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Study identifier: NCT01689584 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

COsegregation of VARiants in Panel of Genes

Condition: Gene Mutation-Related Cancer · Genetic Predisposition  ·  Sponsor: Institut Curie

PhaseNA
Planned participants11000
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Sandrine CAPUTO, PhD  ·  33172389367  ·  sandrine.caputo@curie.fr

Isabelle TURBIEZ, Project Manager  ·  33147111659  ·  isabelle.turbiez@curie.fr

Always discuss trial participation with your own doctor first.

Locations (62)

Centre Hospitalier de BastiaBastia, Corsica, FranceNot Yet Recruiting
Institut Curie - Saint-Cloud siteSaint-Cloud, Haut de Seine, FranceRecruiting
CHU Amiens - Hôpital NordAmiens, FranceRecruiting
ICO - Centre Paul PapinAngers, FranceRecruiting
Centre Hospitalier d'AngoulèmeAngoulême, FranceRecruiting
Institut Sainte-CatherineAvignon, FranceRecruiting
CHU BesançonBesançon, FranceRecruiting
Groupe Hospitalier PellegrinBordeaux, FranceRecruiting
Institut BergoniéBordeaux, FranceRecruiting
Centre Hospitalier Jacques CoeurBourges, FranceRecruiting
CHU Morvan de BrestBrest, FranceRecruiting
Centre François BaclesseCaen, FranceRecruiting

+ 50 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT01689584