drugset / Trial / NCT01000506

Dose Ranging Efficacy And Safety With Mepolizumab in Severe Asthma

NCT01000506

Phase 2 Completed 621 enrolled GlaxoSmithKline
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to show whether mepolizumab given every 4 weeks intravenously (i.v.) can reduce the frequency of asthma exacerbations in subjects with severe asthma despite receiving high doses of standard asthma medications. The study will look at different doses of mepolizumab in comparison to a placebo.

Timeline

Start
2009-11-01
Primary completion
2012-03-23
Completion
2012-03-23

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Mepolizumab Monoclonal antibody 75 mg Intravenous
Comparator Mepolizumab Monoclonal antibody 250 mg Intravenous
Comparator Mepolizumab Monoclonal antibody 750 mg Intravenous

Indications