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RECRUITING Phase 3

A Study of Eloralintide (LY3841136) in Participants With Persistent Obesity Who Are Treated With a Weekly Incretin

NCT07392190 · View on ClinicalTrials.gov ↗

Study Summary

The main purpose of this study is to evaluate the efficacy and safety of eloralintide compared with placebo in participants with persistent obesity or overweight, with or without type 2 diabetes, and on stable incretin background therapy. Participation in the study will last about 80 weeks.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG Eloralintide

Study Locations (20)

California

  • Irvine Clinical Research — Irvine
  • Scripps Whittier Diabetes Institute — La Jolla
  • Peninsula Research Associates — Rolling Hills Estates
  • Care Access - Sacramento — Sacramento
  • Artemis Institute for Clinical Research — San Diego
  • Southern California Clinical Research — Santa Ana
  • University Clinical Investigators, Inc. — Tustin

Florida

  • JEM Research Institute — Atlantis
  • AMR Clinical — Doral
  • Northeast Research Institute (NERI) — Fleming Island
  • Jacksonville Center for Clinical Research — Jacksonville
  • New Horizon Research Center — Miami
  • St Johns Center for Clinical Research — Saint Augustine

Arizona

  • RIO Clinical Trials - Phoenix — Phoenix
  • Headlands Research - Scottsdale — Scottsdale
  • Novak Clinical Research - Tucson - North La Cholla Boulevard — Tucson

Connecticut

  • New England Research Associates, LLC — Bridgeport
  • Yale University School of Medicine — New Haven
  • Chase Medical Research, LLC — Waterbury

Alabama

  • Birmingham Clinical Research — Birmingham

Trial Details

FieldValue
Enrollment Target 900 participants
Start Date 2026-02-10
Est. Completion 2028-07
Phase Phase 3

Sponsor

Eli Lilly and Company

704 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07392190

The ClinicalTrials.gov registry entry for NCT07392190 describes a study currently listed as 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 900 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Eli Lilly and Company, which has 704 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, 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: NCT07392190 reports 20 study locations spanning 5 distinct geographic areas — top geographies include California, Florida, Arizona. 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 NCT07392190 about?

NCT07392190 is a clinical study titled "A Study of Eloralintide (LY3841136) in Participants With Persistent Obesity Who Are Treated With a Weekly Incretin". The main purpose of this study is to evaluate the efficacy and safety of eloralintide compared with placebo in participants with persistent obesity or overweight, with or without type 2 diabetes, and on stable incretin background therapy. Participation in the study will last about 80 weeks.

What is the current status of trial NCT07392190?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 900 participants. The study started on 2026-02-10. Estimated completion is 2028-07.

What conditions does trial NCT07392190 study?

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

What interventions are being tested in trial NCT07392190?

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

Who is sponsoring clinical trial NCT07392190?

This trial is sponsored by Eli Lilly and Company, which has 704 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07392190 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