Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING Phase 3

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

NCT06739122 · View on ClinicalTrials.gov ↗

Study Summary

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.

Conditions Studied

Interventions

  • DRUG Dulaglutide

Study Locations (20)

Florida

  • Nemours Children's Health — Jacksonville
  • D&H National Research Centers, Inc — Miami
  • AdventHealth Orlando — Orlando
  • D&H Tamarac Research Center, LLC — Tamarac
  • University of South Florida — Tampa

California

  • Division of Endocrinology, Diabetes, and Metabolism — Los Angeles
  • UCLA Mattel Children's Hospital — Los Angeles
  • University of California, San Francisco — San Francisco

District of Columbia

  • Emerson Clinical Research Institute — Washington D.C.
  • Children's National Medical Center — Washington D.C.

Georgia

  • Children's Healthcare of Atlanta - Center for Advanced Pediatrics — Atlanta
  • Centricity Research Columbus Endocrinology — Columbus

Arizona

  • University of Arizona — Tucson

Arkansas

  • Arkansas Childrens Hospital — Little Rock

Colorado

  • Children's Hospital of Colorado — Denver

Connecticut

  • Yale Diabetes Research — New Haven

Trial Details

FieldValue
Enrollment Target 55 participants
Start Date 2025-01-10
Est. Completion 2027-12
Phase Phase 3

Sponsor

Eli Lilly and Company

704 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06739122

The ClinicalTrials.gov registry entry for NCT06739122 describes a study currently listed as recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 55 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Eli Lilly and Company, which has 704 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Type 2 Diabetes appearing as the primary indexed condition, and to 1 intervention — of which Dulaglutide is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06739122 reports 20 study locations spanning 12 distinct geographic areas — top geographies include Florida, California, District of Columbia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06739122 about?

NCT06739122 is a clinical study titled "A Study of Dulaglutide (LY2189265) 3.0 mg and 4.5 mg in Pediatric Participants With Type 2 Diabetes Mellitus (AWARD-PEDS PLUS)". 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.

What is the current status of trial NCT06739122?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 55 participants. The study started on 2025-01-10. Estimated completion is 2027-12.

What conditions does trial NCT06739122 study?

This clinical trial studies the following conditions: Type 2 Diabetes. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06739122?

The interventions under investigation include: Dulaglutide (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06739122?

This trial is sponsored by Eli Lilly and Company, which has 704 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06739122 being conducted?

This trial has 20 study locations across Arizona, Arkansas, California, Colorado, Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial