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NCT07226778 · ClinicalTrials.gov registry record · Phase 1

Comparing the Extent to Which Maridebart Cafraglutide (AMG 133) is Made Available in the Body When Administered Using Two Subcutaneous (SC) Presentations

A Phase 1 study of Obesity and Overweight, sponsored by Amgen.

Active
Registry status
Phase 1
Development phase
348
Enrollment target
4
Study locations

NCT07226778 is a Phase 1 study of Obesity and Overweight that is active but no longer recruiting, run by Amgen. The registered enrollment target is 348 participants, below the 819-participant average among 1,053 other Obesity trials with a reported enrollment target (58% lower). The trial reports 4 study locations across 4 states.

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The verdict

NCT07226778, a Phase 1 study of Obesity and Overweight, is active but no longer recruiting, sponsored by Amgen.

ACTIVE NOT RECRUITING
Registry status
Phase 1
Development phase
348 participants
Enrollment target
4
Study locations

Study Summary

The main objective of this trial is to evaluate the pharmacokinetics (PK) of maridebart cafraglutide administered as a single dose using two different SC presentations in participants living with overweight or obesity.

Conditions Studied

Interventions

  • DRUG Maridebart Cafraglutide

Study Locations (4)

California

  • Anaheim Clinical Trials - Anaheim

Florida

  • Fortrea Clinical Research Unit - Daytona Beach - Daytona Beach

Texas

  • Fortrea Clinical Research Unit - Dallas - Dallas

Wisconsin

  • Fortrea Clinical Research Unit Inc. - Madison - Madison

Trial Details

FieldValue
Enrollment Target 348 participants
Start Date 2025-10-10
Est. Completion 2026-05-28
Phase Phase 1

Sponsor

Amgen

558 total trials

What the Registry Record Tells You About NCT07226778

The ClinicalTrials.gov registry entry for NCT07226778 describes a study currently listed as active not recruiting, categorized as Phase 1. The registered enrollment target is 348 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 819-participant average among 1,053 other Obesity trials with a reported enrollment target (58% lower). The listed sponsor is Amgen, which has 558 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Obesity appearing as the primary indexed condition, and to 1 intervention - of which Maridebart Cafraglutide is the first listed.

NCT07226778 reports 4 study locations spanning 4 distinct geographic areas - top geographies include California, Florida, Texas.

Frequently Asked Questions

What is clinical trial NCT07226778 about?

NCT07226778 is a clinical study titled "Comparing the Extent to Which Maridebart Cafraglutide (AMG 133) is Made Available in the Body When Administered Using Two Subcutaneous (SC) Presentations". The main objective of this trial is to evaluate the pharmacokinetics (PK) of maridebart cafraglutide administered as a single dose using two different SC presentations in participants living with overweight or obesity.

What is the current status of trial NCT07226778?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 348 participants. The study started on 2025-10-10. Estimated completion is 2026-05-28.

What conditions does trial NCT07226778 study?

This clinical trial studies the following conditions: Obesity, Overweight.

What interventions are being tested in trial NCT07226778?

The interventions under investigation include: Maridebart Cafraglutide (DRUG).

Who is sponsoring clinical trial NCT07226778?

This trial is sponsored by Amgen, which has 558 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07226778 being conducted?

This trial has 4 study locations across California, Florida, Texas, Wisconsin. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.