drugset / Trial / NCT01606163

Safety and Pharmacokinetics Study of Healthy Male Adults When Repeatedly Administered Through Intravenous Injection

NCT01606163

Phase 1 Completed 36 enrolled Green Cross Corporation
RandomizedParallel-groupDouble-blindPrevention

Summary

The purpose of this study is to evaluate the safety and pharmacokinetics of healthy male adults when subjects are repeatedly administered GC1102 (Hepabig\_Gene) through intravenous injection.

Timeline

Start
2012-08
Primary completion
2013-06
Completion
2013-12

Drugs

EvaluationDrugModalityDoseRoute
Subject LENVERVIMAB Monoclonal antibody 3 ml Intravenous
Subject LENVERVIMAB Monoclonal antibody 5 ml Intravenous
Subject LENVERVIMAB Monoclonal antibody 8 ml Intravenous
Subject LENVERVIMAB Monoclonal antibody 30000 iu Intravenous
Subject LENVERVIMAB Monoclonal antibody 50000 iu Intravenous
Subject LENVERVIMAB Monoclonal antibody 80000 iu Intravenous