Status:
RECRUITING
COsegregation of VARiants in Panel of Genes
Lead Sponsor:
Institut Curie
Conditions:
Gene Mutation-Related Cancer
Genetic Predisposition
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The aim of the COVAR project is to classify reliably a maximum of VUS of the French database in order to use them for the genetic counseling. The results obtained through this study will have a major ...
Detailed Description
Originally, the COVAR study was designed to explore Variants of unknown biological significance (VUS) in BRCA1 (BReast Cancer 1) and BRCA2 (BReast Cancer 2) genes, which are the two major genes identi...
Eligibility Criteria
Inclusion
- Index cases:
- A person carrying a gene variant class 3 or 4, present and selected in the families of national database of genetic group and cancer (GGC Unicancer) which identifies the variations of all genes from the panel of genes of all French laboratories.
- Age ≥ 18 years.
- Signed written inform consent "index case"
- Related parties:
- Any relative of an index case with cancer
- Any relative without cancer related to an index case, retained by investigators, based on family structure and degree of related compared to the index case
- Age ≥ 18 years
- Information and signature of the informed consent "selected relatives"
Exclusion
- Minors
- Persons deprived of liberty or under guardianship (including curators).
- Absence of signed written inform consent
Key Trial Info
Start Date :
July 2 2012
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
January 2 2034
Estimated Enrollment :
3500 Patients enrolled
Trial Details
Trial ID
NCT01689584
Start Date
July 2 2012
End Date
January 2 2034
Last Update
April 6 2025
Active Locations (57)
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1
Institut Curie - Hopital Rene Huguenin
Saint-Cloud, Haut de Seine, France, 92210
2
CHU Amiens - Hôpital Nord
Amiens, France, 80054
3
ICO - Centre Paul Papin
Angers, France, 49933
4
Centre Hospitalier d'Angoulème
Angoulême, France, 16959