Study S001201
A Phase 1, Randomized, Cross-over, Two-period Pilot Study Investigating Bioequivalence Between a Single Dose of Formulation 2 and Formulation 3 of MEDI0382 in Healthy Adult Subjects
Registration
Registered primary outcomes
- Area under the drug concentration curve [48 hours]
- Maximum observed plasma concentration of MEDI0382 [48 hours]
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