drugset / Trial / NCT02492789
A Trial to Evaluate Safety and Tolerability of INCSHR01210 in Cancer Patients
NaSingle-groupOpen-labelTreatment
Summary
This is an open-label, multicenter, non-randomized, dose escalation and tumor-expansion phase I trial to evaluate safety and tolerability of INCSHR01210 in patients with advanced solid tumors. The trial will enroll subjects with advanced solid tumor who have failed current standard anti-tumor therapies.
Timeline
- Start
- 2015-09-01
- Primary completion
- 2019-03-01
- Completion
- 2019-07-05
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Camrelizumab | Monoclonal antibody | 1 mg/kg | Intravenous |
| Subject | Camrelizumab | Monoclonal antibody | 3 mg/kg | Intravenous |
| Subject | Camrelizumab | Monoclonal antibody | 10 mg/kg | Intravenous |
| Subject | Camrelizumab | Monoclonal antibody | 200 mg | Intravenous |