drugset / Trial / NCT04590599
A Phase II Clinical Study to Assess the Efficacy and Safety of IBI310 or Placebo Combined With Sintilimab for Advanced Cervical Cancer Subjects Who Have Failed or Cannot Tolerate First-line or Above Platinum-based Chemotherapy
RandomizedParallel-groupQuadruple-blindTreatment
Summary
This is a randomized, double-blind, controlled, parallel-cohort Phase II clinical study, which is planned to enroll 220 subjects with advanced cervical cancer who have failed or cannot tolerate first-line or above platinum-based chemotherapy
Timeline
- Start
- 2020-12-08
- Primary completion
- 2023-11-20
- Completion
- 2023-11-20
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | IBI310 | Monoclonal antibody | 3 mg/kg | Intravenous |
| Background | Sintilimab | Monoclonal antibody | 200 mg | Intravenous |