A Phase 1 Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of LY4057996 in Healthy Participants and Participants With Type 1 and Type 2 Diabetes

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

⁃ Part A for Healthy Participants:

• Are overtly healthy as determined by medical evaluation, including medical history, physical exam, laboratory tests, and cardiac screening assessment

⁃ Part A for Type 2 Diabetes (T2DM) Participants:

• Are participants with T2DM diagnosed greater than 1 year before enrollment,

• On basal insulin therapy, insulin glargine, or insulin degludec, greater than 10 units per day for at least 6 months (for Cohort 5 only)

• Glycated hemoglobin (HbA1c) 6.5% to 9.5% inclusive at screening

⁃ Part B

• Have Type 1 Diabetes (T1D) for at least 1 year with a fasting C-peptide level of 0.20 nanomole per liter (nmol/L) or less or non-fasting C-peptide level of 0.30 nmol/L or less at screening

• HbA1c 6% to 8.5% inclusive at screening

⁃ Part C

• Have T1D for at least 1 year with a fasting C-peptide level of 0.20 nanomole per liter (nmol/L) or less or non-fasting C-peptide level of 0.30 nmol/L or less at screening

• HbA1c 6 to 8% inclusive at screening

⁃ All Parts

• Have blood pressure of less than 140/90 millimeters of mercury (mmHg) for healthy participants or 150/90 mmHg for participants with diabetes and pulse rate of less than 90 beats per minute (bpm) (supine)

• No hypoglycemia unawareness for all Type 1 and Type 2 Diabetes participants

Locations
Other Locations
Germany
Profil Institut für Stoffwechselforschung
RECRUITING
Neuss
Contact Information
Primary
Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or
LillyTrials@Lilly.com
1-317-615-4559
Backup
Physicians interested in becoming principal investigators please contact
clinical_inquiry_hub@lilly.com
Time Frame
Start Date: 2025-05-16
Estimated Completion Date: 2026-12
Participants
Target number of participants: 132
Treatments
Experimental: LY4057996 Part A (Cohorts A1-A5)
LY4057996 administered subcutaneously (SC) and/or intravenously (IV)
Placebo_comparator: Placebo Part A (Cohort A1-A5)
Placebo administered SC and/or IV
Experimental: LY4057996 Part B
LY4057996 administered SC
Experimental: LY4057996 Part C
LY4057996 and interventions of pre-study basal insulin and Lispro administered SC
Active_comparator: Degludec Part A (Cohort A2-A5)
Degludec administered SC and/or IV
Active_comparator: Degludec Part B
Degludec administered SC
Sponsors
Leads: Eli Lilly and Company

This content was sourced from clinicaltrials.gov

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