drugset / Trial / NCT06692166

A Study to Evaluate 9MW2821 Versus Treatment of Physician's Choice for Subjects With Recurrent or Metastatic Cervical Cancer

NCT06692166

Phase 3 Recruiting 420 enrolled Mabwell (Shanghai) Bioscience Co., Ltd.
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to compare the efficacy and safety of 9MW2821 and chemotherapy in participants with recurrent or metastatic cervical cancer who progressed on or after platinum-based chemotherapy.

Timeline

Start
2024-09-10
Primary completion
2027-12-09
Completion
2029-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Bulumtatug Fuvedotin Monoclonal antibody 1.25 mg/kg Intravenous
Comparator Gemcitabine Small molecule 1000 mg/m2 Intravenous
Comparator Pemetrexed Small molecule 500 mg/m2 Intravenous
Comparator Topotecan Small molecule 1 mg/m2 Intravenous
Comparator Topotecan Small molecule 1.25 mg/m2 Intravenous

Indications