drugset / Trial / NCT05798819

A Study of GLS-010 Plus Platinum-containing Chemotherapy±Bevacizumab as First-line Treatment for Persistent, Recurrent, or Metastatic Cervical Cancer

NCT05798819

Phase 3 Not yet recruiting 424 enrolled Guangzhou Gloria Biosciences Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a randomized, double-blind, placebo-controlled phase III study to evaluate GLS-010 plus platinum-containing chemotherapy with or without bevacizumab as first-line treatment for persistent, recurrent, or metastatic cervical cancer.

Timeline

Start
2023-05-01
Primary completion
2025-05-01
Completion
2026-12-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Zimberelimab Monoclonal antibody Intravenous
Comparator Bevacizumab Monoclonal antibody Intravenous
Background Carboplatin Small molecule Intravenous
Background Cisplatin Other / unclassified Intravenous
Background Paclitaxel Small molecule Intravenous

Indications

No indication recorded.