Still strong a decade on, Gilenya gains approval in China

19 July 2019
china_beijing_big

Nearly 10 years after garnering approval in the USA, multiple sclerosis (MS) therapy Gilenya (fingolimod) has finally been given the green light for marketing in China, where the condition is classed as a rare disease.

The Chinese National Medical Products Administration (NMPA) approved the drug for relapsing forms of multiple sclerosis (RMS) for adults and children 10 years and older.

The product remains a revenue powerhouse for Swiss giant Novartis (NOVN: VX), bringing in several billion dollars per year, and the firm has been eager to both  defend and  broaden market share, as the sunset years of its patent estate approach.

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 Pharmaceutical