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  • 07.10.2004 – 08:30

    Zeltia Group

    The FDA has Granted Orphan Drug Status to Yondelis for the Treatment of STS

    Madrid (ots/PRNewswire) - The United States Food & Drug Administration (FDA) has granted Orphan Drug Designation to Yondelis in the indication of Soft Tissue Sarcoma (STS). The sponsor of this application in the US is our partner Johnson & Johnson Pharmaceutical Research & Development. The European Commission (E.C.) already granted Orphan Drug status for this ...

  • 06.10.2004 – 08:43

    Zeltia Group

    FDA Grants Aplidin(R) Orphan Drug Status for the Treatment of Multiple Myeloma

    Madrid, Spain (ots/PRNewswire) - PharmaMar announced today that Aplidin(R), its second marine-derived compound in Phase II clinical development, has been granted orphan drug status by the United States (US) Food and Drug Administration (FDA), for the treatment of Multiple Myeloma (MM). This is the second orphan drug designation granted to Aplidin by the FDA. The ...

  • 24.09.2004 – 23:47

    ProMetic Life Sciences

    ProMetic Modifies its Organisational Structure

    Montreal (ots/PRNewswire) - ProMetic Life Sciences (PLI:TSX) announced today the administrative reorganisation of its communications and business development structure. By implementing these changes, the Company is focusing its business development activities in key markets providing optimal growth opportunities namely in the United States, Europe, Asia and the Middle East. ProMetic can better achieve this goal ...

  • 22.09.2004 – 14:14

    Prionics AG

    European Biotech Award goes to Swiss-based Prionics

    Zurich (ots) - The Swiss-based company Prionics AG has won the most highly acclaimed European Biotech Award, the European Biotechnica Award for Excellence in Biotech Business. The award was handed over yesterday at the Biotechnica Business Forum in Berlin by the German Federal Minister of Economic Affairs, Wolfgang Clement. The international jury awarded the Biotech prize for Prionics' excellent track record both ...

  • 01.09.2004 – 11:20

    Genmab A/S

    T-Cell Lymphoma Patients Achieve Long Lasting Responses With Genmab's HuMax-CD4

    Copenhagen, Denmark (ots/PRNewswire) - Genmab A/S (CSE: GEN) announced today that cutaneous T-cell lymphoma (CTCL) patients in the HuMax-CD4 Phase II studies achieved long lasting responses, with an average response duration of more than 6.6 months. This duration of response data is based on an analysis of responding mycosis fungoides (MF) patients at all dose ...

  • 26.08.2004 – 07:32

    Roche Holding AG

    New Hope in Fight Against Advanced Lung Cancer

    Basel, Switzerland (ots/PRNewswire) - - Roche files marketing application for Tarceva with European health authorities Roche today submitted a Marketing Authorisation Application to the European health authorities for its new cancer drug Tarceva (erlotinib) for the treatment of advanced non-small cell lung cancer (NSCLC). NSCLC is the most common form of lung cancer, which in itself is the most frequent cancer ...

  • 23.08.2004 – 10:36

    Novartis International AG

    FDA Approves Zelnorm as the First Rx Therapy for Chronic Constipation

    Basel, Switzerland (ots/PRNewswire) - - 4.5 Million Americans Suffer from Constipation Most of the Time Novartis Pharma AG announced that the U.S. Food and Drug Administration (FDA) today approved a supplemental indication for its pro-motility agent Zelnorm(R) (tegaserod maleate) for the treatment of chronic idiopathic constipation in male and female ...

  • 19.08.2004 – 14:11

    Inion Ltd

    Inion Receives FDA Clearance for Trinion Meniscus Screw

    Tampere, Finland (ots/PRNewswire) - Inion, one of the leading companies in the field of developing biodegradable medical implants, announces FDA 510(k) clearance of its Trinion(TM) Meniscus Screw for use in knee cartilage repair. This clearance allows Inion's Trinion(TM) screws to be marketed and sold in the US, complementing the previously offered HexalonTM biodegradable cruciate ligament repair screw, in the world's ...