LivingGLP1
Study S001539

A Phase 1, Randomized, Double-blind, Placebo- and Positive-controlled, Parallel Group Study With Nested Crossover Comparison to Assess the Effect of Maridebart Cafraglutide on QT/QTc Intervals in Participants Living With Overweight or Obesity

Registration

Registration
NCT07229157
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
81
Start
2025-10-22
Primary completion
2026-08-27
Lead sponsor
Amgen
Conditions
Overweight; Obesity
Interventions
DRUG:Maridebart Cafraglutide; DRUG:Moxifloxacin; DRUG:Placebo for Maridebart Cafraglutide; DRUG:Placebo for Moxifloxacin
Results posted
FALSE
Individual participant data sharing
YES

Registered primary outcomes

  • Change from Baseline in QTcF for Maridebart Cafraglutide [Up to Day 171]

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