EC approves Bydureon BCise device for T2 diabetes
30 August 2018 07:00 BST European Commission approves new easy-to-use, once-weekly Bydureon BCise device for patients with type-2 diabetes AstraZeneca today announced that the European Commission (EC) has approved Bydureon BCise (exenatide 2mg prolonged-release suspension for injection in pre-filled pen) as a new formulation within the marketing authorisation for Bydureon (exenatide extended release) for the treatment of patients with type-2 diabetes. The new formulation of once-weekly Bydureon is an improved single-dose, pre-filled pen device that requires no titration and is