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ACTIVE NOT RECRUITING Phase 3

Evaluation of Maridebart Cafraglutide in Adult Participants Without Type 2 Diabetes Mellitus Who Have Obesity or Are Overweight

NCT06858839 · View on ClinicalTrials.gov ↗

Study Summary

The primary objective of this study is to demonstrate that maridebart cafraglutide is superior to placebo for percent change in body weight.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG Maridebart Cafraglutide

Study Locations (20)

California

  • Ark Clinical Research- Tustin — Fountain Valley
  • Long Beach Clinical Trials Services Inc — Long Beach
  • Ark Clinical Research- Long Beach — Long Beach
  • Catalina Research Institute — Montclair
  • Artemis Institute for Clinical Research — Riverside
  • Artemis Institute for Clinical Research — San Diego
  • Apex Clinical Research — San Diego
  • Southern California Clinical Research — Santa Ana
  • Diablo Clinical Research — Walnut Creek

Florida

  • Indago Research and Health Center — Hialeah
  • Jacksonville Center for Clinical Research — Jacksonville
  • Clinical Neuroscience Solutions - Jacksonville — Jacksonville
  • South Florida Wellness and Clinical Research Institute — Margate
  • Optimus U Corporation — Miami

Alabama

  • Pinnacle Research Group LLC — Anniston
  • Alliance For Multispecialty Research - Daphne — Daphne
  • Alliance for Multispecialty Research Mobile — Mobile

Connecticut

  • Yale School of Medicine — New Haven
  • Chase Medical Research LLC — Waterbury

Arizona

  • Avacare Foothills Research Center — Phoenix

Trial Details

FieldValue
Enrollment Target 3,853 participants
Start Date 2025-03-12
Est. Completion 2027-04-16
Phase Phase 3

Sponsor

Amgen

266 total trials

Interested in This Trial?

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06858839

The ClinicalTrials.gov registry entry for NCT06858839 describes a study currently listed as active not recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 3,853 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Amgen, which has 266 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Obesity appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06858839 reports 20 study locations spanning 5 distinct geographic areas — top geographies include California, Florida, Alabama. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06858839 about?

NCT06858839 is a clinical study titled "Evaluation of Maridebart Cafraglutide in Adult Participants Without Type 2 Diabetes Mellitus Who Have Obesity or Are Overweight". The primary objective of this study is to demonstrate that maridebart cafraglutide is superior to placebo for percent change in body weight.

What is the current status of trial NCT06858839?

This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 3,853 participants. The study started on 2025-03-12. Estimated completion is 2027-04-16.

What conditions does trial NCT06858839 study?

This clinical trial studies the following conditions: Obesity. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06858839?

The interventions under investigation include: Placebo (DRUG), Maridebart Cafraglutide (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06858839?

This trial is sponsored by Amgen, which has 266 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06858839 being conducted?

This trial has 20 study locations across Alabama, Arizona, California, Connecticut, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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