LivingGLP1
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

Registration
NCT05054530
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
73
Start
2021-11-11
Primary completion
2023-11-17
Lead sponsor
Gmax Biopharm Australia Pty Ltd.
Conditions
Overweight and Obesity
Interventions
DRUG:GMA106 Injection; DRUG:GMA106 Matching Placebo
Results posted
FALSE

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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