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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03730662
Other study ID # 17072
Secondary ID I8F-MC-GPGM2018-
Status Completed
Phase Phase 3
First received
Last updated
Start date November 20, 2018
Est. completion date April 22, 2021

Study information

Verified date January 2022
Source Eli Lilly and Company
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the trial is to assess the efficacy and safety of tirzepatide taken once a week to insulin glargine taken once daily in participants with type 2 diabetes and increased cardiovascular risk. The study will last about 108 weeks and may include up to 30 visits.


Recruitment information / eligibility

Status Completed
Enrollment 2002
Est. completion date April 22, 2021
Est. primary completion date January 22, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: Participants must: - Have been diagnosed with type 2 diabetes mellitus (T2DM) - Have HbA1c between =7.5% and =10.5% - Be on stable treatment with unchanged dose of at least 1 and no more than 3 types of oral antihyperglycemic drugs, which may only include metformin, SGLT-2 inhibitors, and/or sulfonylureas for at least 3 months before screening - Have increased risk for cardiovascular (CV) events - Be of stable weight (± 5%) - Have a BMI =25 kilograms per meter squared (kg/m2) at screening Exclusion Criteria Participants must not: - Have type 1 diabetes mellitus - Have had chronic or acute pancreatitis any time prior to study entry - Have proliferative diabetic retinopathy or diabetic maculopathy or nonproliferative diabetic retinopathy requiring immediate or urgent treatment - Have disorders associated with slowed emptying of the stomach, or have had any stomach surgeries for the purpose of weight loss - Have acute or chronic hepatitis, signs and symptoms of any other liver disease, or blood alanine transaminase (ALT) enzyme level >3.0 times the upper limit of normal (ULN) for the reference range, as determined by the central laboratory. Participants with nonalcoholic fatty liver disease (NAFLD) are eligible for participation in this trial only if there ALT level is =3.0 the ULN for the reference range - Have had a heart attack, stroke, or hospitalization for congestive heart failure in the past 2 months - Have a personal or family history of medullary thyroid carcinoma or personal history of multiple endocrine neoplasia syndrome type 2 - Have been taking any other diabetes medicines other than metformin, SGLT-2 inhibitors, and/or sulfonylureas during the last 3 months - Have been taking weight loss drugs, including over-the-counter medications during the last 3 months

