LivingGLP1
Study S000839

A Phase 1, Single-ascending-dose Study to Evaluate the Safety and Pharmacokinetics of MEDI0382 in Healthy Volunteers

Registration

Registration
NCT02394314
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
362
Start
2015-02
Primary completion
2015-08
Lead sponsor
MedImmune LLC
Conditions
Healthy Volunteers
Interventions
DRUG:MEDI0382; DRUG:Placebo
Results posted
FALSE

Registered primary outcomes

  • Number of subjects with adverse events as a measure of safety and tolerability of MEDI0382 [28 days post dosing]
  • Number of subjects with Adverse events as a measure of safety and tolerability of MEDI0382 [28 days post dosing]

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