LivingGLP1
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

Registration
NCT03341013
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
24
Start
2017-11-30
Primary completion
2018-01-29
Lead sponsor
MedImmune LLC
Conditions
Type 2 Diabetes Mellitus
Interventions
DRUG:MEDI0382 Formulation 2; DRUG:MEDI0382 Formulation 3
Results posted
FALSE

Registered primary outcomes

  • Area under the drug concentration curve [48 hours]
  • Maximum observed plasma concentration of MEDI0382 [48 hours]

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