ID
22722
Description
Study part: Adverse Events Run-In Visits. A Phase 2 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 Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.
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Versions (1)
- 6/11/17 6/11/17 -
Copyright Holder
GlaxoSmithKline
Uploaded on
June 11, 2017
DOI
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License
Creative Commons BY-NC 3.0
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Adverse Events Run-In Visits Mepolizumab HES NCT00086658
Adverse Events Run-In Visits
- StudyEvent: ODM
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