A Study of Eloralintide (LY3841136) in Participants With Obesity or Overweight, and Type 2 Diabetes

Study acronym: ENLIGHTEN-2
StatusRecruiting
PhasePhase 3
Started

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Record History

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  1. Minor Trial sites reduced: 148 → 143 locations
  2. Minor Trial sites reduced: 157 → 148 locations
    • Eligibility criteria expanded, about 20 words
  3. Minor Study sites: 159 to 157v19
  4. Minor Site details revised at 5 of 159 sitesv18
  5. Minor Site details revised at 23 of 159 sitesv17
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  1. Minor Site details revised at 13 of 159 sitesv16
  2. Minor Site details revised at 11 of 159 sitesv15
  3. Minor Site details revised at 1 of 159 sitesv14
  4. Minor Site details revised at 1 of 159 sitesv13
  5. Minor Site details revised at 2 of 159 sitesv12
  6. Minor Study sites revised (159)v11
  7. Minor Study sites: 158 to 159v10
  8. Minor Site details revised at 2 of 158 sitesv9
  9. Minor Site details revised at 3 of 158 sitesv8
  10. Minor Study sites: 159 to 158v7
  11. Minor Site details revised at 24 of 159 sitesv6
  12. Minor Re-verified, no change to tracked fieldsv5
  13. Minor Site details revised at 2 of 159 sitesv4
  14. Minor Study Status, Referencesv3
  15. Notable Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 158 to 159
    • Start date changed from estimate of Jan 2026 to Dec 15, 2025
    v2
  1. Minor Study First Submitted
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
363 trials monitored
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The main purpose of this study is to evaluate the efficacy and safety of eloralintide compared with placebo for body weight reduction in participants with overweight or obesity and type 2 diabetes. Participation in the study will last about 75 weeks.
Trial Details
NCT Number NCT07282600
Lead Sponsor Eli Lilly and Company
Conditions
(from sponsor)
Overweight, Obesity
Related terms Diabetes Mellitus, Type 2, Obesity, Overweight
Enrollment 1,035 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov