drugset / Trial / NCT02135640

China HVT Safety, PK, PD

NCT02135640

Phase 1 Completed 64 enrolled GlaxoSmithKline
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

EvaluationDrugModalityDoseRoute
Subject Denosumab Monoclonal antibody 60 mg Subcutaneous
Subject Denosumab Monoclonal antibody 120 mg Subcutaneous

Indications