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).
Stockholm – 3 september 2012 – Sanofi meddelar idag att Anna-Kaija Grönblad efterträder Laurent Dousset som vd för Sanofi Sverige. Hon kommer samtidigt att bli divisionschef för onkologi i Norden och Baltikum. Laurent Dousset går vidare till en ny position på huvudkontoret i Paris.
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.
Sanofi and Regeneron Pharmaceuticals, Inc. (NASDAQ: REGN) today announced that the U.S. Food and Drug Administration (FDA) approved ZALTRAP® (ziv-aflibercept) Injection for Intravenous Infusion, in combination with 5-fluorouracil, leucovorin, irinotecan (FOLFIRI), for patients with metastatic colorectal cancer that is resistant to or has progressed following an oxaliplatin-containing regimen.
Sanofi (EURONEXT: SAN and NYSE: SNY) and the Joslin Diabetes Center, a teaching and research affiliate of Harvard Medical School, today announced a new collaboration to promote the development of new medicines for the treatment of diabetes and related disorders. The collaboration was unveiled at the 2012 Bio International Convention in Boston, Mass.
Sanofi (EURONEXT: SAN and NYSE: SNY) announced today that it was granted the award for “Leading Pan-European Quoted Company for Investor Relations” in the 2012 Thomson Reuters Extel Survey. Considered the leading benchmark for excellence in Investor Relations (IR), the survey highlights achievement across companies listed in Europe.
Den internationella studien ORIGIN (Outcome Reduction with Initial Glargine Intervention) har undersökt om det går att förhindra eller skjuta upp kardiovaskulära händelser som kan följa av typ 2-diabetes och om man kan förhindra utvecklingen av typ 2-diabetes hos personer som riskera få denna sjukdom, genom att behandla med Lantus® (insulin glargin) på ett tidigare stadium än vad som görs idag.
Sanofi (EURONEXT: SAN and NYSE: SNY) and its subsidiary Genzyme today announced that the company has submitted a supplemental Biologics License Application (sBLA) to the U.S. Food and Drug Administration (FDA) and a marketing authorization application (MAA) to the European Medicines Agency (EMA) seeking approval of LEMTRADA™ (alemtuzumab) for treatment of relapsing multiple sclerosis (RMS).
Sanofi (EURONEXT: SAN and NYSE: SNY) today announced new results of a large-scale epidemiological program, conducted by independent researchers in the northern European countries, at Kaiser Permanente in Northern and Southern California, and at the University of North Carolina in the United States.
Sanofi (EURONEXT : SAN and NYSE : SNY) announced today that people with early type 2 diabetes uncontrolled on metformin demonstrated superior HbA1c - glycated hemoglobin - reduction with Lantus® (insulin glargine [rDNA origin] injection) versus sitagliptin. These data from the EASIE study were presented at the American Diabetes Association 72nd Scientific Sessions.
Sanofi presenterar studieresultat från prövningsprogrammet GetGoal som visar att lixisenatid, som tillägg till basinsulin och perorala diabetesläkemedel, signifikant sänker långtidsblodsockret (HbA1c) både hos de patienter med typ 2-diabetes som nyligen har påbörjat sin behandling med insulin, och hos de patienter som har behandlats med insulin en längre tid (i genomsnitt 3,1 år).
Sanofi (EURONEXT: SAN and NYSE: SNY) and its subsidiary Genzyme announced today top-line results from the TOWER (Teriflunomide Oral in people With relapsing remitting multiplE scleRosis) trial that assessed the efficacy and safety of once-daily, oral teriflunomide in patients with relapsing forms of multiple sclerosis (MS).
