Janssen, a subsidiary of US health care giant Johnson & Johnson, said today that it welcomes the publication of the Final Appraisal Determination (FAD) from UK drugs watchdog the National Institute for Health and Care Excellence (NICE), for Invokana (canagliflozin), a new treatment option indicated for reducing blood glucose levels in people for whom diet and lifestyle measures or treatment with other blood glucose-lowering medicines, do not provide adequate control.
Canagliflozin also has the additional benefits of modest weight loss (2%-3%) and blood pressure reduction (although is not licensed for use in weight loss or blood pressure reduction), Janssen noted.
This announcement comes just two months after the UK launch of canagliflozin. The NICE FAD recommends canagliflozin to be used as a treatment for adults with type 2 diabetes, as either dual therapy(in combination with metformin, only if a sulfonylurea is contraindicated or not tolerated, orwhere the person is at significant risk of hypoglycemia or its consequences) or triple therapy(in combination with metformin and a sulfonylurea, or metformin and thiazolidinedione), or in combination with insulin(with or without other antidiabetic therapies).
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