LivingGLP1
Study S003311

A Phase 1/2 Randomized Placebo-Controlled Double-Blind Study to Investigate the Safety, Tolerability, Efficacy, Pharmacokinetics, and Pharmacodynamics of Subcutaneous Doses of MET097 in Adult Participants With Obesity and Overweight But Otherwise Healthy

Registration

Registration
NCT06857617
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1; PHASE2
Masking
DOUBLE
Status
COMPLETED
Enrollment
120
Start
2024-04-01
Primary completion
2025-01-03
Lead sponsor
Metsera, a wholly owned subsidiary of Pfizer
Conditions
Obesity and Overweight
Interventions
BIOLOGICAL:(Part C) MET097; BIOLOGICAL:(Part C) Placebo
Results posted
FALSE
Individual participant data sharing
UNDECIDED

Registered primary outcomes

  • (Part C) Percent change from baseline in body weight at Week 12 (Day 85). [Day 1 (Week 0) to Day 85 (Week 12)]

Linked records (0)

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