NICE backs Merck & Co's Prevymis for CMV

30 May 2019
merck_co_large

The National Institute for Health and Care Excellence (NICE) has published its Final Appraisal Document for the use of Merck & Co’s (NYSE: MRK) Prevymis (letermovir/ID1153) in preventing cytomegalovirus (CMV) reactivation and disease in patients receiving an allogeneic stem cell transplant.

Prevymis, a member of a new class of drugs called non-nucleoside CMV inhibitors, is recommended by the cost watchdog for England, Wales and Northern Ireland, in adults who are seropositive for CMV.

The recommendation for the drug’s provision on the National Health Service (NHS) comes after the US pharma giant came to a commercial agreement with the NICE.

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