LivingGLP1
Study S000245

A Phase 1, Open-label, Randomized, Parallel Group Study to Assess the Relative Bioavailability of Two Maridebart Cafraglutide (AMG 133) Drug Products in Participants Living With Overweight or Obesity

Registration

Registration
NCT07832799
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
NOT_YET_RECRUITING
Enrollment
340
Start
2026-10-12
Primary completion
2027-03-23
Lead sponsor
Amgen
Conditions
Overweight; Obesity
Interventions
DRUG:Maridebart Cafraglutide
Results posted
FALSE
Individual participant data sharing
YES

Registered primary outcomes

  • Area Under the Concentration-Time Curve From Time 0 Extrapolated to Infinity (AUCinf) of Maridebart Cafraglutide [Up to Day 120]
  • Area Under the Concentration-Time Curve From Time 0 to the Time of the Last Quantifiable Concentration of Maridebart Cafraglutide [Up to Day 120]
  • Maximum Observed Concentration (Cmax) of Maridebart Cafraglutide [Up to Day 120]

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