A Study of LY3457263 in Healthy Participants and Participants With Type 2 Diabetes
Primary Purpose
Healthy, Type 2 Diabetes
Status
Completed
Phase
Phase 1
Locations
Germany
Study Type
Interventional
Intervention
LY3457263
Dulaglutide
Placebo
Sponsored by

About this trial
This is an interventional basic science trial for Healthy
Eligibility Criteria
Inclusion Criteria:
- Males that agree to use an effective method of contraception or agree to remain abstinent
- Females that are not of childbearing potential due to postmenopausal status or due to surgical sterility
Part A only:
- Are overtly healthy
- Body mass index (BMI) of 18.5 to 35 kilograms per meter squared (kg/m²)
Part B only:
- Have been diagnosed with Type 2 Diabetes (T2D) for at least 6 months prior to screening
- Be treated for T2D with stable dose of metformin, a stable dose of a dipeptidyl peptidase-4 (DPP-4) inhibitor with or without metformin, or a stable dose of a glucagon-like peptide-1 (GLP-1) receptor agonist with or without metformin for at least 3 months prior to screening
- BMI of 27 to 40 kg/m²
Exclusion Criteria:
Have undergone any form of bariatric surgery
- Have used or intend to use medications that promote weight loss within 3 months prior to screening, for the duration of the study
Part A only:
- Have fasting plasma glucose (PG) levels ≥7 millimoles per liter (mmol/L) (≥126 milligrams per deciliter (mg/dL)) at screening
- Have Hemoglobin A1c (HbA1c) level ≥ 6.5% (48 millimoles per mole (mmol/mol)) at screening
- Have serum aspartate aminotransferase (AST) or alanine aminotransferase (ALT) >20% and 10%, above the upper limit of normal (ULN), respectively. Elevation of total bilirubin level is considered acceptable in case of Gilbert's disease (with a normal direct bilirubin)
Part B only:
- Have Type 1 Diabetes or latent autoimmune diabetes in adults
- Have uncontrolled diabetes defined as an episode of ketoacidosis or hyperosmolar state requiring hospitalization in the 6 months prior to screening
- Have known proliferative diabetic retinopathy, diabetic maculopathy, or severe nonproliferative diabetic retinopathy
- Present comorbid conditions commonly associated with diabetes (for example, hypertension, hypercholesterolemia, hypothyroidism) unless they are well-controlled with stable medication
- Have had an episode of severe hypoglycaemia within 6 months prior to screening, or have a history of hypoglycaemia unawareness or poor recognition of hypoglycaemia
- Have a history of acute or chronic pancreatitis or elevation in serum lipase and/or amylase >2 × ULN at screening
- Have a resting heart rate of <50 or >100 beats per minute
- Have an estimated glomerular filtration rate (<60 milliliter/minute (mL/min)/1.73 m2, or a level of estimated glomerular filtration rate that would contraindicate the use of metformin per the label in the respective country
- Have a screening calcitonin ≥20.0 picograms per milliliter (pg/mL)
- Fasting serum triglyceride level of >500 mg/dL at screening
- Have serum AST or ALT >3 × ULN or TBL >1.5 × ULN (except for participants diagnosed with Gilbert's syndrome)
- Have taken any prescription medication that are specifically indicated for lowering serum triglycerides within the last 3 months
- Have taken within the last 3 months any medications that interfere with absorption of dietary cholesterol or fats
- Use of medications known to prolong the QT/QTc interval
- Treated only with diet and exercise at study entry
Sites / Locations
- Profil Institut für Stoffwechselforschung
- Profil Mainz
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Experimental
Placebo Comparator
Experimental
Placebo Comparator
Arm Label
LY3457263 - Part A
Placebo - Part A
LY3457263 - Part B
Placebo - Part B
Arm Description
Escalating single doses of LY3457263 administered subcutaneously (SC) to healthy participants
Placebo administered SC to healthy participants
Escalating single doses of LY3457263 administered SC in combination with Dulaglutide administered SC to participants with type 2 diabetes
Placebo administered SC in combination with Dulaglutide administered SC to participants with type 2 diabetes
Outcomes
Primary Outcome Measures
Number of Participants with One or More Serious Adverse Event(s) (SAEs) Considered by the Investigator to be Related to Study Drug Administration
A summary of SAEs and other non-serious adverse events (AEs), regardless of causality, will be reported in the Reported Adverse Events module
Secondary Outcome Measures
Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve From Time Zero to Infinity (AUC[0-inf]) of LY3457263
PK: AUC[0-inf] of LY3457263
Full Information
NCT ID
NCT04641312
First Posted
November 20, 2020
Last Updated
January 10, 2022
Sponsor
Eli Lilly and Company
1. Study Identification
Unique Protocol Identification Number
NCT04641312
Brief Title
A Study of LY3457263 in Healthy Participants and Participants With Type 2 Diabetes
Official Title
A Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of LY3457263 in Healthy Participants and in Patients With Type 2 Diabetes
Study Type
Interventional
2. Study Status
Record Verification Date
January 1, 2022
Overall Recruitment Status
Completed
Study Start Date
November 25, 2020 (Actual)
Primary Completion Date
December 21, 2021 (Actual)
Study Completion Date
December 21, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Eli Lilly and Company
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The main purpose of this study is to investigate the safety and tolerability of the study drug LY3457263 in healthy participants and participants with type 2 diabetes. Blood tests will be performed to investigate how the body processes the study drug and how the study drug affects the body. The study has two parts (part A and B). Each part will last up to 10 weeks and may include up to either 13 (part A) or 19 (part B) visits.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Healthy, Type 2 Diabetes
7. Study Design
Primary Purpose
Basic Science
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
67 (Actual)
8. Arms, Groups, and Interventions
Arm Title
LY3457263 - Part A
Arm Type
Experimental
Arm Description
Escalating single doses of LY3457263 administered subcutaneously (SC) to healthy participants
Arm Title
Placebo - Part A
Arm Type
Placebo Comparator
Arm Description
Placebo administered SC to healthy participants
Arm Title
LY3457263 - Part B
Arm Type
Experimental
Arm Description
Escalating single doses of LY3457263 administered SC in combination with Dulaglutide administered SC to participants with type 2 diabetes
Arm Title
Placebo - Part B
Arm Type
Placebo Comparator
Arm Description
Placebo administered SC in combination with Dulaglutide administered SC to participants with type 2 diabetes
Intervention Type
Drug
Intervention Name(s)
LY3457263
Intervention Description
Administered SC
Intervention Type
Drug
Intervention Name(s)
Dulaglutide
Other Intervention Name(s)
LY2189265
Intervention Description
Administered SC
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Administered SC
Primary Outcome Measure Information:
Title
Number of Participants with One or More Serious Adverse Event(s) (SAEs) Considered by the Investigator to be Related to Study Drug Administration
Description
A summary of SAEs and other non-serious adverse events (AEs), regardless of causality, will be reported in the Reported Adverse Events module
Time Frame
Baseline through Day 42
Secondary Outcome Measure Information:
Title
Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve From Time Zero to Infinity (AUC[0-inf]) of LY3457263
Description
PK: AUC[0-inf] of LY3457263
Time Frame
Day 1 through Day 42
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Males that agree to use an effective method of contraception or agree to remain abstinent
Females that are not of childbearing potential due to postmenopausal status or due to surgical sterility
Part A only:
Are overtly healthy
Body mass index (BMI) of 18.5 to 35 kilograms per meter squared (kg/m²)
Part B only:
Have been diagnosed with Type 2 Diabetes (T2D) for at least 6 months prior to screening
Be treated for T2D with stable dose of metformin, a stable dose of a dipeptidyl peptidase-4 (DPP-4) inhibitor with or without metformin, or a stable dose of a glucagon-like peptide-1 (GLP-1) receptor agonist with or without metformin for at least 3 months prior to screening
BMI of 27 to 40 kg/m²
Exclusion Criteria:
Have undergone any form of bariatric surgery
Have used or intend to use medications that promote weight loss within 3 months prior to screening, for the duration of the study
Part A only:
Have fasting plasma glucose (PG) levels ≥7 millimoles per liter (mmol/L) (≥126 milligrams per deciliter (mg/dL)) at screening
Have Hemoglobin A1c (HbA1c) level ≥ 6.5% (48 millimoles per mole (mmol/mol)) at screening
Have serum aspartate aminotransferase (AST) or alanine aminotransferase (ALT) >20% and 10%, above the upper limit of normal (ULN), respectively. Elevation of total bilirubin level is considered acceptable in case of Gilbert's disease (with a normal direct bilirubin)
Part B only:
Have Type 1 Diabetes or latent autoimmune diabetes in adults
Have uncontrolled diabetes defined as an episode of ketoacidosis or hyperosmolar state requiring hospitalization in the 6 months prior to screening
Have known proliferative diabetic retinopathy, diabetic maculopathy, or severe nonproliferative diabetic retinopathy
Present comorbid conditions commonly associated with diabetes (for example, hypertension, hypercholesterolemia, hypothyroidism) unless they are well-controlled with stable medication
Have had an episode of severe hypoglycaemia within 6 months prior to screening, or have a history of hypoglycaemia unawareness or poor recognition of hypoglycaemia
Have a history of acute or chronic pancreatitis or elevation in serum lipase and/or amylase >2 × ULN at screening
Have a resting heart rate of <50 or >100 beats per minute
Have an estimated glomerular filtration rate (<60 milliliter/minute (mL/min)/1.73 m2, or a level of estimated glomerular filtration rate that would contraindicate the use of metformin per the label in the respective country
Have a screening calcitonin ≥20.0 picograms per milliliter (pg/mL)
Fasting serum triglyceride level of >500 mg/dL at screening
Have serum AST or ALT >3 × ULN or TBL >1.5 × ULN (except for participants diagnosed with Gilbert's syndrome)
Have taken any prescription medication that are specifically indicated for lowering serum triglycerides within the last 3 months
Have taken within the last 3 months any medications that interfere with absorption of dietary cholesterol or fats
Use of medications known to prolong the QT/QTc interval
Treated only with diet and exercise at study entry
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST)
Organizational Affiliation
Eli Lilly and Company
Official's Role
Study Director
Facility Information:
Facility Name
Profil Institut für Stoffwechselforschung
City
Neuss
State/Province
Nordrhein-Westfalen
ZIP/Postal Code
41460
Country
Germany
Facility Name
Profil Mainz
City
Mainz
ZIP/Postal Code
55116
Country
Germany
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
A Study of LY3457263 in Healthy Participants and Participants With Type 2 Diabetes
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