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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06045221
Other study ID # 18565
Secondary ID J2A-MC-GZGUU1111
Status Recruiting
Phase Phase 3
First received
Last updated
Start date September 22, 2023
Est. completion date July 25, 2025

Study information

Verified date June 1, 2024
Source Eli Lilly and Company
Contact There may be multiple sites in this clinical trial. 1-877-CTLILL
Phone 1-317-615-4559
Email ClinicalTrials.gov@lilly.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The main purpose of this study is to assess efficacy and safety of orforglipron compared with oral semaglutide in participants with Type 2 diabetes and inadequate glycemic control with metformin.The study will last around 61 weeks.


Recruitment information / eligibility

Status Recruiting
Enrollment 1576
Est. completion date July 25, 2025
Est. primary completion date July 25, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Have Type 2 Diabetes - Have HbA1c =7.0% (53 mmol/mol) to =10.5% (91 mmol/mol), as determined by the central laboratory at screening. - Have been on stable diabetes treatment with metformin =1500 milligram (mg)/day during the 90 days prior to screening and maintained through randomization. - Are of stable body weight (±5%) for at least 90 days prior to screening and agree to not initiate an intensive diet or exercise program during the study with the intent of reducing body weight, other than the lifestyle and/or dietary measures for diabetes treatment Exclusion Criteria: - Have Type 1 Diabetes - Are currently receiving or planning to receive treatment for diabetic retinopathy and/or macular edema, for example, laser photocoagulation or intravitreal injections of anti-vascular endothelial growth factor inhibitors. - Have a history of ketoacidosis or hyperosmolar state or coma within the last 6 months prior to screening, or between screening and randomization. - Have a New York Heart Association functional classification IV congestive heart failure. - Have an estimated glomerular filtration rate (eGFR) <45 milliliter/minute (mL/min)/1.73 square meter (m²) or lower than the country-specific threshold for discontinuing metformin therapy per local label as determined by the central laboratory at screening. - Have a serum calcitonin level of =35 nanogram/Liter (ng/L), as determined by the central laboratory at screening. - Have a history of an active or untreated malignancy or are in remission from a clinically significant malignancy for less than 5 years.

