COsegregation of VARiants in Panel of Genes

Recruiting now · Not applicable

Conditions studied: Gene Mutation-Related Cancer, Genetic Predisposition

In brief

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 surgery.

Key facts

Study ID
NCT01689584
Run by
Institut Curie
People needed
11000
Starts
2012-07-02
Expected to finish
2038-01-02
Last updated by the study team
2026-05-27

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.