Clin2
NCT07478237Possibly a fitNot yet recruiting

Family cancer risk outreach and testing study

Genetic PredispositionFamily Members

Part of Genetic & congenital clinical trials.

This study helps people who carry a known cancer-related gene variant share information with their close family members. We offer free genetic testing to eligible relatives who have not yet been tested.

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

Phase
N/A
Enrollment
400 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You are 18 or older
  • You carry a pathogenic or likely pathogenic variant in a gene included in the Color Health Cancer Panel
  • You have at least one first- or second-degree relative (parent, sibling, child, grandparent, aunt/uncle, niece/nephew) living in the United States who has not had germline genetic testing
  • If you are a relative, you are 18 or older and live in the United States
  • If you are a relative, you have not had genetic testing within the last 5 years that included the specific variant

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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