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RecruitingNCT06152731

HRD Tests for Ovarian cancER

Status
Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
88 (estimated)
Sponsor
Centre Francois Baclesse · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The study concerns patients with Invasive epithelial ovarian cancer, primary Fallopian tube carcinoma, ovarian-type peritoneal carcinoma, and with an indication of a first-line platinum-based chemotherapy. To determine HRD status, 2 separate tests will be performed in the study: 1. Giscar assay : developed by the sponsor 2. myChoice assay If one or two tests identifies a HRD status : a PARP inhibitor treatment may be initiated according to current recommendations

Conditions

Interventions

TypeNameDescription
GENETICtests to determine HRD statusTest Giscar AND test myChoice will be performed. If one or two tests identifies a HRD status : a PARP inhibitor treatment may be initiated according to current recommendations

Timeline

Start date
2024-02-15
Primary completion
2031-06-01
Completion
2031-06-01
First posted
2023-12-01
Last updated
2025-09-17

Locations

4 sites across 1 country: France

Source: ClinicalTrials.gov record NCT06152731. Inclusion in this directory is not an endorsement.

HRD Tests for Ovarian cancER (NCT06152731) · Clinical Trials Directory