Study S003383
A PHASE 1, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO ASSESS THE SAFETY, TOLERABILITY AND PHARMACOKINETICS OF GMA106 IN HEALTHY, OVERWEIGHT AND OBESE ADULTS
Registration
Registered primary outcomes
- Nature, incidence and severity of treatment emergent adverse events [up to 150±5 days post injection]
- Nature, incidence and severity of treatment emergent adverse events [up to 227±5 days post first injection]
Linked records (0)
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