drugset / Trial / NCT06079671

Study of Volrustomig in Women With High Risk Locally Advanced Cervical Cancer (eVOLVE-Cervical)

NCT06079671

RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a phase III, randomized, double-blind, placebo-controlled, multi-center, global study to explore the efficacy and safety of volrustomig in women with high-risk LACC (FIGO 2018 stage IIIA to IVA cervical cancer) who have not progressed following platinum-based CCRT.

Timeline

Start
2023-09-22
Primary completion
2027-11-26
Completion
2030-09-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Volrustomig Monoclonal antibody Intravenous

Indications