Study Design


Intervention

Drug:
Tirzepatide
Administered SC.
Insulin Glargine
Administered SC

Locations

Country Name City State
Argentina AXISMED SRL - Bioclinica Research Network Buenos Aires
Argentina CEDIC-Centro de Investigaciones Clinicas Caba Buenos Aires
Argentina CEMEDIC Caba Buenos Aires
Argentina Centro de Investigaciones Metabólicas (CINME) Caba Buenos Aires
Argentina Investigaciones Medicas IMOBA S.R.L. Caba Buenos Aires
Argentina Mautalen Salud e Investigación - Servicio de Endocrinología Caba Buenos Aires
Argentina Centro de Investigacion y Prevencion Cardiovascular (CIPREC) Ciudad Autonoma de Buenos Aires
Argentina Cemediab - Centro Médico Diabetológico Dr. Alejandro Chertkoff Ciudad Autonoma de Buenos Aire
Argentina Centro Medico Dr Laura Maffei Investigacion Clinica Aplicada Ciudad Autonoma de Buenos Aire Buenos Aires
Argentina Centro Médico Viamonte Ciudad Autonoma de Buenos Aire
Argentina Instituto Centenario Ciudad Autonoma de Buenos Aire
Argentina Cent Priva Especiali Médicas Ambulatorias Inve Clin CEMAIC Cordoba
Argentina Centro Diabetologico Dr Waitman Cordoba
Argentina Centro Medico Privado San Vicente Diabetes Cordoba
Argentina CIPADI Godoy Cruz Mendoza
Australia Paratus Clinical Blacktown Clinic Blacktown New South Wales
Australia Eastern Clinical Research Unit Box Hill Victoria
Australia CORE Research Group Pty Ltd Brisbane Queensland
Australia Campbelltown Medical & Dental Centre Campbelltown New South Wales
Australia Forest Hill Medical and Dental Centre Forest Hill Victoria
Australia Fremantle Hospital Fremantle Western Australia
Australia Barwon Health - The Geelong Hospital Geelong Victoria
Australia Paratus Clinical Kanwal Clinic Kanwal New South Wales
Australia The AIM Centre Merewether New South Wales
Australia Morayfield Medical and Dental Centre Morayfield Queensland
Australia GP Plus Marion Oaklands Park South Australia
Australia Royal Melbourne Hospital Parkville Victoria
Australia AusTrials Pty Ltd Sherwood Queensland
Australia Royal North Shore Hospital St. Leonards New South Wales
Australia Victoria Point Medical and Dental Centre Victoria Point Queensland
Brazil Centro de Pesquisa Clinica do Brasil Brasilia Distrito Federal
Brazil Centro de Diabetes Curitiba Curitiba Parana
Brazil Centro de Pesq. em Diabetes e Doencas Endocrino Metabol. Fortaleza
Brazil Instituto de Ensino e Pesquisa Clinica do Ceara Fortaleza Ceara
Brazil CCBR Brasil Centro de Analises e Pesquisas Clínicas LTDA Rio de Janeiro RJ
Brazil Cpclin Centro de Pesquisas Clinicas São Paulo SP
Brazil CPQuali Pesquisa Clínica Ltda. São Paulo SP
Brazil Dr. Consulta Clínica Médica LTDA São Paulo
Brazil Cedoes Centro Diagnostico Pequisa Osteoporose E Santo Ltd Vitoria ES
Canada LMC Endocrinology Centres Ltd. Barrie Ontario
Canada Aggarwal and Associates Ltd Brampton Ontario
Canada LMC Endocrinology Centers Brampton Brampton Ontario
Canada C-Health Diabetes and Endocrinology Clinic Calgary Calgary Alberta
Canada LMC Manna Research Calgary Alberta
Canada LMC Endocrinology Centres Ltd. Concord Ontario
Canada Q & T Research Outaouais Gatineau Quebec
Canada Centre De Recherche Clinique De Laval Laval Quebec
Canada Manna Research (Quebec) Levis Quebec
Canada Milestone Research Inc. London Ontario
Canada LMC Endocrinology Centres Ltd. Nepean Ontario
Canada Bluewater Clinical Research Group Inc Sarnia Ontario
Canada Synergy Medical Research Sherwood Park Alberta
Canada Canadian Centre for Research on Diabetes Smiths Falls Ontario
Canada Manna Research, Inc. Stoney Creek Ontario
Canada Medicor Research Inc Sudbury Ontario
Canada LMC Endocrinology Centres Ltd. Toronto Ontario
Canada LMC Endocrinology Centres Ltd. Ville St-Laurent Quebec
Canada Sameh Fikry Medicine Professional Corporation Waterloo Ontario
Greece University General Hospital of Larissa Larissa
Greece Iatriko Palaiou Falirou, Medical Center Palaio Faliro Athens
Greece Thermi Clinic Thermi Thessaloniki
Greece AHEPA Hospital Thessaloniki
Greece Euromedica - General Clinic of Thessaloniki Thessaloniki
Israel Ha'Emek Medical Center Afula
Israel Soroka Medical Center Beer Sheva
Israel Rambam Medical Center Haifa
Israel Wolfson Medical Center Holon
Israel Hadassah Medical Center Jerusalem
Israel Rabin Medical Center Petach Tikva
Israel Sheba Medical Center Ramat Gan
