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Clinical Trials in the EU / 2025-524811-35-00
Authorised, recruiting Phase III

J2A-MC-GZGY: 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

2025-524811-35-00 · tracked via the Priya Life Science EU tracker
Sponsor
Eli Lilly & Co
Sponsor type
Pharmaceutical company
Therapeutic area
Nutritional and Metabolic Diseases
Decision date
22/09/2026
Enrollment target
22
Sites
Italy, Spain, Belgium

Condition studied

Diabetes Mellitus, Type 2

Investigational medicinal product(s)

ORFORGLIPRONOrforglipronDULAGLUTIDE

Every trial of Dulaglutide and Orforglipron across our registers →

Eligibility

Age group
0-17 years
Sex
Female, Male

Primary endpoint

Change from Baseline in Hemoglobin A1c (HbA1c)

Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2025-524811-35-00 on CTIS ↗ ← All trials in the EU