Study S000839
A Phase 1, Single-ascending-dose Study to Evaluate the Safety and Pharmacokinetics of MEDI0382 in Healthy Volunteers
Registration
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]
Linked records (0)
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