drugset / Trial / NCT06123884

BAT1308 Combined with Platinum-Based Chemotherapy± Bevacizumab for PDL1-Positive (CPS ≥1) Cervical Cancer

NCT06123884

Phase 2/3 Recruiting 526 enrolled Bio-Thera Solutions
RandomizedParallel-groupTriple-blindTreatment

Summary

Phase II study: a study to explore the safety and preliminary efficacy of BAT1308 combined with platinum-based chemotherapy ± Bevacizumab Phase III study: a confirmatory study to evaluate the safety and efficacy of BAT1308 combined with platinum-based chemotherapy ± Bevacizumab as first-line therapy for PD-L1-positive (CPS ≥ 1) persistent, recurrent or metastatic cervical cancer

Timeline

Start
2023-12-13
Primary completion
2026-09
Completion
2027-01

Drugs

EvaluationDrugModalityDoseRoute
Subject BAT1308 Monoclonal antibody 300 mg Intravenous
Subject Bevacizumab Injection Unknown 15 mg/kg
Background Carboplatin Small molecule
Background Cisplatin Other / unclassified
Background Paclitaxel for Injection Unknown

Indications