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GSK-204958




An open label, randomised, three arm, single dose, multicentre, parallel group study in healthy subjects to compare the pharmacokinetics of subcutaneous mepolizumab when delivered as a liquid drug product in a safety syringe or an auto injector with a reconstituted lyophilised drug product from a vial
mepolizumab
204958
NCT03014674 2016-002405-19
Asthma
Phase 3
This study is available in CDISC format.
September 2019