Israel Sakhnin Community Clinic, Clalit Health Services Sakhnin
Israel Tel Aviv Sourasky Medical Center Tel Aviv Jaffa
Mexico Investigacion en Salud y Metabolismo S.C Chihuahua
Mexico Diseno y Planeacion en Investigacion Medica S.C. Guadalajara Jalisco
Mexico Instituto Jalisciense de Investigacion en Diabetes y Obesida Guadalajara Jalisco
Mexico St. Lucas Clinical Research Center Merida Mexico State
Mexico Unidad Medica para la Salud Integral (UMSI) Monterrey Nuevo León
Mexico Centro de Estudios de Investigacion Metabolicos y Cardiovasc Tampico Tamaulipas
Poland Poradnia Diabetologiczna SN ZOZ Lege Artis Bialystok
Poland NZOZ Diab-Endo-Met Krakow
Poland Centrum Terapii Wspolczesnej J.M. Jasnorzewska S.K.A. Lodz
Poland Gabinety Terpa Lublin
Poland NZOZ CenterMed Lublin Lublin
Poland NZOZ Przychodnia Specjalistyczna MEDICA Lublin
Poland Nzoz Neuro - Kard Poznan
Poland Praktyka Lekarska Poznan
Poland NZOZ Przychodnia Specjalistyczna Henryk RudzkiAndrzej Wittek Ruda Slaska
Poland Centralny Szpital Kliniczny MSWiA Klinika Dermatologiczna Warszawa Mazowieckie
Poland Woj. Zesp. Spec. Opieki Zdrowotnej Wroclaw
Puerto Rico Emanuelli Research & Development Center, LLC Arecibo
Puerto Rico Manati Center for Clinical Research Inc Manati
Puerto Rico Ponce School of Medicine CAIMED Center Ponce
Puerto Rico Research and Cardiovascular Corp. Ponce
Puerto Rico University Of Puerto Rico Rio Pedras
Puerto Rico Consultorio Medico San Juan
Puerto Rico GCM Medical Group PSC San Juan
Romania CMI DNBM Dr. Pop Lavinia Baia Mare Maramures
Romania Centrul Medical de Diagnostic si Tratament Ambulatoriu Neomed SRL Brasov
Romania Cabinetul Medical Nicodiab SRL Bucharest
Romania SC Nutrilife SRL Bucuresti
Romania Milena Sante SRL Galati
Romania SC Gama Diamed SRL Mangalia Constanta
Romania Spitalul Judetean de Urgenta Satu Mare Satu-Mare Jud Satu-Mare
Romania Cosamext SRL Targu Mures Mures
Romania Centrul Medical Dr. Negrisanu Timisoara Timis
Russian Federation Arkhangelsk the first city clinical hospital Arkhangelsk
Russian Federation FSBI Endocrinological Research Center of the MOH of the ROF Moscow
Russian Federation Novosibirsk Regional Clinical Hospital Novosibirsk
Russian Federation Ryazan Regional Clinincal Cardiology Dispensary Ryazan
Russian Federation City Hospital of Saint Martyr Elizabeth Saint Petersburg
Russian Federation Medical Military Academy Saint Petersburg
Russian Federation SPb GUZ "Diagnostic Center #85" Saint Petersburg
Russian Federation City Consultative and Diagnostic Center Saint-Petersburg
Russian Federation Regional Clinical Hospital Saratov
Russian Federation Research & Practice Ltd Yaroslavl
Slovakia Human care s.r.o. Kosice Slovak Republic
Slovakia MediVet s.r.o. Malacky Slovak Republic
Slovakia DIA-MED CENTRUM s.r.o. Puchov
Slovakia Tatratrial s.r.o. Roznava
Slovakia MEDI-DIA s.r.o. Sabinov
Slovakia Areteus s.r.o. Trebisov Slovak Republic
Spain Hospital de la Ribera Alcira Valencia
Spain Instituto de Ciencias medicas Alicante
Spain Centro Periférico de Especialidades Bola Azul Almeria
Spain Hospital Quironsalud Barcelona- END Barcelona
Spain Hospital Clinico Universitario San Cecilio Granada
Spain Complexo Hospitalario Universitario A Coruña, CHUAC La Coruña
Spain Centro Especialidades San Jose Obrero (Barbarela) Malaga
Spain Clinica Juaneda Palma de Mallorca
Spain Hospital Universitario Quiron Madrid Pozuelo de Alarcon Madrid
Spain Hospital Universitario Marques De Valdecilla Santander Cantabria
Spain Hospital Universitario Virgen Macarena Sevilla
Spain Clinica Nuevas Tecnologias en Diabetes y Endocrinologia Seville
Taiwan Chang Gung Memorial Hospital - Kaohsiung Kaohsiung City
Taiwan Cardinal Tien Hospital Sindian City Taipei County
Taiwan China Medical University Hospital Taichung
Taiwan Chung Shan Medical University Hospital Taichung City
Taiwan Kuang Tien General Hospital Taichung County
Taiwan National Cheng Kung University Hospital Tainan
Taiwan Chi-Mei Medical Center Tainan City
Taiwan Taipei Veterans General Hospital Taipei
Taiwan National Taiwan University Hospital Taipei City
United States Advanced Research Center Anaheim California
United States Primary Care Specialists, LLC Atlanta Georgia
United States Heritage Valley Medical Group, Inc. Beaver Pennsylvania
United States Burke Internal Medicine & Research Burke Virginia
United States Capital Area Research Camp Hill Pennsylvania
