drugset / Trial / NCT02738489
A Study to Evaluate the Safety and Tolerability of Using the SHR-1210 in Patients With Advanced Melanoma
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Camrelizumab | Monoclonal antibody | 60 mg | — |
| Subject | Camrelizumab | Monoclonal antibody | 200 mg | — |
| Subject | Camrelizumab | Monoclonal antibody | 400 mg | — |