Study Design


Intervention

Drug:
Orforglipron
Administered orally
Semaglutide
Administered orally

Locations

Country Name City State
Argentina Centro Médico Viamonte Buenos Aires Ciudad Autónoma De Buenos Aires
Argentina CIPREC Buenos Aires Ciudad Autónoma De Buenos Aires
Argentina Instituto Centenario Caba Ciudad Autónoma De Buenos Aires
Argentina Consultorio de Investigación Clínica EMO SRL Ciudad Autonoma de Buenos Aires Ciudad Autónoma De Buenos Aires
Argentina Centro de Investigaciones Metabólicas (CINME) Ciudad Autónoma de Buenos Aires Buenos Aires
Argentina Instituto de Investigaciones Clínicas Córdoba Córdoba
Argentina Instituto Médico DAMIC Córdoba
Argentina CIMeL Clinical Research Lanus Buenos Aires
Argentina Centro de Investigaciones Médicas Mar del Plata Mar del Plata Buenos Aires
Argentina Policlinica Red OMIP Mar del Plata Buenos Aires
Argentina Fundacion Estudios Clinicos Rosario Santa Fe
Argentina INECO Neurociencias Oroño Rosario Santa Fe
Argentina Instituto de Especialidades de la Salud Rosario Rosario Santa Fe
Argentina Instituto Médico Catamarca IMEC Rosario Santa Fe
Argentina Instituto Médico Fundación Grupo Colaborativo Rosario Investigación y Prevención Medica Rosario Santa Fe
Argentina Centro de Salud e Investigaciones Médicas Santa Rosa La Pampa
Argentina Sanatorio Norte Santiago del Estero
China Beijing Pinggu District Hospital Beijing Beijing
China West China Hospital of Sichuan University ChengDu Sichuan
China Chongqing General Hospital Chongqing Chongqing
China Dalian Municipal Central Hospital Affiliated of Dalian Medical University Dalian Liaoning
China Shunde Hospital of Southern Medical Univesity Foshan Guangdong
China Zhejiang Hospital Hangzhou Zhejiang
China The Fourth Hospital of Harbin Medical University Harbin Heilongjiang
China Huizhou Municipal Central Hospital Huizhou Guangdong
China Huzhou Central Hospital Huzhou Zhejiang
China Jinan Central Hospital Jinan Shandong
China First Affiliated Hospital of Kunming Medical University Kunming Yunnan
China The First Affiliated Hospital of Henan University of Science &Technology Luoyang Shi Henan
China Nanjing First Hospital Nanjing Jiangsu
China The Second Affiliated Hospital of Nanjing Medical University Nanjing Jiangsu
China Nanyang First People's Hospital Nanyang Henan
China Jiangxi Pingxiang People's Hospital Pingxiang Jiangxi
China Pudong New Area People's Hospital Shanghai Shanghai Shanghai
China Shanghai Sixth People's Hospital Shanghai Shanghai
China The First Affiliated Hospital of Wenzhou Medical University Wenzhou Zhejiang
China The Second Affiliated Hospital of Zhengzhou University Zhengzhou Henan
China Affiliated Hospital of Jiangsu University Zhenjiang Jiangsu
Japan Gifu University Hospital Gifu
Japan Takai Internal Medicine Clinic Kamakura-shi Kanagawa
Japan Shiraiwa Medical Clinic Kashiwara Osaka
Japan Mikannohana Clinic, Diabetes, Endocrinology and Metabolism Matsuyama Ehime
Japan Nakamoto Internal Medicine Clinic Mito Ibaraki
Japan Nakakinen clinic Naka Ibaraki
Japan Medical Corporation Sato Medical clinic Ootaku Tokyo
Japan Manda Memorial Hospital Sapporo Hokkaido
Japan Ohishi Internal Medicine Clinic Tsuchiura Ibaraki
Mexico Centro Para El Desarrollo de La Medicina Y de Asistencia Medica Especializada S.C. Culiacan Sinaloa
Mexico Lahoja. Asociacion Para La Investigacion Y La Farmacovigilancia Durango
Mexico Centro de Investigacion Medica Integral Guadalajara Jalisco
Mexico CICEJ Centro de Investigación Clínica Endocrinológica de Jalisco S.C Guadalajara Jalisco
Mexico Consultorio Médico Guadalajara Jalisco
Mexico Instituto Jalisciense de Investigacion en Diabetes y Obesidad Guadalajara Jalisco
Mexico Private Practice - Dr. Arechavaleta Granell Maria del Rosario Guadalajara Jalisco
Mexico Virgen Cardiovascular Research SC Guadalajara Jalisco
Mexico CAIMED México Mexico City Distrito Federal
Mexico Centro Especializado En Diabetes, Obesidad Y Prevencion De Enfermedades Cardiovasculares Mexico City Distrito Federal
Mexico Cardiolink Clin Trials Monterrey Nuevo León
Mexico Clínica García Flores SC Monterrey Nuevo León
Mexico Eukarya PharmaSite Monterrey Nuevo León
Mexico Hospital Universitario "Dr. Jose Eleuterio Gonzalez" Monterrey Nuevo León
Mexico Unidad biomedica avanzada monterrey Monterrey Nuevo León
Mexico Centro de investigación y control metabólico San Nicolás de los Garza Nuevo León
Mexico Centro de Investigacion Medica de Occidente, S.C. Zapopan Jalisco
Puerto Rico Private Practice - Dr. Paola Mansilla-Letelier Guaynabo
Puerto Rico Research and Cardiovascular Corp. Ponce
Puerto Rico Endocrinologist Metabolic Clinic & Research Institute San Juan
Puerto Rico Latin Clinical Trial Center San Juan
United States Albany Medical College, Division of Community Endocrinology Albany New York
United States Velocity Clinical Research, Austin Austin Texas
United States Heritage Valley Medical Group, Inc. Beaver Pennsylvania
United States Northwest Clinical Trials Boise Idaho
United States Joslin Diabetes Center Boston Massachusetts
United States Ellipsis Research Group Brooklyn New York
United States San Fernando Valley Health Institute Canoga Park California
United States Clinical Research of West Florida, Inc. (Clearwater) Clearwater Florida
United States Aventiv Research Inc Columbus Ohio
United States The Corvallis Clinic, P.C. Corvallis Oregon
United States Connecticut Clinical Research - Cromwell Cromwell Connecticut
United States Dallas Diabetes Research Center Dallas Texas
United States Revival Research Institute - Dearborn Dearborn Michigan
United States Neighborhood Healthcare Institute of Health Escondido California
United States Diabetes and Thyroid Center of Ft. Worth Fort Worth Texas
United States Velocity Clinical Research, Gardena Gardena California
United States New West Physicians Clinical Research Golden Colorado
United States American Health Network of IN, LLC Greenfield Indiana
United States PharmQuest Greensboro North Carolina
United States The Research Center of The Upstate Greenville South Carolina
United States Clear Brook Medical Associates Houston Texas
United States Endocrine Ips, Pllc Houston Texas
United States Juno Research Houston Texas
United States Family First Medical Center Idaho Falls Idaho
United States Glacier View Research Institute - Endocrinology Kalispell Montana
United States Kansas City Research Institute Kansas City Missouri
United States New Phase Research and Development Knoxville Tennessee
United States Wr-Crcn, Llc Las Vegas Nevada
United States Balanced Life Health Care Solutions/SKYCRNG Lawrenceville Georgia
United States Biopharma Informatic Los Angeles California
United States National Research Institute - Wilshire Los Angeles California
United States South Florida Clinical Research Institute Margate Florida
United States Clinical Neuroscience Solutions, Inc. dba CNS Healthcare Memphis Tennessee
United States Southern Endocrinology Associates Mesquite Texas
United States Miami Dade Medical Research Institute, LLC Miami Florida
United States Tekton Research, Inc Moore Oklahoma
United States Lucas Research, Inc Morehead City North Carolina
United States DelRicht Research New Orleans Louisiana
United States Infinity Clinical Research - Norco Norco California
United States Intend Research, LLC Norman Oklahoma
United States Valley Clinical Trials, Inc. Northridge California
United States West Orange Endocrinology Ocoee Florida
United States Absolute Clinical Research Phoenix Arizona
United States Office 18 Pittsburgh Pennsylvania
United States Eastside Research Associates Redmond Washington
United States Rainier Clinical Research Center Renton Washington
United States SKY Clinical Research Network Group-Quinn Ridgeland Mississippi
United States Synexus Clinical Research US, Inc. Salt Lake City Utah
United States Norcal Endocrinology & Internal Medicine San Ramon California
United States Encompass Clinical Research Spring Valley California
United States Accellacare - Piedmont Statesville North Carolina
United States Clinical Research Atlanta Stockbridge Georgia
United States Latin Clinical Trial Center Florida Tamarac Florida
United States Clinical Research of West Florida Tampa Florida
United States Cotton O'Neil Clinical Research Center Topeka Kansas
United States Premier Research Trenton New Jersey
United States University Clinical Investigators, Inc. Tustin California
United States Velocity Clinical Research, Valparaiso Valparaiso Indiana
United States Texas Valley Clinical Research Weslaco Texas
United States Metabolic Research Institute, Inc. West Palm Beach Florida
United States Great Lakes Medical Research, LLC Westfield New York
United States Tekton Research - Wichita Wichita Kansas
United States Wake Forest University Baptist Medical Center (WFUBMC) Winston-Salem North Carolina
United States North Georgia Clinical Research Woodstock Georgia

