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Terminated Phase 3 Interventional Results available

Open-Label Extension Of Intravenous Mepolizumab In Patients With Hypereosinophilic Syndrome

ClinicalTrials.gov ID: NCT00097370

Public ClinicalTrials.gov record NCT00097370. 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 Jul 21, 2026, 6:52 PM EDT

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

Official title

An Open Label Extension Study to Evaluate Safety and Efficacy of Mepolizumab in Patients With Hypereosinophilic Syndromes

Study identification

NCT ID
NCT00097370
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
78 participants

Conditions and interventions

Interventions

  • mepolizumab Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 75 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
Sep 29, 2004
Primary completion
Sep 28, 2010
Completion
Sep 28, 2010
Last update posted
Jul 6, 2017

2004 – 2010

United States locations

U.S. sites
10
U.S. states
10
U.S. cities
10
Facility City State ZIP Site status
GSK Investigational Site San Diego California 92103
GSK Investigational Site Denver Colorado 80206
GSK Investigational Site Bethesda Maryland 20892
GSK Investigational Site Boston Massachusetts 02215
GSK Investigational Site Rochester Minnesota 55905
GSK Investigational Site Cincinnati Ohio 45229
GSK Investigational Site Nashville Tennessee 37203-1424
GSK Investigational Site Salt Lake City Utah 84132
GSK Investigational Site Richmond Virginia 23298
GSK Investigational Site Madison Wisconsin 53705

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 14 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00097370, 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 Jul 6, 2017 · Synced Jul 21, 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 protocol, eligibility criteria, and contact information for NCT00097370 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →