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It looks like it is now just a matter of time before Exenatide LAR, (once a week Byetta) gets the final approval from the FDS……
Amylin Eli Lilly and Alkermes, announced that the New Drug Application (NDA) for exenatide once weekly has been accepted for review by the U.S. Food and Drug Administration (FDA).
Exenatide once weekly is an investigational sustained release medication for Type 2 diabetes that is injected subcutaneously and administered only once a week. Exenatide is the active ingredient in BYETTA® (exenatide) injection, which is currently available in the U.S. and in many countries worldwide for people with Type 2 diabetes who are unable to achieve good glycemic control with common oral therapies.
“Acceptance of the NDA submission for exenatide once weekly is an important milestone both in the exenatide development program and in the treatment of Type 2 diabetes,” said Orville G. Kolterman, M.D., senior vice president of research and development at Amylin Pharmaceuticals. “If approved, this therapy could fill an important unmet need for treating patients with Type 2 diabetes with just one dose per week.”
BYETTA is the first and only FDA-approved incretin mimetic for the treatment of Type 2 diabetes. BYETTA exhibits many of the same effects as the human incretin hormone glucagon like peptide-1 (GLP-1). GLP-1 improves blood sugar after food intake through multiple effects that work in concert on the stomach, liver, pancreas and brain. BYETTA is approved by the FDA for use by people with Type 2 diabetes who are unsuccessful at controlling their blood sugar levels. BYETTA is an add-on therapy for people currently using metformin, a sulfonylurea, or a thiazolidinedione. BYETTA provides sustained A1c control and low incidence of hypoglycemia when used with metformin or a thiazolidinedione, with potential weight loss. BYETTA is not a weight loss product. BYETTA was approved in April 2005 and has been used by more than one million patients since its introduction.