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Search / Trial NCT00676338

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

Amylin Lilly Exenatide Once Weekly Byetta Januvia Sitagliptin Thiazolidinedione

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  • Have previously completed or discontinued study drug in this study, withdrawn from this study or any other study investigating exenatide once weekly.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.

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

0 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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