Safety and Efficacy of Exenatide Once Weekly Injection Versus Metformin, Dipeptidyl Peptidase-4 Inhibitor, or Thiazolidinedione as Monotherapy in Drug-Naive Patients With Type 2 Diabetes (DURATION-4)
Launched by ASTRAZENECA · May 9, 2008
Trial Information
Current as of May 04, 2025
Completed
Keywords
ClinConnect Summary
No description provided
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • have type 2 diabetes and are treated with diet and exercise alone.
- • at least 18 years of age.
- • HbA1c between 7.1% and 11.0%, inclusive.
- • Body mass index (BMI) of 23 kg/m2 to 45 kg/m2, inclusive.
- • Have a history of stable body weight (not varying by \>5% for at least 3 months prior to screening).
- Exclusion Criteria:
- • Have history of cardiac disease or presence of active cardiac disease within the year prior to inclusion in the study including myocardial infarction, clinically significant arrhythmia, unstable angina, moderate to severe congestive heart failure, coronary artery bypass surgery, or angioplasty
- • Have a history of renal transplantation or are currently receiving renal dialysis
- • Have active or untreated malignancy, or have been in remission from clinically significant malignancy (other than basal cell or squamous cell skin cancer, in situ carcinomas of the cervix, or in situ prostate cancer) for less than 5 years.
- • Have history of severe GI disorder (e.g., gastroparesis)
- • Have a history of acute or chronic pancreatitis.
- • Have active proliferative retinopathy.
- • Have been treated with drugs that promote weight loss (e.g., Xenical®\[orlistat\], Meridia® \[sibutramine\], Acomplia® \[rimonabant\], Acutrim® \[phenylpropanolamine\], or similar over-the-counter medications) within 3 months of screening.
- • Have been treated with any antidiabetic agent for more than 7 days within 3 months prior to screening.
- • Have had an organ transplant.
- • Have previously completed or discontinued study drug in this study, withdrawn from this study or any other study investigating exenatide once weekly.
- • Have received treatment within the last 30 days with a drug that has not received regulatory approval for any indication at the time of study entry.
- • Are currently enrolled in any other clinical study.
About Astrazeneca
AstraZeneca is a global biopharmaceutical company dedicated to the discovery, development, and commercialization of innovative medicines across various therapeutic areas, including oncology, cardiovascular, respiratory, and autoimmune diseases. With a strong commitment to scientific research and patient-centric solutions, AstraZeneca leverages cutting-edge technology and a robust pipeline to address unmet medical needs. The company collaborates with healthcare professionals, academic institutions, and other organizations to advance clinical trials and deliver transformative therapies, aiming to improve health outcomes and enhance the quality of life for patients worldwide.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Los Angeles, California, United States
Jacksonville, Florida, United States
Atlanta, Georgia, United States
Des Moines, Iowa, United States
Grand Rapids, Michigan, United States
Minneapolis, Minnesota, United States
Billings, Montana, United States
Wilmington, North Carolina, United States
Danville, Pennsylvania, United States
Philadelphia, Pennsylvania, United States
Austin, Texas, United States
El Paso, Texas, United States
Budapest, , Hungary
Buenos Aires, , Argentina
Mainz, , Germany
Johannesburg, , South Africa
Edinburgh, , United Kingdom
Toms River, New Jersey, United States
Mar Del Plata, , Argentina
Leuven, , Belgium
Curitiba, , Brazil
Porto Alegre, , Brazil
Mississauga, , Canada
Saint John, , Canada
Holon, , Israel
Tel Hashomer, , Israel
Seoul, , Korea, Republic Of
Chihuahua, , Mexico
Guadalajara, , Mexico
Lublin, , Poland
Szczecin, , Poland
Moscow, , Russian Federation
Penticton, British Columbia, Canada
Ottawa, Ontario, Canada
Sevilla, Andalucia, Spain
Barcelona, Cataluna, Spain
Madrid, Comunidad De Madrid, Spain
Pune, , India
Milano, , Italy
Nantes, , France
Monterrey, , Mexico
Ankara, , Turkey
Istanbul, , Turkey
Saint Petersburg, , Russian Federation
Sheffield, , United Kingdom
Bangalore, , India
Gyula, , Hungary
Pecs, , Hungary
Firenze, , Italy
Galati, , Romania
Bratislava, , Slovakia
Dresden, , Germany
Oradea, , Romania
Wroclaw, , Poland
Guildford, , United Kingdom
Arkhangelsk, , Russian Federation
Rostov On Don, , Russian Federation
Stavropol, , Russian Federation
New Dehli, , India
Hull, , United Kingdom
Bath, , United Kingdom
Fortaleza, , Brazil
Muenster, , Germany
Mumbai, , India
Meridian, Idaho, United States
Marchovelette, , Belgium
Tessenderlo, , Belgium
Campinas, , Brazil
Coquitlam, British Columbia, Canada
Swansea, , United Kingdom
Birmingham, West Midlands, United Kingdom
Vieux Conde, , France
Recife, , Brazil
Targu Mures, , Romania
Ahmedabad, , India
Daegu, , Korea, Republic Of
Jeonju, , Korea, Republic Of
Busan, , Korea, Republic Of
Frome, , United Kingdom
Manati, , Puerto Rico
Buena Park, California, United States
Rodgau, , Germany
Cochin, , India
Siena, Si, Italy
Alicante, Comunidad Valenciana, Spain
Murs Erigne, , France
Valencia, California, United States
Wilke Barre, Pennsylvania, United States
New Branufels, Texas, United States
Brasilia, , Brazil
Joinville, , Brazil
Sao Paolo, , Brazil
Gatineu, Quebec, Canada
Petitcodiac, , Canada
Pointe Claire, , Canada
Regina, , Canada
Chateaugiron, , France
Hodmezovasarhely, , Hungary
Channai, , India
Sungnam, , Korea, Republic Of
Toa Baja, , Puerto Rico
Trebisov, , Slovakia
Kempton Park, , South Africa
Midrand, , South Africa
Soweto, , South Africa
Sisli Istanbul, , Turkey
Patients applied
Trial Officials
Chief Medical Officer, MD
Study Director
Eli Lilly and Company
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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