NEJM publishes data on Gilenya in pediatric multiple sclerosis

13 September 2018
novartis-big

Swiss pharma giant Novartis (NOVN: VX) has published full results from the Phase III Gilenya (fingolimod) PARADIGMS study in the New England Journal of Medicine (NEJM).

The study, which compared Gilenya with interferon beta-1a in children and adolescents with relapsing forms of MS (RMS), was used to support approval in the USA for an expanded label.

PARADIGMS was conducted in 80 centers in 25 countries, and was designed with input from the US Food and Drug Administration and the European Medicines Agency.

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