drugset / Trial / NCT07613567

A Clinical Study of QL1706 Combined With Chemotherapy as Neoadjuvant Therapy for High-Risk Locally Advanced Cervical Cancer

NCT07613567

Phase 3 Not yet recruiting 486 enrolled Fujian Cancer Hospital
RandomizedParallel-groupOpen-labelTreatment

Summary

This study aims to compare the efficacy and safety of "neoadjuvant immunotherapy combined with chemotherapy followed by immunotherapy combined with radiotherapy during the radiotherapy period" versus "standard concurrent chemoradiotherapy" in locally advanced cervical cancer.

Timeline

Start
2026-09-01
Primary completion
2032-08-31
Completion
2032-08-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Carboplatin Small molecule 1.5 unknown
Comparator Cisplatin Other / unclassified 25 mg/m2
Comparator Cisplatin Other / unclassified 40 mg/m2
Subject Iparomlimab Monoclonal antibody 5 mg/kg
Subject Paclitaxel Small molecule 90 mg/m2
Subject Tuvonralimab Monoclonal antibody 5 mg/kg

Indications