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Last $38.37 USD
Change Today -0.12 / -0.31%
Volume 3.6M
SNY On Other Exchanges
EN Paris
EN Paris
New York
EN Paris
As of 8:04 PM 02/11/16 All times are local (Market data is delayed by at least 15 minutes).
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Company Description

Contact Info

54, Rue La Boétie

Paris, 75008


Phone: 33 1 53 77 40 00

Fax: 33 1 53 77 42 96

n the United States and Japan. Apidra: Apidra (insulin glulisine) is a rapid acting analog of human insulin. Apidra is indicated for the treatment of adults with type 1 or type 2 diabetes for supplementary glycemic control. Apidra could be administered subcutaneously using syringes or specific pens, including the Apidra SoloSTAR disposable pen and the ClikSTAR reusable pen. Apidra is available in approximately 100 countries worldwide. Insuman: Insuman (human insulin) is a range of insulin solutions and suspensions for injection and is indicated for diabetes patients where treatment with insulin is required. Insuman is supplied in vials, cartridges, pre filled disposable pens (OptiSet and SoloSTAR), or reusable pens (ClickSTAR). The Insuman range includes rapid acting insulin solutions (Insuman Rapid and Insuman Infusat) that contain soluble insulin, an intermediate acting insulin suspension (Insuman Basal) that contains isophane insulin, and combinations of fast acting and intermediate acting insulins in various proportions (Insuman Comb). Insuman is principally sold in Germany and emerging markets. Lyxumia: Lyxumia (lixisenatide) is a once daily prandial glucagon-like peptide-1 receptor agonist and is indicated for the treatment of adults with type 2 diabetes mellitus to achieve glycemic control in combination with oral glucose lowering medicinal products and/or basal insulin when these, together with diet and exercise, do not provide adequate glycemic control. In 2013, the European Commission granted marketing authorization in Europe for Lyxumia. The company initiated a phased launch of Lyxumia in various European Union countries. Lyxumia has been approved in approximately 50 countries and launched in approximately 20 countries around the world. Additional Phase IIIb studies are ongoing. BGStar/iBGStar/MyStar Extra: The company and its partner, AgaMatrix, are co-developing intelligent solutions in diabetes care that demonstrate their commitment to simplifying and innovating the diabetes management experience for people with diabetes and healthcare providers. These blood glucose monitoring solutions are exclusive to the company and are designed to be synergistic with the rest of its diabetes treatment portfolio. MyStar Extra provides parameters, which are critical for insulin titration, such as three day fasting blood glucose average, fasting blood glucose trend over the last 10 days, and estimation of the A1C trend. MyStar Extra is available in various European countries, including Italy, Spain, France, Germany, and the United Kingdom. BGStar and iBGStar are available in various European countries (including France, Germany, Spain, Italy, and the United Kingdom), in Canada, and in some other countries, including Brazil. Rare Diseases The company’s Rare Diseases business is focused on products for the treatment of rare genetic diseases and other chronic debilitating diseases, including lysosomal storage disorders (LSDs), a group of metabolic disorders caused by enzyme deficiencies. Cerezyme: Cerezyme (imiglucerase for injection) is an enzyme replacement therapy used to treat Gaucher disease, an inherited, potentially life threatening LSD. Cerezyme reduces, relieves, and reverses majority of the symptoms and risks of Type 1 and Type 3 (in certain markets) Gaucher disease. Cerezyme is administered by intravenous infusion approximately 1 or 2 hours. The principal markets for Cerezyme are the United States, Europe, and Latin America. Cerdelga: Cerdelga (eliglustat) is the first-line oral therapy for Gaucher disease type 1. A potent, highly specific ceramide analogue inhibitor of GL-1 synthesis with tissue distribution, Cerdelga has demonstrated efficacy in patients who switch from enzyme replacement therapy, as well as in untreated patients. The principal market for Cerdelga is the United States. It received European Medicines Agency (EMA) approval in January 2015. Myozyme/Lumizyme: Myozyme/Lumizyme (alglucosidase alpha) are enzyme replacement therapies used to treat Pompe disease, an inherited, progressive and often fatal LSD. Myozyme is marketed the United States and the European Union, and is av


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