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Active Not RecruitingNCT07229157

Effect of Maridebart Cafraglutide on the Heart's Electrical Activity

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

Status
Active Not Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
81 (actual)
Sponsor
Amgen · Industry
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

The main objective of this trial is to evaluate the effect of maridebart cafraglutide subcutaneously (SC) on the placebo-corrected, change from baseline in QT interval corrected for heart rate using Fridericia's formula in participants living with overweight or obesity.

Conditions

Interventions

TypeNameDescription
DRUGMaridebart CafraglutideParticipants will receive maridebart cafraglutide SC.
DRUGMoxifloxacinParticipants will receive moxifloxacin orally.
DRUGPlacebo for Maridebart CafraglutideParticipants will receive placebo for maridebart cafraglutide SC.
DRUGPlacebo for MoxifloxacinParticipants will receive placebo for moxifloxacin orally.

Timeline

Start date
2025-10-22
Primary completion
2026-08-26
Completion
2026-08-26
First posted
2025-11-14
Last updated
2026-01-23

Locations

2 sites across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT07229157. Inclusion in this directory is not an endorsement.