deltatrials
Recruiting INTERVENTIONAL NCT07353931

Efficacy and Safety of Eloralintide (LY3841136) in Participants With Osteoarthritis Knee Pain and Obesity or Overweight (ENLIGHTEN-4)

A Master Protocol for Phase 3 Randomized, Double-Blind, Placebo-Controlled Studies to Investigate the Efficacy and Safety of Once Weekly Eloralintide in Adult Participants With Osteoarthritis Knee Pain, and Obesity or Overweight (ENLIGHTEN-4)

Sponsor: Eli Lilly and Company

Updated 2 times since 2026 Last updated: Apr 16, 2026 Started: Feb 9, 2026 Primary completion: Mar 1, 2028 Completion: May 1, 2028
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

A observational or N/A phase clinical study on Osteoarthritis and Overweight or Obesity, this trial is actively recruiting participants. The trial is conducted by Eli Lilly and Company and has accumulated 2 data snapshots since 2026. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.

Status Flow

~Feb 2026 – ~Apr 2026 · 2 months · monthly snapshotRecruitingApr 18, 2026 – present · 4 months · daily APIRecruiting

Change History

2 versions recorded
  1. Apr 18, 2026 — Present [daily]

    Recruiting

    Phase: PHASE3None

  2. Feb 2026 — Apr 2026 [monthly]

    Recruiting PHASE3

    First recorded

Eligibility Summary

The YDAN master protocol will support two independent studies, J3R-MC-YOA1 and J3R-MC-YOA2. Each study will investigate how well and safely Eloralintide (LY3841136) works in adults with obesity or overweight who have osteoarthritis (OA) of the knee with pain. Participation in the study will last about 75 weeks, including screening.

Contact Information

Sponsor contact:
  • Eli Lilly and Company
Data source: ClinicalTrials.gov

For direct contact, visit the study record on ClinicalTrials.gov .