A Study of LY3209590 in Healthy Participants and Participants With Type 2 Diabetes

NCT02942914 | Completed Phase 1

• 3 other identifiers: 16129I8H-MC-BDCA2016-001048-20
• Study Type: interventional
• Target: 80
• Locations: 1 country
• Sites: 1

Brief Summary

This trial is conducted to evaluate the safety of a study drug given by injection under the skin to healthy participants and participants with type 2 diabetes. It will also investigate how the body processes the study drug and the effect of the study drug on blood sugar levels. Information about any side effects and tolerability will be documented. This study is approximately 30 days for each participant, not including screening. Screening is required within 28 days prior to the start of the study.

Conditions

Diabetes Mellitus, Type 2

Outcome Measures

Primary Outcomes (1)

• Number of Participants with One or More Serious Adverse Event(s) (SAEs) Considered by the Investigator to be Related to Study Drug Administration

  Baseline through Day 31

Secondary Outcomes (2)

• Pharmacokinetics: Area Under The Concentration Curve Zero to Infinity (AUC[0-∞]) of LY3209590

  Baseline through Day 31

• Pharmacodynamics: Average Glucose from 8-Point Glucose Profiles in Participants with T2DM treated with Placebo or LY3209590

  Day 3

Study Arms (3)

LY3209590

EXPERIMENTAL

LY3209590 administered subcutaneously (SC).

Drug: LY3209590

Placebo

PLACEBO COMPARATOR

Placebo (sterile saline) administered SC.

Drug: Placebo

Insulin Glargine (Lantus)

ACTIVE COMPARATOR

Insulin Glargine administered SC.

Drug: Insulin Glargine

Interventions

LY3209590 DRUG

Administered SC

LY3209590

Placebo DRUG

Administered SC

Placebo

Insulin Glargine DRUG

Administered SC

Insulin Glargine (Lantus)

Eligibility Criteria

• Age: 18 Years - 65 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• For all study participants:
• Must be a male, or a female who cannot become pregnant, and who is either a healthy participant, or who has type 2 diabetes for at least 1 year
• Male participants with female partners who can become pregnant must agree to use an effective method of birth control during the study and for 4 months after study drug dosing
• Have a body mass index (BMI) of greater than 18.5 kilogram per square meter (kg/m²) and less than or equal to 35 kg/m² at screening
• Have blood pressure, pulse rate, blood and urine laboratory test results acceptable for the study
• Have venous access sufficient to allow blood sampling
• For participants with Type 2 Diabetes Mellitus (T2DM):
• Have T2DM controlled with diet and exercise alone or are stable on metformin for at least 30 days
• If taken, prescription medications for medical conditions (e.g.antihypertensive agents, aspirin or lipid lowering agents) are stable for at least 4 weeks
• Have a hemoglobin A1c (HbA1c) greater than or equal to 7.0% and less than or equal to 9.5%

You may not qualify if:

• For all study participants:
• Are currently participating in another clinical study
• Have a history of multiple and/or severe allergies to drugs or foods or a history of severe anaphylactic reaction
• Have or used to have health problems or laboratory test results or electrocardiogram (ECG) readings that, in the opinion of the doctor, could make it unsafe to participate or could interfere with understanding the results of the study
• Have donated blood or have had a loss of 500 milliliters (mL) or more in the last 3 months or have had any blood donation within the last month from screening
• Intend to start any new over-the-counter or prescription medications 7 and 14 days before planned dosing
• For participants with T2DM:
• Have taken any glucose-lowering medications, other than metformin, including insulin, in the past 3 months before screening
• Have had more than 1 episode of severe hypoglycemia, within 6 months before entry into the study, or have a history of hypoglycemia unawareness or poor recognition of hypoglycemic symptoms
• Have had a blood transfusion or severe blood loss in the past 3 months, or any blood disorder that could interfere with the understanding of the results of the study
• Have received chronic (lasting greater than 14 consecutive days) systemic glucocorticoid therapy (excluding topical, intra-articular, and inhaled preparations) in the 3 past months, or have received any glucocorticoid therapy within 30 days before screening

Sponsors & Collaborators

• Eli Lilly and Company: lead

Study Sites (1)

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri, 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST) or speak with your personal physician.

Neuss, 41460, Germany

Location

MeSH Terms

Conditions

Diabetes Mellitus, Type 2

Interventions

Insulin Glargine

Condition Hierarchy (Ancestors)

Diabetes Mellitus; Glucose Metabolism Disorders; Metabolic Diseases; Nutritional and Metabolic Diseases; Endocrine System Diseases

Intervention Hierarchy (Ancestors)

Insulin, Long-Acting; Insulins; Pancreatic Hormones; Peptide Hormones; Hormones; Hormones, Hormone Substitutes, and Hormone Antagonists; Peptides; Amino Acids, Peptides, and Proteins

Study Officials

• 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)

  Eli Lilly and Company

  STUDY DIRECTOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: DOUBLE
• Who Masked: PARTICIPANT, INVESTIGATOR
• Purpose: BASIC SCIENCE
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: October 21, 2016
• First Posted: October 24, 2016
• Study Start: December 20, 2016
• Primary Completion: October 18, 2017
• Study Completion: October 18, 2017
• Last Updated: November 7, 2017

Record last verified: 2017-11

Locations

DE (1)