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).
Sanofi (EURONEXT: SAN and NYSE: SNY) announced today the inauguration of a new assembling and packaging line to produce its flagship pre-filled insulin injection pen Lantus® SoloSTAR® at its Beijing plant located at the Beijing Economic-Technological Development Area (BDA).
Sanofi (EURONEXT: SAN and NYSE: SNY) and Regeneron Pharmaceuticals, Inc. (NASDAQ: REGN) today announced additional positive results from a Phase 2 trial of SAR236553/REGN727 in patients with heterozygous familial hypercholesterolemia (heFH). SAR236553 / REGN727 is a subcutaneously administered, fully-human antibody targeting PCSK9 in clinical development.
Sanofi (EURONEXT: SAN and NYSE: SNY) announced today abstracts spanning the company’s innovative marketed and late-stage development compounds will be featured at the 2012 American Society of Clinical Oncology Annual Meeting in Chicago, Ill., June 1-5. Sanofi products are noted in more than 170 abstracts to be presented at the meeting.
Idag lanseras Parkguiden – en ny gratisapp för iPhone, Android och surfplattor som guidar besökare till parker runt om i Sverige. Via appen får användare tips och aktuell information om en mängd parker. Dessutom finns pollenprognos- och ”sök närmsta apotek”-funktioner. Parkguiden lanseras av Sanofi med Allegra (fexofenadin), ett receptfritt allergiläkemedel.
Sanofi (EURONEXT: SAN and NYSE: SNY) and its subsidiary Genzyme announced today that the Food and Drug Administration (FDA) and the European Medicines Agency (EMA) have approved a second operation for filling and finishing product at its Waterford, Ireland manufacturing plant.
Nu lanseras varumärket Allegra (fexofenadin). Ett receptfritt läkemedel mot säsongsbundna pollenallergier. Nästan var tredje person i Sverige lider av allergier. En tredjedel av dessa personer behandlar inte sina allergier och många pollenallergiker stannar inomhus de dagar då de har besvär. Allegra har en påbörjad effekt inom en timme och ger mindre trötthet än andra äldre antihistaminer.
Läkemedelsföretaget Sanofi presenterar idag Diabetesrapporten 2011. Den visar på stora regionala skillnader i måluppfyllelsen mellan olika landsting. Rapporten visar också att endast var fjärde av landets patienter som behandlas med tabletter och insulin når det uppsatta blodsockervärdet. För högt långtidsblodsocker (HbA1c) ökar risken för hjärtinfarkt, stroke samt dialyskrävande njursjukdom.
Europeisk förskrivarinformation har uppdaterats för att säkerställa att MULTAQ® används till lämpliga patienter med paroxysmalt och persisterande förmaksflimmer. CHMP vid EMA har bekräftat att en positiv nytto-riskbalans för MULTAQ® kvarstår vid behandling av en begränsad population av patienter med paroxysmalt och persisterande förmaksflimmer, efter sin granskning i enlighet med EMA:s artikel 20.
Over 2012-2015, Sanofi expects to deliver sales growth of at least 5% on average and higher business EPS growth. Growth platforms and Genzyme expected to provide more than 80% of Group sales in 2015. Solid progress on R&D transformation with the potential to launch 19 projects by end of 2015.
Sanofi arrangerade i år två seminarier om patientens rätt till livsförlängande behandling i vården, med fokus på cancer och prostatacancer. Se webb-tv reportaget från våra seminarier.