drugset / Trial / NCT05584137

Evaluate the Efficacy, Safety and Tolerability of HLX26 and Serplulimab in Patients with MCRC

NCT05584137

Phase 2 Terminated 2 enrolled Shanghai Henlius Biotech
Non-randomizedSequentialOpen-labelTreatment

Summary

This study is a phase II study to evaluate the efficacy, safety and tolerability of HLX26 and HLX10 in the treatment of patients with metastatic colorectal carcinoma that had received 3 prior therapies.

Timeline

Start
2023-06-15
Primary completion
2023-12-31
Completion
2023-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject HLX26 Monoclonal antibody 500 mg Intravenous
Subject HLX26 Monoclonal antibody 800 mg Intravenous
Subject HLX26 Monoclonal antibody 1600 mg Intravenous
Subject Serplulimab Monoclonal antibody 300 mg Intravenous

Indications