drugset / Trial / NCT02135640
China HVT Safety, PK, PD
RandomizedParallel-groupSingle-blindTreatment
Summary
This study is to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of denosumab administered subcutaneously to healthy adults in China.
Timeline
- Start
- 2014-07-17
- Primary completion
- 2015-02-17
- Completion
- 2015-02-17
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Denosumab | Monoclonal antibody | 60 mg | Subcutaneous |
| Subject | Denosumab | Monoclonal antibody | 120 mg | Subcutaneous |