Pressmeddelanden

2013-09-18 15:17 CEST Sanofi Cambridge, Massachusetts – 17 september 2013 – Genzyme, ett bolag i Sanofikoncernen (EURONEXT: SAN och NYSE: SNY) meddelade idag att den Europeiska kommissionen har gett marknadsföringstillstånd för Lemtrada™. Detta kommer kort tid efter godkännandet för Aubagio® som tillkännagavs den 30:e augusti. Företaget har som målsättning att snart börja lansera båda produkterna inom EU.

2013-09-04 09:47 CEST Sanofi Cambridge, Massachusetts USA. – 2 september 2013 – Genzyme, ett bolag ägt av Sanofi (EURONEXT: SAN och NYSE: SNY), meddelade idag att den Europeiska kommissionen har godkänt Aubagio® (teriflunomid) 14 mg, ett oralt läkemedel som ska tas en gång om dagen, för behandling av skovvis förlöpande multipel skleros (RRMS, relapsing-remitting MS).

2013-06-28 15:44 CEST Sanofi Cambridge, Mass. – June 28, 2013 – Genzyme, a Sanofi company, announced today that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has issued a positive opinion for approval of LEMTRADA™ (alemtuzumab) for the treatment of adult patients with relapsing remitting multiple sclerosis (RRMS) with active disease defined by clinical or imaging features.

2013-04-25 11:41 CEST Sanofi Sanofi and its subsidiary Genzyme announced today positive top-line results from the TOPIC trial for AUBAGIO (teriflunomide). The trial was designed to assess whether early initiation of AUBAGIO (teriflunomide) in patients who experienced their first neurological symptoms consistent with Clinically Isolated Syndrome can prevent or delay conversion to clinically definite multiple sclerosis (CDMS).

2012-11-01 15:44 CET Sanofi Genzyme, a Sanofi company (EURONEXT: SAN and NYSE: SNY), announced today the publication of results from the LEMTRADA™ (alemtuzumab) CARE-MS I and CARE-MS II pivotal studies in patients with relapsing-remitting multiple sclerosis (MS) in the November 1, 2012, online issue of The Lancet.

2012-10-12 16:41 CEST Sanofi Sanofi and its subsidiary Genzyme announced today that key data from the TOWER trial were presented at the 28th Congress of the European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS).

2012-10-09 15:37 CEST Sanofi Genzyme, a Sanofi company (EURONEXT: SAN and NYSE: SNY), announced today new data from Genzyme’s clinical development programs for AUBAGIO® (teriflunomide) and LEMTRADA TM (alemtuzumab) will be presented at the 28th Congress of the European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS) in Lyon, France, October 10-13.

2012-10-02 15:49 CEST Sanofi Paris, France - October 2, 2012 - Sanofi (EURONEXT: SAN and NYSE: SNY) and its subsidiary Genzyme announced today that ENGAGE, the first Phase 3 trial of its investigational oral therapy, eliglustat tartrate, in previously untreated patients with Gaucher disease type 1, met its primary endpoint.

2012-09-12 09:00 CEST Sanofi Paris, France – September 12, 2012 - Sanofi (EURONEXT: SAN and NYSE: SNY) and its subsidiary Genzyme announced today that the U.S. Food and Drug Administration (FDA) has approved AUBAGIO® (teriflunomide) as a new once-daily, oral treatment indicated for patients with relapsing forms of multiple sclerosis (MS).

2012-08-27 16:19 CEST Sanofi Paris, France - August 27, 2012 - Sanofi (EURONEXT: SAN and NYSE: SNY) and its subsidiary Genzyme announced that Genzyme has received a Refuse to File letter from the U.S. Food and Drug Administration (FDA) in response to the supplemental Biologics License Application (sBLA) for the approval of LEMTRADA™ (alemtuzumab) as a treatment for relapsing multiple sclerosis.