A Study of Macupatide (LY3532226) and Eloralintide (LY3841136), Alone or in Combination, in Adults With Obesity or Overweight and With Type 2 Diabetes
Sponsored by Eli Lilly and Company
About this study
The purpose of this study is to investigate weight reduction with macupatide and eloralintide, alone or in combination, in adult participants with obesity or overweight and with type 2 diabetes. Participation in the study will last about 48 weeks.
Where this study is enrolling (22)
- Call +1 602-200-3814
Synexus Clinical Research US, Inc.
Phoenix, Arizona
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- Call 520-838-3540
Pima Heart
Tucson, Arizona
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- I'm interested
Prime Medical Group, LLC dba Gilbert Center for Family Medicine, LLC
Gilbert, Arizona
- I'm interested
AGILE Clinical Research Trials, LLC
Sandy Springs, Georgia
- I'm interested
SKY Clinical Research Network Group-Brown
Atlanta, Georgia
Show all 22 locations
- Call 678-825-2887
Pivotal Research Solutions
Stonecrest, Georgia
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- Call 470-317-3604
Rophe Adult and Pediatric Medicine/SKYCRNG
Union City, Georgia
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- Call 702-750-0000
Vector Clinical Trials
Las Vegas, Nevada
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- Call 609-392-6666
Premier Research
Trenton, New Jersey
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- Call 937-534-4201
PriMED Clinical Research
Dayton, Ohio
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- I'm interested
Biopharma Informatic, LLC
Houston, Texas
- Call 210-545-4900
Consano Clinical Research, LLC
Shavano Park, Texas
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- Call 281-944-3610
Mercy Family Clinic
Dallas, Texas
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- I'm interested
PlanIt Research, PLLC
Houston, Texas
- Call 281-944-3610
Research Physicians Network, LLC
Houston, Texas
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- Call 956-431-8090
Texas Valley Clinical Research
Weslaco, Texas
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- Call 713-282-5600
Aavon Clinical Trials
Richmond, Texas
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- Call 801-363-7353
Kalo Clinical Research
West Valley City, Utah
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- Call 757-446-5291
Eastern Virginia Medical School (EVMS) Medical Group
Norfolk, Virginia
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- Call 804-477-3045
Clinical Research Partners, LLC
Richmond, Virginia
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- Call 253-882-1070
Universal Research Group
Tacoma, Washington
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- Call 425-251-1720
Rainier Clinical Research Center
Renton, Washington
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Who can participate
Inclusion criteria
- ✓Have type 2 diabetes
- ✓Have an HbA1c ≥7.5% to ≤10.5% at screening
- ✓Have been treated with any of the following, alone or in combination, for at least 3 months prior to screening
- ✓Diet and exercise
- ✓Stable dose of metformin
- ✓Sodium-glucose cotransporter-2 (SGLT2) inhibitor
- ✓Have had a stable body weight (\<5% body weight gain and/or loss) for the 3 months prior to screening
- ✓Have a BMI of 27 or greater at screening
Exclusion criteria
- ✕Have any form of diabetes other than type 2 diabetes
- ✕Have a prior or planned surgical treatment for obesity, except prior liposuction or abdominoplasty, if performed \>1 year prior to screening
- ✕Have any of the following cardiovascular conditions within 3 months prior to screening:
- ✕acute myocardial infarction
- ✕cerebrovascular accident (stroke)
- ✕unstable angina, or
- ✕hospitalization due to congestive heart failure
- ✕Have a history of an active or untreated malignancy or are in remission from a clinically significant malignancy for less than 5 years, exceptions include
- ✕basal or squamous cell skin cancer
- ✕in situ carcinomas of the cervix, or
- ✕in situ prostate cancer
- ✕Have been prescribed any of the following receptor agonists (RA) or their combination for any indication within the last 6 months:
- ✕amylin RA
- ✕dual amylin and calcitonin RA
- ✕glucagon-like peptide-1 receptor (GLP-1) RA
- ✕glucose-dependent insulinotropic peptide (GIP)/GLP-1 RA
- ✕GLP-1/glucagon (GCG) RAs, or
- ✕GIP/GLP-1/GCG RAs
- ✕Have used excluded antihyperglycemic medications within 3 months prior to screening (including, but not limited to, sulfonylureas, dipeptidyl peptidase-4 inhibitors, alpha-glucosidase inhibitors, thiazolidinediones, and meglitinides
- ✕Have used insulin for diabetic control within the prior year (short term use in certain situations allowed
Only the research team can confirm whether you qualify. The intake questionnaire is the best way to find out.
Completing a questionnaire on Clinably does not enroll you in a clinical trial or confirm your eligibility. Only the research team can determine whether you qualify to participate. These results are based on the information you provide and are intended to help you start a conversation with the research team.
Trial data sourced from ClinicalTrials.gov.