drugset / Trial / NCT03691090

Study of SHR-1210 in Combination With Chemotherapy in Advanced Esophageal Cancer

NCT03691090 ↗

Phase 3 Completed 596 enrolled Jiangsu HengRui Medicine Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a randomised, double-blinded, placebo-controlled, multi-center phase III trial, comparing the efficacy and safety of SHR-1210 + paclitaxel + cisplatin vs placebo+paclitaxel +cisplatin as 1L therapy for advanced esophageal cancer patients in China. SHR-1210 is a humanized anti-PD1 IgG4 monoclonal antibody.

Timeline

Start
2018-12-03
Primary completion
2020-10-30
Completion
2022-04-30

Outcome

Met primary endpoint

paper overall survival for the camrelizumab-chemotherapy group was a median of 15.3 months (95% CI, 12.8-17.3; 135 deaths) vs a median of 12.0 months PMID 34519801 ↗

paper hazard ratio [HR] for death, 0.70 [95% CI, 0.56-0.88]; 1-sided P = .001 PMID 34519801 ↗

paper Progression-free survival for camrelizumab plus chemotherapy was a median of 6.9 months (95% CI, 5.8-7.4; 199 progression or deaths) vs 5.6 months PMID 34519801 ↗

paper HR for progression or death, 0.56 [95% CI, 0.46-0.68]; 1-sided P < .001 PMID 34519801 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Camrelizumab Monoclonal antibody 200 mg Intravenous
Background Cisplatin Other / unclassified 75 mg/m2 Intravenous
Background Paclitaxel Small molecule 175 mg/m2 Intravenous

Indications