drugset / Trial / NCT05044871

Summary

This study is an open-label, multicenter, umbrella study aimed to evaluate the combined, biomarker-driven, targeted treatment efficiency of Pamiparib, Bevacizumab, Tislelizumab, and Nab-paclitaxel in patients with platinum-resistant recurrent ovarian cancer (PROC).

Timeline

Start
2022-07-22
Primary completion
2025-02-17
Completion
2025-02-17

Drugs

EvaluationDrugModalityDoseRoute
Subject Bevacizumab Monoclonal antibody 7.5 mg/kg Intravenous
Subject Paclitaxel Small molecule 100 mg/m2 Intravenous
Subject Paclitaxel Small molecule 125 mg/m2 Intravenous
Subject Pamiparib Small molecule 40 mg Oral
Subject Tislelizumab Monoclonal antibody 200 mg Intravenous

Indications