Combo approved in EU across major HCV genotypes

28 July 2017
2019_biotech_test_vial_discovery_big

The European Commission has granted Maviret (glecaprevir/pibrentasvir) marketing authorization for chronic hepatitis C virus (HCV) in all major genotypes.

This treatment, discovered during the ongoing collaboration between US drugmaker AbbVie (NYSE: ABBV) and biotech firm Enanta Pharmaceuticals (Nasdaq:ENTA), is a new eight-week, pan-genotypic treatment for adult HCV without cirrhosis and who are new to treatment.

Alice Butler, medical director of AbbVie UK, said: “The treatment combines two distinct anti-viral agents and has high efficacy against most HCV genotypes, including those commonly associated with resistance to treatment.”

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 account

Become a subscriber

 

£820

Or £77 per month

Subscribe Now
  • Unfettered access to industry-leading news, commentary and analysis in pharma and biotech.
  • Updates from clinical trials, conferences, M&A, licensing, financing, regulation, patents & legal, executive appointments, commercial strategy and financial results.
  • Daily roundup of key events in pharma and biotech.
  • Monthly in-depth briefings on Boardroom appointments and M&A news.
  • Choose from a cost-effective annual package or a flexible monthly subscription
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

Companies featured in this story

More ones to watch >


Today's issue

Company Spotlight





More Features in Biotechnology