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A Trial to Assess the Effect of Kidney Impairment on How AMG 133 is Absorbed, Broken Down, and Eliminated by the Body

← catalyst calendar

NCT07429045

Sponsored by Amgen (industry) · AMGN — their whole pipeline →.

Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
44actual
Sites
5
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2025-03-11actualWhen the study began enrolling
Primary completion2025-11-21actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-11-21actualThe whole study's end, after follow-up
First posted2026-02-24actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-02-24actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Overweight and Obesity

Intervention

  • Drug: AMG 133 — also filed as Maridebart cafraglutide

Primary outcomes

what the primary-completion date above is the date OF
Maximum Observed Concentration (Cmax) of AMG 133
measured Up to Day 120
Area Under the Concentration-time Curve From Time 0 to the Time of the Last Quantifiable Concentration (AUClast) of AMG 133
measured Up to Day 120
AUC From Time 0 Extrapolated to Infinity (AUCinf) of AMG 133
measured Up to Day 120

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