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Not yet recruiting Phase 3 Interventional

A Study of Orforglipron (LY3502970) Compared With Dulaglutide in Pediatric Participants With Type 2 Diabetes

ClinicalTrials.gov ID: NCT07668336

Public ClinicalTrials.gov record NCT07668336. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 23, 2026, 10:43 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3, Randomized, Open-Label Study to Investigate the Efficacy, Safety, and Pharmacokinetics of Once-Daily Oral Orforglipron Compared With Once-Weekly Dulaglutide in Pediatric Participants 10 to Less Than 18 Years of Age With Type 2 Diabetes

Study identification

NCT ID
NCT07668336
Recruitment status
Not yet recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Eli Lilly and Company
Industry
Enrollment
170 participants

Conditions and interventions

Interventions

  • Orforglipron Drug
  • Dulaglutide Drug

Drug

Eligibility (public fields only)

Age range
10 Years to 17 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 31, 2026
Primary completion
Feb 28, 2030
Completion
Feb 28, 2030
Last update posted
Jul 19, 2026

2026 – 2030

United States locations

U.S. sites
17
U.S. states
10
U.S. cities
17
Facility City State ZIP Site status
Sutter Valley Medical Foundation (SVMF) Pediatric Endocrinology Sacramento California 95821
Rady Children's Hospital San Diego California 92123
Stamford Therapeutics Consortium Stamford Connecticut 06905
Children's Healthcare of Atlanta - Center for Advanced Pediatrics (CAP) Atlanta Georgia 30329
CenExel iResearch, LLC Decatur Georgia 30030
Medical Research Partners Ammon Idaho 83406
Cotton O'Neil Diabetes & Endocrinology Topeka Kansas 66606
SUNY Upstate Medical University Syracuse New York 13210
Advantage Clinical Trials The Bronx New York 10467
Central States Research Tulsa Oklahoma 74136
Frontier Clinical Research, LLC Smithfield Pennsylvania 15478
Vanderbilt Health One Hundred Oaks Nashville Tennessee 37204
Gadolin Research Beaumont Texas 77702
Driscoll Children's Hospital Corpus Christi Texas 78411
Proactive Clinical Research LLC Edinburg Texas 78539
Consano Clinical Research, LLC Shavano Park Texas 78231
Victoria Clinical Research Group Victoria Texas 77901

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 54 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07668336, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 19, 2026 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07668336 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →