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Completed Phase 2 Interventional Results available

Intravenous Mepolizumab In Children With Eosinophilic Esophagitis

ClinicalTrials.gov ID: NCT00358449

Public ClinicalTrials.gov record NCT00358449. 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, 1:45 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

A Randomized, Double-blind, Parallel Group Clinical Trial to Assess Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Intravenous Mepolizumab (SB240563)(0.55mg/kg, 2.5mg/kg or 10mg/kg) in Pediatric Subjects With Eosinophilic Esophagitis, Aged 2 to 17 Years (Study MEE103219)

Study identification

NCT ID
NCT00358449
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
84 participants

Conditions and interventions

Interventions

  • mepolizumab Drug

Drug

Eligibility (public fields only)

Age range
2 Years to 17 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 10, 2006
Primary completion
Nov 24, 2008
Completion
Nov 24, 2008
Last update posted
Jul 23, 2018

2006 – 2008

United States locations

U.S. sites
20
U.S. states
16
U.S. cities
19
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35205
GSK Investigational Site San Diego California 92123
GSK Investigational Site Tampa Florida 33613
GSK Investigational Site Atlanta Georgia 30322
GSK Investigational Site Springfield Illinois 62794
GSK Investigational Site Evansville Indiana 47713
GSK Investigational Site Indianapolis Indiana 46202
GSK Investigational Site Worcester Massachusetts 01655
GSK Investigational Site Southfield Michigan 48075
GSK Investigational Site Troy Michigan 48098
GSK Investigational Site Minneapolis Minnesota 55402
GSK Investigational Site Kansas City Missouri 64108
GSK Investigational Site St Louis Missouri 63104
GSK Investigational Site New York New York 10029
GSK Investigational Site Cincinnati Ohio 45229
GSK Investigational Site Sioux Falls South Dakota 57108
GSK Investigational Site Dallas Texas 75230
GSK Investigational Site Dallas Texas 75235
GSK Investigational Site Norfolk Virginia 23507
GSK Investigational Site Milwaukee Wisconsin 53215

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 9 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00358449, 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 23, 2018 · 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 NCT00358449 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →