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A Study of LY3437943 in Participants With Type 2 Diabetes

Phase 2
Completed
Conditions
Type 2 Diabetes
Interventions
Registration Number
NCT04867785
Lead Sponsor
Eli Lilly and Company
Brief Summary

The main purpose of this study is to evaluate the efficacy and safety of LY3437943 in participants with type 2 diabetes (T2D) who failed to achieve adequate glycemic control on diet and exercise alone or on a stable dose of metformin. This study will last about 43 weeks.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
281
Inclusion Criteria
  • Have Type 2 Diabetes (T2D)
  • Have an HbA1c value at screening of ≥7.0% and ≤10.5% and treated with diet and exercise alone or with a stable dose of metformin (either immediate release or extended release, 1000 milligram (mg)/day and not more than the locally approved dose) for at least 3 months prior to screening.
Exclusion Criteria
  • Have type 1 diabetes mellitus (T1DM)
  • Have ketoacidosis
  • Have retinopathy, maculopathy
  • Have history of pancreatitis
  • Have obesity induced by other endocrine disorders
  • Have uncontrolled hypertension
  • Have acute or chronic hepatitis
  • Have chronic kidney disease
  • Have an autoimmune abnormality for example, lupus or rheumatoid arthritis
  • Have an active or untreated malignancy

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
0.5 milligrams (mg) LY3437943LY3437943Participants received 0.5 mg LY3437943 administered as SC (subcutaneous) injection once weekly (QW).
4 mg LY3437943 (2 mg)LY3437943Participants received 2 mg LY3437943 starting dose followed by 4 mg LY3437943 administered as SC injection QW.
4 mg LY3437943 (4 mg)LY3437943Participants received 4 mg LY3437943 administered as SC injection QW.
8 mg LY3437943 (2 mg)LY3437943Participants received 2 mg LY3437943 starting dose followed by 4 mg LY3437943 and then 8 mg LY3437943 administered as SC injection QW.
12 mg LY3437943 (2 mg)LY3437943Participants received 2 mg LY3437943 starting dose followed by 4 mg LY3437943, then 8 mg LY3437943, then 12 mg LY3437943 administered as a SC injection QW.
PlaceboPlaceboParticipants received placebo administered as SC injection QW.
8 mg LY3437943 (4 mg)LY3437943Participants received 4 mg LY3437943 starting dose followed by 8 mg LY3437943 administered as a SC injection QW.
1.5 mg DulaglutideDulaglutideParticipants received 1.5 mg dulaglutide administered as SC single-dose pen injection QW.
Primary Outcome Measures
NameTimeMethod
Change From Baseline in Hemoglobin A1c (HbA1c)Baseline, 24 Weeks

Change in HbA1c (%) from baseline in LY3437943 relative to placebo. HbA1c is the glycosylated fraction of hemoglobin A. HbA1c is measured primarily to identify average plasma glucose concentration over prolonged periods of time. Least squares (LS) mean was calculated using mixed model repeated measures (MMRM) for post-baseline measures: Variable = Treatment\*Time + Strata\*Time + Baseline\*Time.

Secondary Outcome Measures
NameTimeMethod
Change From Baseline in Body WeightBaseline, 36 Weeks

Change in body weight from baseline in LY3437943 relative to placebo and dulaglutide. LSMean was calculated using MMRM for post-baseline measures: Variable = Treatment\*Time + Baseline HbA1c Group (\<=8.5%, \>8.5%)\*Time + Baseline BMI Group (\<30kg/m2, \>=30kg/m2)\*Time + Baseline\*Time.

Percentage of Participant Reaching HbA1c <7.0%Week 36

Percentage of participants reaching HbA1c \<7.0% in LY3437943 relative to placebo and dulaglutide. Estimated percentage was determined by logistic regression model with an intercept term, treatment group, baseline BMI stratum \[\<30 kg/m2, ≥30 kg/m2\] as fixed effects, and baseline HbA1c value as a covariate.

Change From Baseline in Fasting Blood Glucose (FBG)Baseline, 36 Weeks

Change in FBG from baseline in LY3437943 relative to placebo and dulaglutide. LSMean was calculated using MMRM for post-baseline measures: Variable = Treatment\*Time + Baseline HbA1c Group (\<=8.5%, \>8.5%)\*Time + Baseline BMI Group (\<30kg/m2, \>=30kg/m2)\*Time + Baseline\*Time.

Change From Baseline in HbA1cBaseline, 36 Weeks

Change in HbA1c (%) from baseline in LY3437943 relative to placebo and dulaglutide. LSMean was calculated using MMRM for post-baseline measures: Variable = Treatment\*Time + Baseline HbA1c Group (\<=8.5%, \>8.5%)\*Time + Baseline Body Mass Index (BMI) Group (\<30 kilograms/square meter (kg/m2), \>=30 kg/m2)\*Time + Baseline\*Time.

Percentage of Participants Reaching HbA1c <7.0%Week 24

Percentage of participants reaching HbA1c \<7.0% in LY3437943 relative to placebo and dulaglutide. Estimated percentage was determined by logistic regression model with an intercept term, treatment group, baseline BMI stratum \[\<30 kg/m2, ≥30 kg/m2\] as fixed effects, and baseline HbA1c value as a covariate.

Population PK: Average Steady-State Plasma Concentration (Cav,ss) of LY3437943Predose: Week 0, 1, 4, 12, 24, 30; Postdose: Week 2, 8, 16, 20, 36

The average steady-state plasma concentration of LY3437943 was evaluated using sparse sampling methodology/Population PK (PopPK) modeling.

Trial Locations

Locations (40)

Humphreys Diabetes Center

🇺🇸

Boise, Idaho, United States

Logan Health Research

🇺🇸

Kalispell, Montana, United States

Artemis Institute for Clinical Research

🇺🇸

San Diego, California, United States

Endocrine Ips, Pllc

🇺🇸

Houston, Texas, United States

Laila A Hassan, MD, PA

🇺🇸

Houston, Texas, United States

Elite Clinical Trials

🇺🇸

Rexburg, Idaho, United States

Catalina Research Institute, LLC

🇺🇸

Montclair, California, United States

Valley Endocrine, Fresno

🇺🇸

Fresno, California, United States

ForCare Clinical Research

🇺🇸

Tampa, Florida, United States

Iowa Diabetes and Endocrinology Research Center

🇺🇸

West Des Moines, Iowa, United States

San Fernando Valley Health Institute

🇺🇸

Canoga Park, California, United States

North Hills Family Medicine/North Hills Medical Research

🇺🇸

North Richland Hills, Texas, United States

Rocky Mountain Clinical Research

🇺🇸

Idaho Falls, Idaho, United States

Intend Research, LLC

🇺🇸

Norman, Oklahoma, United States

South Florida Clinical Research Institute

🇺🇸

Margate, Florida, United States

Encore Medical Research - Weston

🇺🇸

Weston, Florida, United States

Diabetes and Thyroid Center of Fort Worth

🇺🇸

Fort Worth, Texas, United States

Rainier Clinical Research Center

🇺🇸

Renton, Washington, United States

Syed Research Consultants Llc

🇺🇸

Sheffield, Alabama, United States

National Research Institute - Huntington Park

🇺🇸

Huntington Park, California, United States

Anderson Clinical Research

🇺🇸

Redlands, California, United States

National Research Institute - Panorama City

🇺🇸

Panorama City, California, United States

Diablo Clinical Research, Inc.

🇺🇸

Walnut Creek, California, United States

Lillestol Research

🇺🇸

Fargo, North Dakota, United States

MediSync Clinical Research

🇺🇸

Petal, Mississippi, United States

Cotton O'Neil Clinic

🇺🇸

Topeka, Kansas, United States

Heritage Valley Medical Group, Inc.

🇺🇸

Beaver, Pennsylvania, United States

Dallas Diabetes Research Center

🇺🇸

Dallas, Texas, United States

The Research Center of The Upstate

🇺🇸

Greenville, South Carolina, United States

National Research Institute (NRI) - Santa Ana

🇺🇸

Santa Ana, California, United States

Clinvest Research LLC

🇺🇸

Springfield, Missouri, United States

Preferred Primary Care Physicians

🇺🇸

Uniontown, Pennsylvania, United States

Southern Endocrinology Associates

🇺🇸

Mesquite, Texas, United States

The Vancouver Clinic

🇺🇸

Vancouver, Washington, United States

Frontier Clinical Research, LLC

🇺🇸

Smithfield, Pennsylvania, United States

Manati Center for Clinical Research

🇵🇷

Manati, Puerto Rico

Advanced Clinical Research, LLC

🇵🇷

Bayamon, Puerto Rico

Latin Clinical Trial Center

🇵🇷

San Juan, Puerto Rico

Universal Research Group

🇺🇸

Tacoma, Washington, United States

Centennial Medical Group

🇺🇸

Elkridge, Maryland, United States

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