United States Clinical Research Professionals Chesterfield Missouri
United States Northwestern Feinberg School of Medicine Chicago Illinois
United States Rapid Medical Research Inc Cleveland Ohio
United States Aventiv Research Columbus Ohio
United States Ohio State Univ College Of Medicine Columbus Ohio
United States ALL Medical Research, LLC Cooper City Florida
United States The Corvallis Clinic P.C. Corvallis Oregon
United States Valley Clinical Trials, Inc. Covina California
United States Advanced Pharma Research Cutler Bay Florida
United States Dallas Diabetes Endocrine Center Dallas Texas
United States NECCR PrimaCare Research, LLC Fall River Massachusetts
United States Lillestol Research LLC Fargo North Dakota
United States Alpine Research Organization Farmington Utah
United States Private: Dr. Larry Stonesifer Federal Way Washington
United States AA Medical Research Center Flint Michigan
United States Marin Endocrine Associates Greenbrae California
United States PharmQuest Greensboro North Carolina
United States Mountain View Clinical Research, Inc. Greer South Carolina
United States PCP for Life Houston Texas
United States National Research Institute Huntington Park California
United States Rocky Mountain Diabetes and Osteoporosis Center Idaho Falls Idaho
United States University of Iowa Hospital & Clinic Iowa City Iowa
United States Glacier View Research Institute Kalispell Montana
United States Holston Medical Group Clinical Research Kingsport Tennessee
United States New Phase Research & Development Knoxville Tennessee
United States Scripps Whittier Diabetes Institute La Jolla California
United States First Valley Medical Group Lancaster California
United States Detweiler Family Medicine Lansdale Pennsylvania
United States Palm Research Center Las Vegas Nevada
United States Palm Research Center Las Vegas Nevada
United States National Research Institute Los Angeles California
United States Robley Rex VAMC Louisville Kentucky
United States South Florida Wellness & Clinical Research Institute Margate Florida
United States The Research Center of the Upstate Mauldin South Carolina
United States Solaris Clinical Research Meridian Idaho
United States New Horizon Research Center Miami Florida
United States Suncoast Research Group, LLC Miami Florida
United States Montana Medical Research, Inc Missoula Montana
United States Catalina Research Institute, LLC Montclair California
United States Monterey Endocrine & Diabetes Institute, Inc. Monterey California
United States Saltzer Medical Group. P.A. Nampa Idaho
United States Southern New Hampshire Diabetes and Endocrinology Nashua New Hampshire
United States Capital Area Research Newport Pennsylvania
United States Intend Research Norman Oklahoma
United States Valley Clinical Trials, Inc. Northridge California
United States Capital Clinical Research Center Olympia Washington
United States Clinical Neuroscience Solutions Inc Orlando Florida
United States Desert Medical Group Inc Palm Springs California
United States Havana Research Institute Pasadena California
United States Parkside Family Medical Philadelphia Pennsylvania
United States Preferred Primary Care Physicians- Bower Hill Pittsburgh Pennsylvania
United States Western University of Health Sciences Pomona California
United States Progressive Medical Research Port Orange Florida
United States Oregon Health and Science University Portland Oregon
United States BFHC Research San Antonio Texas
United States LCGK Research San Carlos California
United States Consano Clinical Research Shavano Park Texas
United States NorthShore University HealthSystem Skokie Illinois
United States Olive View Medical Center Sylmar California
United States Martin Diagnostic Clinic Tomball Texas
United States Cotton O'Neil Diabetes and Endocrinology Center Topeka Kansas
United States Troy Internal Medicine, PC Troy Michigan
United States University Clinical Investigators, Inc. Tustin California
United States Touro University Vallejo California
United States Coastal Metabolic Research Centre Ventura California
United States Walla Walla Clinic Walla Walla Washington
United States Diablo Clinical Research Walnut Creek California
United States Chase Medical Research, LLC Waterbury Connecticut
United States Iowa Diabetes Research West Des Moines Iowa

