CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 621 enrolled
Drug / intervention
Mepolizumab 750 +3 morebiological
Likely dose
Mepolizumab 750 750mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01000506
NCT01000506Phase 2Completed

A Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel Group, Dose Ranging Study to Determine the Effect of Mepolizumab on Exacerbation Rates in Subjects With Severe Uncontrolled Refractory Asthma

GlaxoSmithKline·interventional·Posted Oct 23, 2009·Updated Jan 24, 2018

In Brief

A Phase 2 clinical trial evaluating Mepolizumab 750, Mepolizumab 250, and 2 other interventions for Asthma. Completed, enrolled 621 participants across 94 sites in 13 countries.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAsthma
CountriesArgentina, Australia, Canada, Chile, France, Germany, Poland, Romania, Russia, South Korea, Ukraine, United Kingdom, United States
Collaborators--

Timeline

Phase 2CompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedOct 23, 2009
Enrollment StartNov 1, 2009
Primary CompletionMar 23, 2012
TodayJul 2, 2026
Enrollment to primary: 2.4 yearsPosted 16.7 years ago

Interventions

Mepolizumab 750biological

Mepolizumab 750mg every four weeks by i.v.

Mepolizumab 250biological

Mepolizumab 250mg every four weeks by i.v.

Mepolizumab 75biological

Mepolizumab 75mg every four weeks by i.v.

Placebo salinedrug

Placebo saline every four weeks by i.v.