drugset / Trial / NCT05173883
A Phase 1 Clinical Study of CU-20401 in Chinese Healthy Population
Non-randomizedSequentialOpen-labelTreatment
Summary
This is an open-label, Part I/2/3/4 Phase 1 clinical study to evaluate the safety, tolerability, pharmacokinetics, and immunogenicity of a single subcutaneous injection of CU-20401 in healthy Chinese population, and to recommend an appropriate dose for subsequent clinical studies.
Timeline
- Start
- 2021-12-20
- Primary completion
- 2023-11-02
- Completion
- 2023-11-02
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | CU-20401 | Unknown | 0.04 mg | Subcutaneous |
| Subject | CU-20401 | Unknown | 0.075 mg | Subcutaneous |
| Subject | CU-20401 | Unknown | 0.1 mg | Subcutaneous |
| Subject | CU-20401 | Unknown | 0.12 mg | Subcutaneous |
| Subject | CU-20401 | Unknown | 0.15 mg | Subcutaneous |
Indications
No indication recorded.