A Master Protocol Study (LY900038) of Multiple Intervention-Specific-Appendices (ISAs) in Adult Participants With Obesity or Overweight
Eli Lilly and Company · NCT06143956
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–75 · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Phase 2
- Target enrollment
- 1481
- US sites recruiting
- 43
- Study start
- November 17, 2023
- Record last updated
- October 7, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The purpose of this Phase-2 chronic weight management master protocol (CWMM) is to create a framework to evaluate the safety and efficacy of various investigational interventions for chronic weight management with intervention-specific appendices (ISAs). The CWMM establishes entry criteria for newly enrolled participants across the master and the ISAs. The ISAs may start independently of other ISAs as interventions become available for clinical testing. The results for the CWMM screening record will be reported when all the ISA's complete.
Being studied: LY3305677; LY3841136; Tirzepatide; LY3549492; LY3532226; Placebo; Placebo
Conditions: Obesity; Overweight
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Have a body mass index (BMI)
- ≥30 kilogram/square meter (kg/m²), or
- ≥27 kg/m² and \<30 kg/m², or with at least 1 weight-related comorbidity
- Have had a stable body weight for the 3 months prior to randomization (\<5%) body weight gain and/or loss.
Exclusion Criteria
- Have a prior or planned surgical treatment for obesity, except prior liposuction or abdominoplasty, if performed >1 year prior to screening.
- Have type 1 diabetes mellitus, latent autoimmune diabetes in adults, or history of ketoacidosis or hyperosmolar coma.
- Have poorly controlled hypertension.
- Have signs and symptoms of any liver disease other than nonalcoholic fatty liver disease.
- 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 symptomatic gallbladder disease within the past 2 years.
- Have a lifetime history of suicide attempts.
Recruiting US locations
The Institute for Liver Health II dba Arizona Clinical Trials - Mesa
Chandler, AZ 85225
Site contact: Yessica Sachdeva
Headlands Research - Scottsdale
Scottsdale, AZ 85260
Site contact: 480-725-8708
The Institute for Liver Health II dba Arizona Liver Health-Tucson
Tucson, AZ 85712
Site contact: 480-470-4000
NorCal Medical Research, Inc
Greenbrae, CA 94904
Site contact: 415-461-1585
Velocity Clinical Research, Huntington Park
Huntington Park, CA 90255
Site contact: 323-588-1990
Peninsula Research Associates
Rolling Hills Estates, CA 90274
Site contact: 310-265-1623
Diablo Clinical Research, Inc.
Walnut Creek, CA 94598
Site contact: 925-930-7267
Stamford Therapeutics Consortium
Stamford, CT 06905
Site contact: David Radin
New Horizon Research Center
Miami, FL 33165
Site contact: 305-226-3933
Indago Research & Health Center, Inc
Miami Lakes, FL 33016
Site contact: 305-825-6588
Suncoast Clinical Research, Inc.
New Port Richey, FL 34652
Site contact: 727-849-4131
Charter Research - Winter Park
Orlando, FL 32803
Site contact: 407-337-3000
Charter Research - Lady Lake
The Villages, FL 32162
Site contact: 352-441-2000
Medical Research Partners
Ammon, ID 83406
Site contact: 208-681-9070
Great Lakes Clinical Trials - Ravenswood
Chicago, IL 60640
Site contact: 773-275-3500 Ext 162
Iowa Diabetes and Endocrinology Research Center
West Des Moines, IA 50266
Site contact: 515-329-6800
Cotton O'Neil Diabetes & Endocrinology
Topeka, KS 66606
Site contact: 785-354-9591
Monroe Biomedical Research - Louisville
Louisville, KY 40213
Site contact: 502-515-5672
Knownwell
Needham, MA 02492
Site contact: 339-793-8998
Lucida Clinical Trials
New Bedford, MA 02740
Site contact: 508-720-2015
Headlands Research - Detroit
Southfield, MI 48034
Site contact: Christopher Romero
Arcturus Healthcare , PLC, Troy Internal Medicine Research Division
Troy, MI 48098
Site contact: 248-312-0025
StudyMetrix Research
City of Saint Peters, MO 63303
Site contact: 636-387-5100
Clinvest Headlands Llc
Springfield, MO 65807
Site contact: Christina Capps
Las Vegas Medical Research
Las Vegas, NV 89128
Site contact: 702-750-0000
Dent Neurologic Institute
Amherst, NY 14226
Site contact: Laszlo Mechtler
Velocity Clinical Research, Syracuse
East Syracuse, NY 13057
Site contact: Rachel Dubroff
Rochester Clinical Research, LLC
Rochester, NY 14609
Site contact: 585-288-0890
Medication Management
Greensboro, NC 27401
Site contact: 336-763-6968
Monroe Biomedical Research
Monroe, NC 28112
Site contact: 704-283-7359
Lucas Research, Inc
Morehead City, NC 28557
Site contact: 252-222-5700
Lucas Research, Inc.
New Bern, NC 28562
Site contact: 252-649-1944
CTI Clinical Research Center
Cincinnati, OH 45212
Site contact: 513-721-3868
Tribe Clinical Research, LLC
Greenville, SC 29607
Site contact: 864-334-0141
Quality Medical Research
Nashville, TN 37211
Site contact: 615-835-4750
IMA Clinical Research Austin
Austin, TX 78745
Site contact: 512-649-0082
Velocity Clinical Research, Dallas
Dallas, TX 75230
Site contact: Dan Lender
FutureSearch Trials of Dallas
Dallas, TX 75251
Site contact: 214-369-2600
PlanIt Research, PLLC
Houston, TX 77079
Site contact: 713-973-3415
Endeavor Clinical Trials
San Antonio, TX 78240
Site contact: 518-428-6859
Texas Valley Clinical Research
Weslaco, TX 78596
Site contact: 956-431-8090
Sovah Clinical Research-River District
Danville, VA 24541
Site contact: 434-793-4711
Central Washington Health Services Association d/b/a Confluence Health
Wenatchee, WA 98801
Site contact: 509-436-4050
Study contacts (from the official record)
- Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or · 1-317-615-4559 · LillyTrials@Lilly.com
- Physicians interested in becoming principal investigators please contact · clinical_inquiry_hub@lilly.com
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