COsegregation of VARiants in Panel of Genes

Recruiting N/A Interventional Study
Gene Mutation-Related Cancer Genetic Predisposition
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Diagnostic
Participants needed
11,000 (estimated)
Sponsor
Institut Curie · Other
Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial
The aim of the COVAR project is to achieve reliable classification of as many variants of interest as possible from the French OncoGenetics Database (FrOG, https://frog-db.fr/) in order to use them for the genetic counseling. The results obtained through this study will have a major impact on clinical management of the patients and their families conducting in some cases to propose a prophylactic …
Trial Locations
Loading…

Loading trial locations…

Eligibility Criteria
Inclusion Criteria: Index cases: * A person carrying a variant of interest in a gene analyzed in a diagnostic setting by one of the laboratories within the Genetics and Cancer Group (GGC)-Unicancer network, classified as class 3, 4 or hypomorphic class 5, and selected by the national expert group …
Contacts

Sandrine CAPUTO, PhD

33172389367

sandrine.caputo@curie.fr

CONTACT

Isabelle TURBIEZ, Project Manager

33147111659

isabelle.turbiez@curie.fr

CONTACT