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Completed Phase 2 Interventional Results available

Dose Ranging Efficacy And Safety With Mepolizumab in Severe Asthma

ClinicalTrials.gov ID: NCT01000506

Public ClinicalTrials.gov record NCT01000506. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 2, 2026, 6:34 AM EST

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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 identification

NCT ID
NCT01000506
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
621 participants

Conditions and interventions

Conditions

Interventions

Biological · Drug

Eligibility (public fields only)

Age range
12 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 1, 2009 (Type not available)
Primary completion
Mar 23, 2012 (Actual)
Completion
Mar 23, 2012 (Actual)
Last update posted
Jan 24, 2018

2009 – 2012

United States locations

U.S. sites
21
U.S. states
14
U.S. cities
21
Facility City State ZIP Site status
GSK Investigational Site Long Beach California 90808 —
GSK Investigational Site Los Angeles California 90095 —
GSK Investigational Site Riverside California 92506 —
GSK Investigational Site San Diego California 92103-8415 —
GSK Investigational Site Denver Colorado 80206 —
GSK Investigational Site New Haven Connecticut 06510 —
GSK Investigational Site Albany Georgia 31707 —
GSK Investigational Site Columbus Georgia 31904 —
GSK Investigational Site Lexington Kentucky 40508 —
GSK Investigational Site St Louis Missouri 63110 —
GSK Investigational Site Winston-Salem North Carolina 27103 —
GSK Investigational Site Canton Ohio 44718 —
GSK Investigational Site Cleveland Ohio 44195 —
GSK Investigational Site Oklahoma City Oklahoma 73103 —
GSK Investigational Site Hershey Pennsylvania 17033 —
GSK Investigational Site Pittsburgh Pennsylvania PA 15213 —
GSK Investigational Site Charleston South Carolina 29406 —
GSK Investigational Site Nashville Tennessee 37203 —
GSK Investigational Site Boerne Texas 78006 —
GSK Investigational Site Houston Texas 77054 —
GSK Investigational Site Madison Wisconsin 53792 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 73 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01000506, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 24, 2018 · Synced Nov 2, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01000506 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →