Sanofi’s Aubagio gains backing from UK’s NICE

8 December 2013

In final draft guidance issued on Friday, the UK drugs watchdog the National Institute for Health and Care Excellence (NICE) has recommended the use of French drug major Sanofi (Euronext: SAN) subsidiary Genzyme’s multiple sclerosis drug Aubagio (teriflunomide) for National Health Service use.

The good news came a day after in the NICE called for more information on the company’s Lemtrada (alemtuzumab), also for MS (The Pharma Letter December 6), and follows a call for additional efficacy data from the company (TPL September 18).

NICE is appraising teriflunomide as a treatment for adults with relapsing-remitting multiple sclerosis. This is a chronic, disabling, neurological condition that, as it progresses, can be life altering and has a substantial negative impact on quality of life and activities of daily living.

According to the draft guidance, teriflunomide is recommended for treating adults with active relapsing-remitting multiple sclerosis (normally defined as two clinically significant relapses in the previous two years), only if:

  • they do not have highly active or rapidly evolving severe relapsing-remitting multiple sclerosis; and
  • the manufacturer provides teriflunomide with the discount agreed in the patient access scheme.

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Chairman, Sanofi Aventis UK



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