drugset / Trial / NCT07230626

SYS6002 vs Chemotherapy in Recurrent or Metastatic Cervical Cancer

NCT07230626

Phase 3 Not yet recruiting 412 enrolled CSPC Megalith Biopharmaceutical Co.,Ltd.
RandomizedParallel-groupOpen-labelTreatment

Summary

This study is a randomized, open-label, controlled, multicenter phase Ⅲ clinical trial, which aims to evaluate the efficacy and safety of SYS6002 versus investigator's choice of chemotherapy in the treatment of participants with recurrent or metastatic cervical cancer who have failed platinum-containing chemotherapy and PD-1/L1 inhibitor therapy

Timeline

Start
2025-11-20
Primary completion
2028-01-01
Completion
2028-07-01

Drugs

EvaluationDrugModalityDoseRoute
Comparator Docetaxel Small molecule 75 mg/m2 Intravenous
Comparator Gemcitabine Small molecule 1000 mg/m2 Intravenous
Comparator Pemetrexed Small molecule 500 mg/m2 Intravenous
Subject SYS6002 Other / unclassified Intravenous
Comparator Topotecan Small molecule 1.2 mg/m2 Intravenous

Indications