drugset / Trial / NCT01583530

Study of Belimumab Administered Subcutaneously to Healthy Subjects

NCT01583530

Phase 1 Completed 118 enrolled Human Genome Sciences Inc. GlaxoSmithKline · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to measure the amount of belimumab in the blood when given as an injection under the skin (subcutaneously; SC) and to evaluate the safety and tolerability of multiple injections under the skin in healthy subjects.

Timeline

Start
2011-02
Primary completion
2011-09
Completion
2011-09

Drugs

EvaluationDrugModalityDoseRoute
Comparator Belimumab Monoclonal antibody 200 mg Intravenous
Comparator Belimumab Monoclonal antibody 240 mg Intravenous

Indications

No indication recorded.