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NCT06916065 · ClinicalTrials.gov registry record · Phase 1

A Study of Eloralintide (LY3841136) and Eloralintide With Tirzepatide in Participants With Overweight or Obesity

A Phase 1 study, sponsored by Eli Lilly and Company.

Completed
Registry status
Phase 1
Development phase
188
Enrollment target

NCT06916065: Completed Phase 1 study, sponsored by Eli Lilly and Company.

NCT06916065 is a Phase 1 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 188 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (213% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06916065, a Phase 1 study, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 1
Development phase
188 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate how well eloralintide and eloralintide with tirzepatide is tolerated and what side effects may occur in participants with overweight or obesity. The study drug will be administered subcutaneously (SC) (under the skin). Blood tests will be performed to check how much eloralintide and eloralintide with tirzepatide get into the bloodstream and how long it takes the body to eliminate it. There will be 6 cohorts. The study will last up to approximately 26 weeks, excluding screening for Cohorts A and B, 11 weeks for Cohorts C and D, and 12 weeks for Cohorts E and F.

Primary Outcome

PK: AUC of Eloralintide and Tirzepatide

Interventions

  • DRUG Eloralintide
  • DRUG Eloralintide and Tirzepatide

Trial Details

FieldValue
Enrollment Target 188 participants
Start Date 2025-04-09
Est. Completion 2026-01-19
Phase Phase 1
Eli Lilly and Company

1,341 total trials

What the finished NCT06916065 record still lists

NCT06916065 is an interventional study that assigns participants to a tested intervention. The registered 188 participants enrollment target is mid-sized for trials with a published cap, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (213% higher).

The record links to 0 conditions, and to 2 interventions - of which Eloralintide is the first listed.

NCT06916065 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06916065 about?

NCT06916065 is a clinical study titled "A Study of Eloralintide (LY3841136) and Eloralintide With Tirzepatide in Participants With Overweight or Obesity". The purpose of this study is to evaluate how well eloralintide and eloralintide with tirzepatide is tolerated and what side effects may occur in participants with overweight or obesity. The study drug will be administered subcutaneously (SC) (under the skin). Blood tests will be performed to check h...

What is the current status of trial NCT06916065?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 188 participants. The study started on 2025-04-09. Estimated completion is 2026-01-19.

What interventions are being tested in trial NCT06916065?

The interventions under investigation include: Eloralintide (DRUG), Eloralintide and Tirzepatide (DRUG).

Who is sponsoring clinical trial NCT06916065?

This trial is sponsored by Eli Lilly and Company, which has 1,341 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06916065's enrollment target sits among peer trials

188 289th of 2000 higher than 1,711 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06916065, the US trial registry maintained by the National Library of Medicine. NCT06916065 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.