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Recruiting Phase 2 NCT07215312

A Study of LY3938577 in Participants With Type 2 Diabetes Previously Treated With Basal Insulin

Phase 2 – studying effectiveness and dosage
Conditions: Diabetes Mellitus, Type 2

Sponsor: Eli Lilly and Company

trial.available_in: БГ
Overview
The purpose of this study is to see how well LY3938577 works and how safe it is compared to degludec in people with type 2 diabetes. Participation in the study will last about 26 weeks.
Who can participate
Inclusion Criteria: * Have type 2 diabetes * Are receiving ≥20 units of basal insulin per day and ≤55 units/day and ≤1.5 units/kg/day at screening * Have hemoglobin A1c (HbA1c) 7.5% to 10.5% inclusive * Have a body mass index (BMI) of 20 or higher and less than 35 kilograms per square meter (kg/m2) Exclusion Criteria: * Have type 1 diabetes
Interventions
LY3938577
DRUG
Degludec
DRUG
Locations 26
Argentina (6)
Cicemo Srl
Buenos Aires
CIPREC
Buenos Aires
Mautalen Salud e Investigación
Buenos Aires
Centro Medico Dra. Laura Maffei- Investigacion Clinica Aplicada
Buenos Aires
Instituto Centenario
CABA
Instituto Médico Catamarca IMEC
Rosario
United States (20)
Texas Diabetes & Endocrinology, P.A.
Austin , Texas
Holston Medical Group
Bristol , Tennessee
Tampa Bay Medical Research
Clearwater , Florida
Velocity Clinical Research, Dallas
Dallas , Texas
Tribe Clinical Research, LLC
Greenville , South Carolina
Encore Medical Research
Hollywood , Florida
Juno Research
Houston , Texas
Clinical Research of Central Florida
Lakeland , Florida
Southern Endocrinology Associates
Mesquite , Texas
AMR Clinical
Norman , Oklahoma
Consano Clinical Research, LLC
Shavano Park , Texas
Encompass Clinical Research
Spring Valley , California
Washington University School of Medicine
St Louis , Missouri
Chrysalis Clinical Research
St. George , Utah
Tucson Clinical Research Institute
Tucson , Arizona
University Clinical Investigators, Inc.
Tustin , California
Texas Valley Clinical Research
Weslaco , Texas
Iowa Diabetes and Endocrinology Research Center
West Des Moines , Iowa
Encore Medical Research - Weston
Weston , Florida
Accellacare - Wilmington
Wilmington , North Carolina
Technical details
Status
Recruiting
Phase
Phase 2
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Maximum age
70 Years
Healthy volunteers
No
Start date
13.10.2025
Completion date
01.12.2026
Registry ID
NCT07215312
Source
clinicaltrials.gov
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Information is automatically extracted from ClinicalTrials.gov. Consult your doctor before taking action.