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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 |
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This study is available in CDISC format. |
September 2019 |