Semaglutide: First Global Approval.

Abstract:

:Novo Nordisk has developed a subcutaneous formulation of semaglutide (Ozempic®), a modified human glucagon-like peptide-1 (GLP-1) analogue, for the treatment of type 2 diabetes mellitus. It has been developed using Novo Nordisk's proprietary protein-acylation technology, and is administered using an injection device. Semaglutide lowers blood glucose by stimulating the release of insulin and also lowers body weight. Once-weekly subcutaneous semaglutide has recently been approved in the US, Puerto Rico and Canada, and has received a positive opinion in the EU for the treatment of patients with type 2 diabetes. It will be launched as the Ozempic® Pen, a pre-filled device. Semaglutide is also under regulatory review in Japan and Switzerland for the treatment of type 2 diabetes. Clinical development for obesity, non-alcoholic steatohepatitis and non-alcoholic fatty liver disease is underway worldwide. This article summarizes the milestones in the development of semaglutide leading to this first approval for type 2 diabetes.

journal_name

Drugs

journal_title

Drugs

authors

Dhillon S

doi

10.1007/s40265-018-0871-0

subject

Has Abstract

pub_date

2018-02-01 00:00:00

pages

275-284

issue

2

eissn

0012-6667

issn

1179-1950

pii

10.1007/s40265-018-0871-0

journal_volume

78

pub_type

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