- Nytt basinsulin som påvisar god glykemisk kontroll med färre hypoglykemier - Stockholm - April 28, 2015 - Sanofi tillkännagav idag att den Europeiska Kommissionen beviljat marknadsföringstillstånd för Toujeo® (insulin glargin injektion, 300 enheter/ml), nästa generations basinsulin för behandling av typ 1- och typ 2-diabetes hos vuxna.
Stockholm 6 mars 2015 – Sanofi (EURONEXT: SAN och NYSE: SNY) meddelade idag att kommittén för humanläkemedel (CHMP) vid Europeiska läkemedelsmyndigheten (EMA) har utfärdat ett positivt yttrande där man rekommenderar godkännande av Toujeo® (insulin glargin 300 enheter/ml) för behandling av vuxna med typ 1- och typ 2-diabetes.
Under ett Sanofi-sponsrat symposium den 16 januari berättade Professor Brian Frier, Scotland, att hypoglykemier (lågt blodsocker) hos personer med typ 2-diabetes är vanligare än vad man tror. I en nyligen publicerad studie var frekvensen av icke-allvarliga hypoglykemier 0,4-0,7 episoder/patient och vecka .
EURONEXT: SAN and NYSE: SNY announced today that the first phase 3 study results for its investigational new insulin U300 showed equivalent blood sugar control with fewer night-time low blood sugar events compared to Lantus® (insulin glargine [rDNA origin] injection). The company also announced topline results of a second Phase 3 study (EDITION II) for new insulin.
Sanofi announced today that clinical data highlighting the company’s ongoing commitment to advancing diabetes care will be presented at the American Diabetes Association (ADA) 73rd Scientific Sessions in Chicago, USA. In total, more than 60 abstracts representing new data sets on Sanofi diabetes drugs, investigational drugs or medical devices are part of the official scientific program.
Sanofi (EURONEXT: SAN and NYSE: SNY) announced today thatthe Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency(EMA) has issued a positive opinion for inclusion in the Lantus® (insulin glargine) product label of safety and efficacy data from the insulin glargine cardiovascular (CV) outcomes trial ORIGIN(Outcome Reduction with Initial Glargine INtervention).
Sanofi lanserar ny behandling: den första prandiella GLP-1 receptoragonisten, som tas en gång per dag i samband med måltid
Sanofi meddelade idag att kommittén för humanläkemedel (CHMP) vid Europeiska läkemedelsmyndigheten (EMA) har utfärdat ett positivt yttrande där man rekommenderar godkännande av Lyxumia ® (lixisenatid) en gång dagligen för behandling av vuxna med typ 2-diabetes för att uppnå glykemisk kontroll i kombination med orala glukossänkande läkemedel och/eller basinsulin.
Sanofi and T1D Exchange, a non-profit organization focused on type 1 diabetes, announced today on World Diabetes Day that they will collaborate on the TEENs registry study. The aim of the study is to provide the type 1 diabetes community with a better understanding of how children, adolescents and young adults are currently living with type 1 diabetes.
Paris, France – October 5, 2012 – Sanofi (EURONEXT: SAN and NYSE: SNY) today announced new results from the landmark ORIGIN trial showing treatment with Lantus® was approximately 3-fold more likely to achieve and maintain target glycemic levels, defined as HbA1C < 6.5% in this analysis, vs. standard care in individuals with pre-diabetes or early type 2 diabetes at high cardiovascular risk.
Sanofi (EURONEXT: SAN and NYSE: SNY) today announced results from a study showing that the mechanism of action of once-daily Lyxumia® (lixisenatide) significantly delayed gastric emptying, a process accompanied by significant post-prandial glucose (PPG) lowering.
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.
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