drugset / Trial / NCT02738489

A Study to Evaluate the Safety and Tolerability of Using the SHR-1210 in Patients With Advanced Melanoma

NCT02738489

Phase 1 Completed 36 enrolled Jiangsu HengRui Medicine Co., Ltd.
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This is an open-label, single center, non-randomized, dose escalation phase I trial to evaluate safety and tolerability of SHR-1210 (camrelizumab) in patients with advanced melanoma with disease progression after standard treatment, unresectable lesions, or metastases. Between Apr 13, 2016, and Jan 8, 2020, 36 patients were enrolled from Beijing Cancer Hospital.

Timeline

Start
2016-04-13
Primary completion
2020-01-08
Completion
2020-01-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Camrelizumab Monoclonal antibody 60 mg
Subject Camrelizumab Monoclonal antibody 200 mg
Subject Camrelizumab Monoclonal antibody 400 mg

Indications