drugset / Trial / NCT05409326
A Study of TQH2722 Injection to Evaluate the Safety, Tolerability, Pharmacokinetics, Efficacy and Immunogenicity in Healthy Adult Subjects
Phase 1
Unknown
48 enrolled
Chia Tai Tianqing Pharmaceutical Group Nanjing Shunxin Pharmaceutical Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment
Summary
A randomized, double-blind, placebo-controlled trial design was used to assess the safety, tolerability, pharmacokinetics and pharmacodynamics characteristics, and immunogenicity of TQH2722 injection in healthy subjects.
Timeline
- Start
- 2022-06
- Primary completion
- 2023-06
- Completion
- 2023-08
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | TQH2722 | Monoclonal antibody | 50 mg | Subcutaneous |
| Subject | TQH2722 | Monoclonal antibody | 150 mg | Subcutaneous |
| Subject | TQH2722 | Monoclonal antibody | 300 mg | Subcutaneous |
| Subject | TQH2722 | Monoclonal antibody | 600 mg | Subcutaneous |
| Subject | TQH2722 | Monoclonal antibody | 1200 mg | Subcutaneous |