drugset / Trial / NCT05855811

PREventing Second Cancers With DOSTARlimab

NCT05855811

Phase 2 Recruiting 400 enrolled Centre Leon Berard GlaxoSmithKline · collab
RandomizedParallel-groupOpen-labelPrevention

Summary

PredoSTAR is a multicenter, randomized, open-label phase II study proposed to patients at high risk of SPC and in whom the treatment of the FPC does not include immunotherapy. Dostarlimab treatment will be started within 6 months after the completion of treatment for localized FPC (i.e. after the end of last CT, RT cure or surgery with a wash-out period of 4 weeks before to start Dostarlimab). Eligible patients will be randomized (1:1) to receive: * Arm Dostarlimab : 4 intravenous (IV) injections of dostarlimab, Q3W or * Arm No treatment

Timeline

Start
2023-07-26
Primary completion
2028-07-26
Completion
2029-03-26

Drugs

EvaluationDrugModalityDoseRoute
Subject Dostarlimab Monoclonal antibody 500 mg Intravenous