Sponsors (1)

Lead Sponsor Collaborator
Eli Lilly and Company

Countries where clinical trial is conducted

United States,  Argentina,  China,  Japan,  Mexico,  Puerto Rico, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from Baseline in Hemoglobin A1c (HbA1c) Baseline, Week 52
Secondary Change from Baseline in HbA1c Baseline, Week 52
Secondary Percentage of Participants Who Achieved HbA1c <7.0% 53 millimole/mole (mmol/mol) Week 52
Secondary Percentage of Participants Who Achieved HbA1c =6.5% (48 mmol/mol) Week 52
Secondary Percentage Change from Baseline in Body Weight Baseline, Week 52
Secondary Change from Baseline in Body Weight Baseline, Week 52
Secondary Percentage of Participants Who Achieved HbA1c <5.7% (39 mmol/mol) Week 52
Secondary Change from Baseline in Fasting Serum Glucose Baseline, Week 52
Secondary Change from Baseline in Daily Average 7-point Self-monitored Blood Glucose (SMBG) Baseline, Week 52
Secondary Percentage of Participants Who Achieved Weight Loss of =5% Week 52
Secondary Percentage of Participants Who Achieved Weight Loss of =10% Week 52
Secondary Percentage of Participants Who Achieved Weight Loss of =15% Week 52
Secondary Change from Baseline in Systolic Blood Pressure (SBP) Baseline, Week 52
Secondary Change from Baseline in Diastolic Blood Pressure (DBP) Baseline, Week 52
Secondary Percentage Change from Baseline in Total Cholesterol Baseline, Week 52
Secondary Percentage Change from Baseline in High Density Lipoprotein (HDL)-Cholesterol Baseline, Week 52
Secondary Percentage Change from Baseline in Low Density Lipoprotein (LDL)-Cholesterol Baseline, Week 52
Secondary Percentage Change from Baseline in Very Low Density Lipoprotein (VLDL)-Cholesterol Baseline, Week 52
Secondary Percentage Change from Baseline in Non-HDL-Cholesterol Baseline, Week 52
Secondary Percentage Change from Baseline in Triglycerides Baseline, Week 52
Secondary Change from Baseline in Short Form 36 Version 2 (SF-36-v2) Acute Form Domain Summary Scores Baseline, Week 52
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