Nyhetsarkiv

  • Sanofi-aventis concludes €10 billion in medium-term credit agreements with its banks to refinance the aventis acquisition financing entered into in April 2004

    Sanofi-aventis announced today the simultaneous signature of a medium-term syndicated credit agreement amounting to €8 billion and four bilateral credit facilities amounting to €500 million each. The syndicated credit agreement consists of two revolving credit lines each having a different maturity: • a €5.5 billion five-year tranche with the possibility of extending the maturity up to seven

  • RESCHEDULING OF THE PRE-TRIAL ORDER DATE IN THE UNITED STATES PLAVIX® LITIGATION

    Today sanofi-aventis announced that, at the request of sanofi-aventis, Apotex, and their respective affiliates, the U.S. District Court for the Southern District of New York has approved an extension of the date for submission by the parties of the pre-trial order in its Plavix® patent-infringement litigation with Apotex and Dr. Reddy’s Laboratories. The new date is May 13, 2005. The submission

  • Sanofi-aventis joins the fight against tuberculosis in South Africa

    in partnership with the Nelson Mandela Foundation and the South African Department of Health THE TB FREE PROGRAM for the treatment of tuberculosis sufferers In Johannesburg today, South African Health Minister Dr. Manto Tshabalala-Msimang and sanofi-aventis Chairman and CEO Jean-François Dehecq inaugurated the first training center in support for patients receiving treatment for tuberculosi

  • COURT GRANTS SANOFI-AVENTIS'S REQUEST FOR ORDER OF PROHIBITION IN THE CANADIAN PLAVIX®LITIGATION

    The Canadian Federal Court of Ottawa has granted sanofi-aventis’s application for an order of prohibition against the Minister of Health and Apotex Inc. in relation to Apotex’s 2003 application in Canada for a marketing authorization for a generic version of clopidogrel bisulfate tablets. The Canadian Court rejected Apotex's challenge to the Plavix® patent and held that the asserted claims are nov

  • FDA Advisory Panel Recommends Licensure of sanofi pasteur’s ADACEL™ Vaccine for Combined Protection against Tetanus, Diphtheria and Pertussis

    – Vaccine Leader Looks to Introduce First Pertussis Booster for Both Adolescents and Adults in United States Sanofi pasteur, the vaccines business of the sanofi-aventis Group (NYSE: SNY), announced today that the Vaccines and Related Biological Products Advisory Committee (VRBPAC) of the U.S. Food and Drug Administration (FDA) voted unanimously to recommend licensure of ADACEL™ (Tetanus Toxoi

  • Sanofi Pasteur seeks to broaden age group for new vaccine, Menactra™, to protect against meningococcal disease

    Submits supplemental license application Sanofi Pasteur, the vaccines business of the sanofi-aventis Group, is seeking U.S. government approval to broaden the age indication for its new meningococcal vaccine Menactra™ (Meningococcal [Groups A, C, Y and W-135] Polysaccharide Diphtheria Toxoid Conjugate Vaccine). The company has filed a supplemental application with the U.S. Food and Drug Adminis

  • Sanofi-aventis sues Novopharm for patent infringement in Canada

    Sanofi-aventis has learned through the Canadian Ministry of Health website that Novopharm Limited had obtained marketing approval in Canada for a product claiming to be generic enoxaparin. Sanofi-aventis companies Aventis Pharma Inc. and Aventis Pharma S.A. are bringing suit in the Federal Court against Novopharm for patent infringement of Canadian patent 2045433, which covers Lovenox®. Sanofi

  • Clopidogrel improved coronary perfusion and reduced mortality in acute heart attack

    Results from two major clinical trials presented at ACC (PARIS and PRINCETON, NJ, MARCH 9, 2005) – Results of two major clinical trials showed that the antiplatelet agent clopidogrel, given on top of standard therapy, provided significant benefits to patients with acute ST-segment elevation myocardial infarction (STEMI), a certain kind of heart attack. Results of the COMMIT/CCS-2 (ClOpidogrel

  • Sanofi Aventis och Pfizer seek approval to market Exubera® in the United States

    Pfizer Inc. and the sanofi-aventis Group announced today that the United States Food and Drug Administration (FDA) has accepted for filing a new drug application for Exubera® (inhaled human insulin powder). Exubera®, a dry powder form of insulin that is inhaled into the lungs prior to eating, using a specially designed inhalation device, has been studied in more than 3,500 patients, some for o

  • Personalförändring i sanofi-aventis

    Tommy Olin, commercial operations director, med ansvar för sanofi-aventis sälj- och marknadsorganisation har valt att lämna företaget för att gå vidare i en ny karriär utanför organisationen. Han lämnar sanofi-aventis vid månadsskiftet. För ytterligare information kontakta Annette Hedman, tf informationsanvarig, 08-470 18 52 eller 070-289 88 64. Koncernen sanofi-aventis är det tredje störst

  • Sanofi-aventis receives FDA approval for new Eloxatin® formulation

    Sanofi-aventis announced today that he has received marketing approval from the United States Food and Drug Administration for a new formulation of Eloxatin® (oxaliplatin for injection). This new formulation, Eloxatin® INJECTION, is a clear, preservative-free, colorless solution which does not require reconstitution. Eloxatin® INJECTION offers additional benefit and convenience to physicians an

  • Studies demonstrate significant benefit of Eloxatin

    TWO STUDIES DEMONSTRATE SIGNIFICANT BENEFIT OF ELOXATIN– BASED CHEMOTHERAPY COMBINED WITH BEVACIZUMAB IN ADVANCED COLORECTAL CANCER Positive Results of TREE-2 and ECOG 3200 Trials Presented at the 2005 Gastrointestinal Cancers Symposium in Hollywood, Florida Sanofi-aventis (NYSE: SNY) announced today preliminary results of two large prospective trials evaluating the safety and efficacy of E

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