Predisposition Syndrome (TPDS)Mesothelioma

Part of Cancer clinical trials.

This study looks at how well advanced scans, liquid biopsy tests, and small follow-up procedures can find early mesothelioma in people with a high-risk BAP1 gene condition. It may help catch cancer earlier when treatment could work better.

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

Phase
N/A
Enrollment
300 people
Ages
30 years to 120 years
Study type
Observational

Who can take part

  • Be age 30 or older
  • You have a known or suspected inherited BAP1 gene risk (BAP1 tumor predisposition) OR are a close family member (parent/sibling/child/grandparent/niece/nephew) of someone with a confirmed BAP1 condition
  • Understand the study and agree to sign a consent form
  • Have finished the study’s earlier genetic testing step showing a BAP1 (or other related inherited) mutation
  • Have already joined the related parent study (protocol 06C0014) for thoracic cancer risk testing

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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