Storys zum Thema Economy

Folgen
Keine Story zum Thema Economy mehr verpassen.
Filtern
  • 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 – 17:26

    IMD

    IMD Alumni Club Zurich and Accenture Team Up on UNICEF Pro Bono Consulting Project

    Lausanne (ots) - IMD, one of the world's top business schools, announces that its Zurich Alumni Club and Accenture Zürich, a leading worldwide strategy consultancy, have successfully completed a pro bono consulting project with UNICEF Switzerland (Baumackerstrasse 24, 8050 Zürich), world-renowned supporter of children's causes in the United Nations member ...

  • 06.10.2004 – 17:12

    Eli Lilly and Company

    Number, Severity of Fractures Predict Future Risk

    Indianapolis (ots/PRNewswire) - - New Analysis Showed Teriparatide Prevented Fracture Risk Associated with Increasing Number, Severity of Osteoporotic Fractures Data presented at the American Society for Bone and Mineral Research (ASBMR) 26th annual meeting in Seattle, Wash., showed that the number and severity of prior fractures are strong predictors of future fractures in postmenopausal women with ...

  • 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 ...

  • 05.10.2004 – 23:26

    Robbins & Myers, Inc.

    Robbins & Myers Announces Cash Dividend and Annual Meeting Date

    Dayton, Ohio (ots/PRNewswire) - Robbins & Myers, Inc. (NYSE: RBN) announced today that its Board of Directors approved a regular quarterly cash dividend payment of US $.055 per share that is payable on October 29, 2004 to shareholders of record as of October 15, 2004. The Company also announced that its annual shareholders' meeting will be held December 8, 2004 in Dayton, Ohio, with record date set of October 15, ...

  • 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 ...