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Clinical Trial Details

Trial ID: L3307
Source ID: NCT06362265
Associated Drug: Ly3209590
Title: A Study to Evaluate Pharmacokinetics of LY3209590 in Pediatric Participants With Type 2 Diabetes Mellitus
Acronym:
Status: RECRUITING
Study Results: NO
Results:
Conditions: Type 2 Diabetes Mellitus
Interventions: DRUG: LY3209590
Outcome Measures: Primary: Pharmacokinetics (PK): Area Under the Plasma Concentration Versus Time Curve (AUC) of LY3209590, Predose up to 65 days post dose|PK: Maximum Observed Plasma Concentration (Cmax) of LY3209590, Predose up to 65 days post dose | Secondary: Change from Baseline in Fasting Glucose, Baseline, 65 days
Sponsor/Collaborators: Sponsor: Eli Lilly and Company
Gender: ALL
Age: CHILD
Phases: PHASE1
Enrollment: 22
Study Type: INTERVENTIONAL
Study Designs: Allocation: NON_RANDOMIZED|Intervention Model: SINGLE_GROUP|Masking: NONE|Primary Purpose: BASIC_SCIENCE
Start Date: 2024-10-10
Completion Date: 2026-11
Results First Posted:
Last Update Posted: 2025-03-28
Locations: Honor Health Research Institute, Scottsdale, Arizona, 85258, United States|Children's Hospital Los Angeles, Los Angeles, California, 90027, United States|Children's Healthcare of Atlanta - Center for Advanced Pediatrics, Atlanta, Georgia, 30329, United States|Centricity Research Columbus Endocrinology, Columbus, Georgia, 31904, United States|Johns Hopkins Hospital, Baltimore, Maryland, 21287, United States|Joslin Diabetes Center, Boston, Massachusetts, 02215, United States|UBMD Pediatrics, Buffalo, New York, 14203, United States|NYU Langone, New York, New York, 10016, United States|Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, 45229-3039, United States|Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, 19104, United States|Lifedoc Research - Lenox Park Drive, Memphis, Tennessee, 38115, United States
URL: https://clinicaltrials.gov/show/NCT06362265