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A Study of Eloralintide (LY3841136) in Participants With Obesity, or Overweight Without Type 2 Diabetes
NCT07321886 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to evaluate the efficacy and safety of eloralintide in adults with obesity or overweight who do not have type 2 diabetes. The study has two phases: a main phase and an extension phase. Participation in the main phase of the study will last about 75 weeks. Participants with prediabetes will continue in the extension phase for another 2 years.
Conditions Studied
Interventions
- DRUG Placebo
- DRUG Eloralintide
Study Locations (20)
California
- Neighborhood Healthcare Institute of Health — Escondido
- Ark Clinical Research - Fountain Valley — Fountain Valley
- Desert Oasis Healthcare Medical Group — Palm Springs
- Peninsula Research Associates — Rolling Hills Estates
- Care Access - Sacramento — Sacramento
- Southern California Clinical Research — Santa Ana
- University Clinical Investigators, Inc. — Tustin
Florida
- JEM Research Institute — Atlantis
- BioMed Research & Medical Center — Miami
- Adult Medicine of Lake County, Inc. — Mt. Dora
- American Research Centers of Florida — Pembroke Pines
- AHF Pensacola — Pensacola
- IMA Clinical Research St. Petersburg — St. Petersburg
Georgia
- Teak Research Consults - Dunwoody — Dunwoody
- Teak Research Consults — Lawrenceville
- Clinical Research Atlanta — Stockbridge
Alabama
- MFA Clinical Research — Tuscaloosa
Arizona
- Headlands Research - Scottsdale — Scottsdale
Connecticut
- Chase Medical Research, LLC — Waterbury
Hawaii
- East-West Medical Research Institute — Honolulu
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,980 participants |
| Start Date | 2026-02-06 |
| Est. Completion | 2030-07 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07321886
The ClinicalTrials.gov registry entry for NCT07321886 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 1,980 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: NCT07321886 reports 20 study locations spanning 7 distinct geographic areas — top geographies include California, Florida, Georgia. 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 NCT07321886 about?
NCT07321886 is a clinical study titled "A Study of Eloralintide (LY3841136) in Participants With Obesity, or Overweight Without Type 2 Diabetes". The purpose of this study is to evaluate the efficacy and safety of eloralintide in adults with obesity or overweight who do not have type 2 diabetes. The study has two phases: a main phase and an extension phase. Participation in the main phase of the study will last about 75 weeks. Participants w...
What is the current status of trial NCT07321886?
This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 1,980 participants. The study started on 2026-02-06. Estimated completion is 2030-07.
What conditions does trial NCT07321886 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 NCT07321886?
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 NCT07321886?
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 NCT07321886 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.
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