drugset / Trial / NCT03710265
SHR-1701 in Metastatic or Locally Advanced Solid Tumors
NaSingle-groupOpen-labelTreatment
Summary
The main purpose of this Phase I study is to access the safety and tolerability of SHR-1701 at different dose levels. It is hoped to find out the recommended dose for Phase II/III.
Timeline
- Start
- 2018-11-20
- Primary completion
- 2022-12-31
- Completion
- 2022-12-31
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Retlirafusp alfa | Protein / enzyme biologic | 1 mg/kg | Intravenous |
| Subject | Retlirafusp alfa | Protein / enzyme biologic | 3 mg/kg | Intravenous |
| Subject | Retlirafusp alfa | Protein / enzyme biologic | 10 mg/kg | Intravenous |
| Subject | Retlirafusp alfa | Protein / enzyme biologic | 20 mg/kg | Intravenous |
| Subject | Retlirafusp alfa | Protein / enzyme biologic | 30 mg/kg | Intravenous |