LivingGLP1
Study S001779

A Phase 2 Randomized, Placebo-controlled, Double-blind, Dose-ranging Study to Evaluate the Efficacy, Safety, and Tolerability of AMG 133 in Adult Subjects With Overweight or Obesity, With or Without Type 2 Diabetes Mellitus

Registration

Registration
NCT05669599
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
592
Start
2023-01-18
Primary completion
2024-10-08
Lead sponsor
Amgen
Conditions
Obesity; Overweight; Type 2 Diabetes Mellitus
Interventions
BIOLOGICAL:Maridebart Cafraglutide; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
CTIS:2023-510470-13-00; NIH:2023

Registered primary outcomes

  • Percent Change From Baseline to Week 52 in Body Weight [Baseline and Week 52]

Linked records (1)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.
RecordTitleYearDesignIdentifiersLink basis
R0010656Once-Monthly Maridebart Cafraglutide for the Treatment of Obesity - A Phase 2 Trial.
Jastreboff AM, The New England journal of medicine
2025Randomized trialPMID 40549887DOIcites ClinicalTrials.gov:NCT05669599; registry reference BACKGROUND:40549887