Exenatide for the treatment of type 2 diabetes mellitus

Ruddock B
Record ID 32005001200
English, French
Authors' objectives: The aim of this report is to summarize the available information on the use of exenatide as an add-on therapy for patients with type 2 diabetes mellitus who are taking oral antidiabetic drugs.
Authors' recommendations: Evidence indicates that exenatide reduces glycosylated hemoglobin and plasma glucose levels when compared with placebo. Limitations of the therapy include the need for twice daily injections and potentially dose-limiting nausea and vomiting. Long-term studies are required to determine the effects of exenatide on disease related morbidity and mortality.
Authors' methods: Overview
Details
Project Status: Completed
Year Published: 2005
URL for published report: n/a
English language abstract: An English language summary is available
Publication Type: Not Assigned
Country: Canada
MeSH Terms
  • Costs and Cost Analysis
  • Hypoglycemic Agents
  • Diabetes Mellitus, Type 2
  • Exenatide
Contact
Organisation Name: Canadian Coordinating Office for Health Technology Assessment
Contact Address: 600-865 Carling Avenue, Ottawa, ON K1S 5S8 Canada. Tel: +1 613 226 2553, Fax: +1 613 226 5392;
Contact Name: requests@cadth.ca
Contact Email: requests@cadth.ca
Copyright: Canadian Coordinating Office for Health Technology Assessment (CCOHTA)
This is a bibliographic record of a published health technology assessment from a member of INAHTA or other HTA producer. No evaluation of the quality of this assessment has been made for the HTA database.