UK drug watchdog the National Institute for Health and Clinical Excellence (NICE) has today (March 9) issued final draft guidance recommending Victrelis (boceprevir) in combination with peginterferon alfa and ribavirin, as an option for the treatment of genotype 1 chronic hepatitis C in adults with compensated liver disease.
US drug giant Merck & Co’s (NYSE: MRK) Victrelis, which has received regulatory approval in Europe and the USA, is the first major advancement for the treatment of chronic hepatitis C approved in a decade.
Figures from 2009 suggest that around 146,000 people in England and Wales were chronically infected with the hepatitis%-50% of people with hepatitis - and the most resistant to treatment. Poor diagnosis rates, low treatment compliance rates and a high annual incidence of new infection mean that chronic hepatitis C presents a major public health challenge, despite the availability of treatments that provide the opportunity to address this challenge, the NICE noted.
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