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Phase 3Recruiting

A Study of Dulaglutide (LY2189265) 3.0 mg and 4.5 mg in Pediatric Participants With Type 2 Diabetes Mellitus (AWARD-PEDS PLUS)

Sponsored by Eli Lilly and Company

About this study

The main purpose of this study is to evaluate additional dosing options for dulaglutide in pediatric participants with Type 2 Diabetes. Participation in this study will last about 8 months.

Where this study is enrolling (35)

  • University of Arizona

    Tucson, Arizona

    I'm interested

  • Arkansas Childrens Hospital

    Little Rock, Arkansas

    Call 505-272-5551

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  • UCLA Mattel Children's Hospital

    Los Angeles, California

    Call 310-203-7631

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  • University of California, San Francisco

    San Francisco, California

    Call 415-514-6234

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  • Children's Hospital of Colorado

    Denver, Colorado

    Call 20-777-3618

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Show all 35 locations

  • Yale Diabetes Research

    New Haven, Connecticut

    Call 203-737-7177

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  • Children's National Medical Center

    Washington D.C., District of Columbia

    Call 888-884-2327

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  • Emerson Clinical Research Institute

    Washington D.C., District of Columbia

    Call 202-239-0777

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  • D&H National Research Centers, Inc

    Miami, Florida

    Call 786-375-6210

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  • AdventHealth Orlando

    Orlando, Florida

    Call 407-896-2901

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  • D&H Tamarac Research Center, LLC

    Tamarac, Florida

    Call 786-375-6210

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  • Children's Healthcare of Atlanta - Center for Advanced Pediatrics

    Atlanta, Georgia

    Call 404-256-2593

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  • St. Luke's Children's Endocrinology and Diabetes

    Boise, Idaho

    Call 208-381-7340

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  • University of Illinois at Chicago

    Chicago, Illinois

    Call 312-307-9385

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  • Center for Diabetes and Metabolic Diseases Indiana University

    Indianapolis, Indiana

    Call 317-278-9699

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  • University of Iowa Stead Family Children's Hospitals

    Iowa City, Iowa

    Call 319-335-0077

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  • Norton Children's Endocrinology

    Louisville, Kentucky

    Call 502-588-3400

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  • Johns Hopkins University School of Medicine

    Baltimore, Maryland

    Call 443-287-9032

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  • University of Mississippi Medical Center

    Jackson, Mississippi

    Call 601-815-5000

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  • University of New Mexico Hospital

    Albuquerque, New Mexico

    Call 505-272-3073

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  • SUNY Upstate Medical University

    Syracuse, New York

    Call 315-464-9006

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  • Cohen Children's Medical Center Division of Pediatric Endocrinology

    Hyde Park, New York

    Call 516-472-3750

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  • UNC Children's Hospital

    Chapel Hill, North Carolina

    Call 919-966-2333

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  • Childrens Hospital Medical Center

    Cincinnati, Ohio

    Call 513-803-7274

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  • Cleveland Clinic Childrens Outpatient Center

    Cleveland, Ohio

    Call 216-636-2828

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  • University of Oklahoma Health Sciences Center

    Oklahoma City, Oklahoma

    Call 405-271-6764

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  • St Christophers Hospital For Children

    Philadelphia, Pennsylvania

    I'm interested

  • Children's Hospital of Philadelphia

    Philadelphia, Pennsylvania

    Call 800-879-2467

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  • Prisma Health Pediatric Endocrinology

    Columbia, South Carolina

    Call 803-434-7990

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  • Prisma Health Midlands

    Greenville, South Carolina

    Call 864-454-5656

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  • Texas Childrens Hospital

    Houston, Texas

    I'm interested

  • Research Institute of Dallas

    Dallas, Texas

    Call 248-817-4331

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  • UT Health Houston

    Houston, Texas

    Call 713-500-7257

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  • Seattle Children's Hospital

    Seattle, Washington

    Call 206-987-3897

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  • Children's Wisconsin - Milwaukee Campus

    Milwaukee, Wisconsin

    Call 414-955-8486

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Who can participate

Inclusion criteria

  • ✓Have Type 2 diabetes treated with diet and exercise and metformin and/or basal insulin. Metformin and/or basal insulin dose must be stable for at least 8 weeks prior to screening.
  • ✓Have a body weight ≥50 kilograms (kg) and Body Mass Index (BMI) of \>85th percentile

Exclusion criteria

  • ✕Have Type 1 diabetes
  • ✕Have received treatment with any glucose-lowering agent(s) other than metformin, basal insulin, or dulaglutide within 8 weeks prior to screening
  • ✕After the Type 2 diabetes diagnosis, have a history of diabetic ketoacidosis or hyperosmolar syndrome
  • ✕Have had ≥1 episode of severe hypoglycemia and/or ≥1 episode of hypoglycemic unawareness within the last 6 months
  • ✕Have family or personal history of medullary thyroid carcinoma (MTC) or multiple endocrine neoplasia syndrome type 2 (MEN2)
  • ✕Have prior chronic, recurrent, or idiopathic pancreatitis, or known gallbladder disease
  • ✕Have been treated with prescription drugs or over-the-counter medications that promote weight loss within 8 weeks prior to screening

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.