Adding to US approval early last year for their combination diabetes product, German family-owned drug major Boehringer Ingelheim and USA-based Eli Lilly (NYSE: LLY) have received clearance to market it in Europe.
The companies announced that Glyxambi (empagliflozin/linagliptin) has been granted marketing authorisation by the European Commission for use in adults with type 2 diabetes (T2D). Glyxambi is a single pill combining Jardiance (empagliflozin), a sodium glucose co-transporter-2 (SGLT2) inhibitor, and Trajenta (linagliptin), a dipeptidyl peptidase-4 (DPP-4) inhibitor.
Glyxambi is approved for use in adults with T2D to improve blood sugar control when metformin and/or sulphonylurea and one of the monocomponents of Glyxambi do not provide adequate blood sugar control, or when a patient is already being treated with the free combination of Jardiance and Trajenta.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze