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A Trial to Evaluate Interactions Between Antiemetic Medication and AMG 133 in Participants Living With Overweight or Obesity

← catalyst calendar

NCT07310563

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

Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Randomized · None · Basic science
Enrollment
59actual
Sites
1
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
Start2024-12-10actualWhen the study began enrolling
Primary completion2025-05-09actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-05-09actualThe whole study's end, after follow-up
First posted2025-12-30actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-12-30actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Overweight
  • Obesity

Interventions

  • Drug: AMG 133
  • Drug: Ondansetron

Primary outcomes

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

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