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Intravenous Mepolizumab In Subjects With Hypereosinophilic Syndromes (HES)

OverviewStructured DataIssuesContributors
Is a
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Clinical study
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Allocation Type
Randomized
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Health Conditions in Trial
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Hypereosinophilia
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Hypereosinophilic syndrome
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Intervention Model
Parallel Assignment
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Interventional Trial Phase
Phase 3
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Interventional Trial Purpose
Treatment
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Last Updated
May 5, 2020
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Masking Type
Double
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Primary Completion Date
May 1, 2006
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Trial Recruitment Size
86
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Trial Sponsor
GlaxoSmithKline
GlaxoSmithKline
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Clinical Trial Start Date
March 23, 2004
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Study Completion Date
May 1, 2006
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Clinical Trial Study Type
Interventional
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NCT Number
NCT00086658
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Official Name
A Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- Sparing Effects of Mepolizumab in Subjects With Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of Subjects With HES
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Official Website
clinicaltrials.gov/study...086658
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