Sponsors (1)

Lead Sponsor Collaborator
Eli Lilly and Company

Countries where clinical trial is conducted

United States,  Argentina,  Australia,  Brazil,  Canada,  Greece,  Israel,  Mexico,  Poland,  Puerto Rico,  Romania,  Russian Federation,  Slovakia,  Spain,  Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change From Baseline in Hemoglobin A1c (HbA1c) (10 mg and 15 mg) HbA1c is the glycosylated fraction of hemoglobin A. HbA1c is measured primarily to identify average plasma glucose concentration over prolonged periods of time. Least Squares (LS) mean was determined by mixed-model repeated measures (MMRM) model for post-baseline measures: Variable = Baseline + Pooled Country + Baseline sodium-glucose co-transporter-2 inhibitor (SGLT-2i) use Flag (Yes, No) + Treatment + Time + Treatment*Time (Type III sum of squares). Baseline, Week 52
Secondary Change From Baseline in HbA1c (5 mg) HbA1c is the glycosylated fraction of hemoglobin A. HbA1c is measured primarily to identify average plasma glucose concentration over prolonged periods of time. LS mean was determined by MMRM model for post-baseline measures: Variable = Baseline + Pooled Country + Baseline SGLT-2i use Flag (Yes, No) + Treatment + Time + Treatment*Time (Type III sum of squares). Baseline, Week 52
Secondary Change From Baseline in Body Weight LS mean was determined by MMRM model for post-baseline measures: Variable = Baseline + Pooled Country + Baseline HbA1c Group (<=8.5%, >8.5%) + Baseline SGLT-2i use Flag (Yes, No) + Treatment + Time + Treatment*Time (Type III sum of squares). Baseline, Week 52
Secondary Percentage of Participants With HbA1c of <7.0% HbA1c is the glycosylated fraction of hemoglobin A. HbA1c is measured primarily to identify average plasma glucose concentration over prolonged periods of time. Imputed data includes observed value and imputed value if endpoint measure is missing. Week 52
Secondary Change From Baseline in Fasting Serum Glucose LS mean was determined by MMRM model for post-baseline measures: Variable = Baseline + Pooled Country + Baseline HbA1c Group (<=8.5%, >8.5%) + Baseline SGLT-2i use Flag (Yes, No) + Treatment + Time + Treatment*Time (Type III sum of squares). Baseline, Week 52
Secondary Mean Change From Baseline in Daily Average 7-Point Self-Monitored Blood Glucose (SMBG) Values The self-monitored plasma glucose (SMBG) data were collected at the following 7 time points: Morning Premeal - Fasting, Morning 2-hour Postmeal, Midday Premeal, Midday 2-hour Postmeal, Evening Premeal, Evening 2-hour Postmeal and Bedtime. LS mean was determined by mixed-model repeated measures (MMRM) model with variables Baseline + Pooled Country + Baseline HbA1c Group (<=8.5%, >8.5%) + Baseline SGLT-2i use Flag (Yes, No) + Treatment + Time + Treatment*Time (Type III sum of squares). Baseline, Week 52
Secondary Pharmacokinetics (PK): Steady State Area Under the Concentration Time Curve From Zero to Tau (AUC 0-Tau) of Tirzepatide Pharmacokinetics (PK): Steady State Area Under the Concentration Time Curve From Zero to Tau (AUC 0-Tau) of Tirzepatide 1 to 24 hours, 24 to 96 hours, or 120 to 168 hours post dose of Week 7, 15, 23, 35
Secondary Rate of Hypoglycemia With Blood Glucose <54 Milligram/Deciliter (mg/dL) [<3.0 (Millimole/Liter (mmol/L))] or Severe Hypoglycemia The hypoglycemia events were defined by participant reported events with blood glucose <54mg/dL (<3.0 mmol/L) or severe hypoglycemia. Severe hypoglycemia is defined as an episode with severe cognitive impairment requiring the assistance of another person to actively administer carbohydrate, glucagon, or other resuscitative actions. These episodes may be associated with sufficient neuroglycopenia to induce seizure or coma. Post-baseline comparisons between treatment and control group was evaluated using negative binomial model with variables : Number of episodes = Baseline HbA1c Group (<=8.5%, >8.5%) + Pooled Country + Baseline SGLT-2i use Flag (Yes, No) + Treatment, with log (exposure in days/365.25) as an offset variable Baseline through Week 52
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