drugset / Trial / NCT05247619

A Clinical Study to Explore the Efficacy and Safety of Tislelizumab in Combination With Bevacizumab and Chemotherapy in Patients With Persistent, Recurrent, or Metastatic Cervical Cancer

NCT05247619 ↗

Phase 2 Unknown 49 enrolled Zhejiang Cancer Hospital
NaSingle-groupOpen-labelTreatment

Summary

Efficacy and safety of Tislelizumab combined with Bevacizumab and chemotherapy in patients with persistent, recurrent or metastatic cervical cancer.

Timeline

Start
2022-06-30
Primary completion
2024-08
Completion
2025-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Tislelizumab Monoclonal antibody 200 mg Intravenous
Background Bevacizumab Monoclonal antibody 7.5 mg/kg Intravenous
Background Carboplatin Small molecule 5 unknown Intravenous
Background Cisplatin Other / unclassified 50 mg/m2 Intravenous
Background Paclitaxel Small molecule 175 mg/m2 Intravenous

Indications