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NCT07160257 · ClinicalTrials.gov registry record · Phase 1

A Study to Evaluate the Effect of Maridebart Cafraglutide on Insulin Sensitivity and β-cell Function in Participants With Type 2 Diabetes Mellitus

A Phase 1 study of Type 2 Diabetes Mellitus, sponsored by Amgen.

Recruiting
Registry status
Phase 1
Development phase
70
Enrollment target
1
Study location

NCT07160257 is a Phase 1 study of Type 2 Diabetes Mellitus that is actively recruiting participants, run by Amgen. The registered enrollment target is 70 participants, below the 2,748-participant average among 122 other Type 2 Diabetes Mellitus trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT07160257, a Phase 1 study of Type 2 Diabetes Mellitus, is actively recruiting participants, sponsored by Amgen.

RECRUITING
Registry status
Phase 1
Development phase
70 participants
Enrollment target
1
Study location

Study Summary

The primary objective of this study is to determine the effect of maridebart cafraglutide relative to placebo on insulin sensitivity in participants with Type 2 Diabetes Mellitus (T2DM) treated with stable dose of metformin.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG Maridebart cafraglutide

Study Locations (1)

California

  • ProSciento, Inc. - Main Clinic - Chula Vista

Trial Details

FieldValue
Enrollment Target 70 participants
Start Date 2025-08-05
Est. Completion 2026-12-13
Phase Phase 1

Sponsor

Amgen

558 total trials

What the Registry Record Tells You About NCT07160257

The ClinicalTrials.gov registry entry for NCT07160257 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 70 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 2,748-participant average among 122 other Type 2 Diabetes Mellitus trials with a reported enrollment target (97% lower). The listed sponsor is Amgen, which has 558 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Type 2 Diabetes Mellitus appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT07160257 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT07160257 about?

NCT07160257 is a clinical study titled "A Study to Evaluate the Effect of Maridebart Cafraglutide on Insulin Sensitivity and β-cell Function in Participants With Type 2 Diabetes Mellitus". The primary objective of this study is to determine the effect of maridebart cafraglutide relative to placebo on insulin sensitivity in participants with Type 2 Diabetes Mellitus (T2DM) treated with stable dose of metformin.

What is the current status of trial NCT07160257?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 70 participants. The study started on 2025-08-05. Estimated completion is 2026-12-13.

What conditions does trial NCT07160257 study?

This clinical trial studies the following conditions: Type 2 Diabetes Mellitus.

What interventions are being tested in trial NCT07160257?

The interventions under investigation include: Placebo (DRUG), Maridebart cafraglutide (DRUG).

Who is sponsoring clinical trial NCT07160257?

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

Where is trial NCT07160257 being conducted?

This trial has 1 study location across California. 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.