LivingGLP1
Study S002037

A Phase 3, Randomized, Double-Blind Extension Trial to Evaluate the Long-term Efficacy, Safety, and Tolerability of Maridebart Cafraglutide in Participants With Obesity or Overweight

Registration

Registration
NCT07684235
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
DOUBLE
Status
RECRUITING
Enrollment
3200
Start
2026-07-23
Primary completion
2027-12-26
Lead sponsor
Amgen
Conditions
Obesity; Overweight
Interventions
DRUG:Maridebart cafraglutide; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
YES

Registered primary outcomes

  • Percent Change in Body Weight from Baseline of the Parent Trial (20210181) [Baseline of parent trial (20210181) to Week 48 of current trial]
  • Number of Participants Experiencing Treatment-emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs) [Baseline of current trial up to 60 weeks]

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