A Study of LY4057996 in Healthy Participants and Participants With Type 1 and Type 2 Diabetes

Study acronym: YKAA
StatusRecruiting
PhasePhase 1
Started

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Trial flagged as At Risk
Primary completion moved at least 2 months later Dec 2026 → Mar 2027
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Record History

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  1. Minor Primary and study completion pushed from Dec 2026 to Mar 2027
    • Eligibility criteria expanded, about 15 words
  2. Minor Enrollment target: 132 to 124
    • Eligibility criteria expanded, about 6 words
    v9
  3. Minor 3 versions Re-verified since Sep 2, 2025, no change to tracked fieldsv6-v8
  4. Minor Site details revisedv5
  5. Minor Re-verified, no change to tracked fieldsv4
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  1. Notable Trial status: Not Yet Recruiting to Recruiting
    • Primary and study completion dates: Aug 2026 to Dec 2026
    • Start date changed from estimate of May 2025 to May 16, 2025
    • Site details revised
    v3
  2. Minor Site contact updatedv2
  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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2,236 trials monitored
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The purpose of this study is to evaluate how well LY4057996 is tolerated and what side effects may occur in healthy participants and participants with Type 1 and Type 2 Diabetes. The study drug will be administered either subcutaneously (SC) (under the skin) or intravenously (IV) (into a vein in the arm). Blood tests will be performed to check how much LY4057996 gets into the bloodstream and how long it takes the body to eliminate it. The study will last 11 weeks for Part A1-A2, 4 weeks for A3-A5, 6 weeks for Part B and 7 weeks for Part C, all approximations, excluding a screening period.
Trial Details
NCT Number NCT06945406
Lead Sponsor Eli Lilly and Company
Conditions
(from sponsor)
Diabetes Mellitus, Type 1, Diabetes Mellitus, Type 2
Related terms Diabetes Mellitus, Type 1, Diabetes Mellitus, Type 2
Enrollment 124 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov