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A Study of LY3537021 in Healthy Participants and Participants With Type 2 Diabetes Mellitus

Primary Purpose

Healthy, Type 2 Diabetes Mellitus

Status
Completed
Phase
Phase 1
Locations
Singapore
Study Type
Interventional
Intervention
LY3537021
Placebo
Sponsored by
Eli Lilly and Company
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Healthy

Eligibility Criteria

21 Years - 70 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Are overtly healthy males or females not of childbearing potential, as determined through medical history and physical examination
  • Contraceptive use by men should also be consistent with local regulations regarding the methods of contraception for those participating in clinical studies.
  • Have a body mass index of 18.5 to 40 kilograms per square meter (kg/m²), inclusive
  • Have hemoglobin A1c level of less than or equal to (≤)6.5 percent (%)

Patients with Type 2 Diabetes Mellitus (T2DM):

  • Have T2DM for at least 6 months
  • For Part A, have a hemoglobin A1c value at screening of 6.5% to 11% and are treated with diet and exercise alone or a stable dose of metformin for at least 3 months prior to screening. For Part B, have hemoglobin A1c value at screening of 6.5% to 10% and are treated with diet and exercise alone or a stable dose of metformin for at least 3 months prior to screening with or without 1 other OAM, such as DPP-IV inhibitors, SGLT-2 inhibitors, or sulfonylureas

Exclusion Criteria:

  • Have an abnormality in the 12-lead electrocardiogram (ECG) that, in the opinion of the investigator, increases the risks associated with participating in the study or may confound ECG data analysis
  • Have a history of malignancy within 5 years prior to screening
  • Have obvious clinical signs or symptoms of liver disease, acute or chronic hepatitis
  • Have evidence of significant active psychiatric disorder(s) as determined by the investigator
  • Have undergone any form of bariatric surgery
  • Have donated blood of 450 milliliters (mL) or more in the past 3 months or any blood donation within the past month from screening
  • Have an average weekly alcohol intake that exceeds 21 units per week (males up to age 65 years) and 14 units per week (females and males above 65 years), or are unwilling to stop alcohol consumption 24 hours prior to dosing until discharge from the investigative site
  • Smoke >10 cigarettes per day or the equivalent or are unable or unwilling to refrain from nicotine during investigative site admission

Patients with T2DM:

  • Have had any of the following within the past 6 months prior to screening: myocardial infarction, unstable angina, coronary artery bypass graft, percutaneous coronary intervention (diagnostic angiograms are permitted), transient ischemic attack, cerebrovascular accident or decompensated congestive heart failure, or currently have New York Health Association Class III or IV heart failure
  • Are currently treated with or within the past 3 months had treatment with GLP-1 receptor agonists, or insulin
  • Have had severe hypoglycemic event in the last 3 months

Sites / Locations

  • Lilly Centre for Clinical Pharmacology

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm Type

Experimental

Experimental

Placebo Comparator

Experimental

Experimental

Placebo Comparator

Arm Label

LY3537021 (Part A/Healthy)

LY3537021 (Part A/Type 2 Diabetes)

Placebo (Part A)

LY3537021 (Part B/Healthy)

LY3537021 (Part B/Type 2 Diabetes)

Placebo (Part B)

Arm Description

LY3537021 administered subcutaneously (SC) to healthy participants.

LY3537021 administered SC to participants with type 2 diabetes mellitus (T2DM).

Placebo administered SC.

LY3537021 administered SC to healthy participants.

LY3537021 administered SC to participants with T2DM.

Placebo administered SC.

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 (AUC) of LY3537021
PK: AUC of LY3537021
PK: Maximum Concentration (Cmax) of LY3537021
PK: Cmax of LY3537021

Full Information

First Posted
October 12, 2020
Last Updated
December 16, 2021
Sponsor
Eli Lilly and Company
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1. Study Identification

Unique Protocol Identification Number
NCT04586907
Brief Title
A Study of LY3537021 in Healthy Participants and Participants With Type 2 Diabetes Mellitus
Official Title
A Single- and Multiple-Ascending Dose Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of LY3537021 in Healthy Participants and Patients With Type 2 Diabetes Mellitus
Study Type
Interventional

2. Study Status

Record Verification Date
December 2021
Overall Recruitment Status
Completed
Study Start Date
November 23, 2020 (Actual)
Primary Completion Date
November 30, 2021 (Actual)
Study Completion Date
November 30, 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
No
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 learn more about the safety of LY3537021 and any side effects that might be associated with it in healthy participants and participants with type 2 diabetes mellitus (T2DM). Blood tests will be performed to check how much LY3537021 gets into the bloodstream and how long the body takes to eliminate it. This study will last up to about 19 weeks including screening period.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Healthy, Type 2 Diabetes Mellitus

7. Study Design

Primary Purpose
Basic Science
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
85 (Actual)

8. Arms, Groups, and Interventions

Arm Title
LY3537021 (Part A/Healthy)
Arm Type
Experimental
Arm Description
LY3537021 administered subcutaneously (SC) to healthy participants.
Arm Title
LY3537021 (Part A/Type 2 Diabetes)
Arm Type
Experimental
Arm Description
LY3537021 administered SC to participants with type 2 diabetes mellitus (T2DM).
Arm Title
Placebo (Part A)
Arm Type
Placebo Comparator
Arm Description
Placebo administered SC.
Arm Title
LY3537021 (Part B/Healthy)
Arm Type
Experimental
Arm Description
LY3537021 administered SC to healthy participants.
Arm Title
LY3537021 (Part B/Type 2 Diabetes)
Arm Type
Experimental
Arm Description
LY3537021 administered SC to participants with T2DM.
Arm Title
Placebo (Part B)
Arm Type
Placebo Comparator
Arm Description
Placebo administered SC.
Intervention Type
Drug
Intervention Name(s)
LY3537021
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 119 (Part A) and Day 57 (Part B)
Secondary Outcome Measure Information:
Title
Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve (AUC) of LY3537021
Description
PK: AUC of LY3537021
Time Frame
Predose Day 1 through Day 119 (Part A) and Day 57 (Part B)
Title
PK: Maximum Concentration (Cmax) of LY3537021
Description
PK: Cmax of LY3537021
Time Frame
Predose Day 1 through Day 119 (Part A) and Day 57 (Part B)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Are overtly healthy males or females not of childbearing potential, as determined through medical history and physical examination Contraceptive use by men should also be consistent with local regulations regarding the methods of contraception for those participating in clinical studies. Have a body mass index of 18.5 to 40 kilograms per square meter (kg/m²), inclusive Have hemoglobin A1c level of less than or equal to (≤)6.5 percent (%) Patients with Type 2 Diabetes Mellitus (T2DM): Have T2DM for at least 6 months For Part A, have a hemoglobin A1c value at screening of 6.5% to 11% and are treated with diet and exercise alone or a stable dose of metformin for at least 3 months prior to screening. For Part B, have hemoglobin A1c value at screening of 6.5% to 10% and are treated with diet and exercise alone or a stable dose of metformin for at least 3 months prior to screening with or without 1 other OAM, such as DPP-IV inhibitors, SGLT-2 inhibitors, or sulfonylureas Exclusion Criteria: Have an abnormality in the 12-lead electrocardiogram (ECG) that, in the opinion of the investigator, increases the risks associated with participating in the study or may confound ECG data analysis Have a history of malignancy within 5 years prior to screening Have obvious clinical signs or symptoms of liver disease, acute or chronic hepatitis Have evidence of significant active psychiatric disorder(s) as determined by the investigator Have undergone any form of bariatric surgery Have donated blood of 450 milliliters (mL) or more in the past 3 months or any blood donation within the past month from screening Have an average weekly alcohol intake that exceeds 21 units per week (males up to age 65 years) and 14 units per week (females and males above 65 years), or are unwilling to stop alcohol consumption 24 hours prior to dosing until discharge from the investigative site Smoke >10 cigarettes per day or the equivalent or are unable or unwilling to refrain from nicotine during investigative site admission Patients with T2DM: Have had any of the following within the past 6 months prior to screening: myocardial infarction, unstable angina, coronary artery bypass graft, percutaneous coronary intervention (diagnostic angiograms are permitted), transient ischemic attack, cerebrovascular accident or decompensated congestive heart failure, or currently have New York Health Association Class III or IV heart failure Are currently treated with or within the past 3 months had treatment with GLP-1 receptor agonists, or insulin Have had severe hypoglycemic event in the last 3 months
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
Lilly Centre for Clinical Pharmacology
City
Singapore
ZIP/Postal Code
138623
Country
Singapore

12. IPD Sharing Statement

Plan to Share IPD
No
Links:
URL
https://trials.lillytrialguide.com/en-US/trial/7IMiImLoFJtACecUmt7d9Q
Description
A Study of LY3537021 in Healthy Participants and Participants With Type 2 Diabetes Mellitus

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