drugset / Trial / NCT04328831
Safety and Efficacy of IBI322 in Chinese Subjects With Advanced Malignant Tumors
NaSingle-groupOpen-labelTreatment
Summary
This is a phase I study evaluating the safety, tolerability and preliminary efficacy of IBI322 in cancer subjects who failed standard treatment.
Timeline
- Start
- 2020-07-31
- Primary completion
- 2023-08-28
- Completion
- 2023-08-28
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | IBI322 | Monoclonal antibody | — | — |