Home > PJ (current issue) > News / News Centre | Search

PJ Online homeThe Pharmaceutical Journal
Vol 278 No 7443 p298
17 March 2007

This article
Reprint   Photocopy

  Acrobat Reader


News summary


First in a new class of medicines to treat type 2 diabetes launched

Exenatide (Byetta), the first in a new class of medicines to treat type 2 diabetes, was launched at the Diabetes UK annual conference in Glasgow this week.

Exenatide is an incretin mimetic developed by Lilly and Amylin Pharmaceuticals. It works by improving beta cell function by mimicking the effects of a naturally occurring incretin hormone protein called glucagon-like peptide-1. Exenatide also suppresses inappropriate secretion of glucagon, which is common in people with type 2 diabetes; this decreases beta cell workload and increases beta cell response. It also slows emptying of food from the stomach.

Exenatide is indicated for the treatment of type 2 diabetes mellitus in combination with metformin or sulphonylureas, or both, in patients who have not achieved adequate glycaemic control on maximally tolerated doses of these oral therapies. It is given twice daily by subcutaneous injection up to 60 minutes before a main meal. The dose does not need to be altered to match meal size or planned activities. In clinical trials exenatide reduced HbA1c and body weight in three placebo-controlled studies when added to metformin, a sulphonylurea, or both (PJ, 12 June 2004, p733).

Shailen Rao, an independent consultant pharmacist with experience of diabetes care, told The Journal: “Exenatide provides a welcome addition to the current treatment options for patients with type 2 diabetes. Its effect on body weight is of particular interest and importance in this group of patients.”

Exenatide is expected to be available in the UK from May 2007.


Notice-board p305

Back to Top


©The Pharmaceutical Journal