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    DGAP-Adhoc  599  0 Kommentare Teprotumumab Restarts Clinical Development in New Indication


    Genmab A/S

    11.06.2013 21:54

    Dissemination of a Adhoc News, transmitted by DGAP - a company of EQS Group
    AG.
    The issuer is solely responsible for the content of this announcement.

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    Company Announcement

    -- Teprotumumab (RG1507) to be investigated for new indication
    -- River Vision Development Corporation to conduct clinical development under
    a license from Roche

    Copenhagen, Denmark; June 11, 2013 - Genmab A/S (OMX: GEN) announced today that
    teprotumumab (RG1507), an antibody developed by Genmab under our collaboration
    with Roche, will restart clinical development in a Phase 2 study in patients
    with active thyroid eye disease. Clinical development will be conducted by
    River Vision Development Corporation, who licensed teprotumumab from Roche.

    'In drug development, it's often possible to take what was learned about a
    product in its initial development and apply it to new indications. We are
    pleased that River Vision will resume clinical development of teprotumumab for
    the potential treatment of ophthalmic conditions,' said Jan van de Winkel,
    Ph.D., Chief Executive Officer.

    Under our collaboration with Roche, Genmab will receive milestones as well as
    royalty payments on successful products.

    River Vision Development Corporation is a private company focused on
    ophthalmology.

    Today's news does not affect Genmab's financial guidance for 2013.

    About Teprotumumab
    Teprotumumab is a fully human antibody that targets the Insulin-like Growth
    Factor-1 Receptor (IGF-1R) which is a well validated target. Teprotumumab was
    previously investigated in various cancer indications.

    About Genmab A/S
    Genmab is a publicly traded, international biotechnology company specializing
    in the creation and development of differentiated human antibody therapeutics
    for the treatment of cancer. Founded in 1999, the company's first marketed
    antibody, ofatumumab (Arzerra(r)), was approved to treat chronic lymphocytic
    leukemia in patients who are refractory to fludarabine and alemtuzumab after
    less than eight years in development. Genmab's validated and next generation
    antibody technologies are expected to provide a steady stream of future product
    candidates. Partnering of innovative product candidates and technologies is a
    key focus of Genmab's strategy and the company has alliances with top tier
    pharmaceutical and biotechnology companies. For more information visit
    www.genmab.com.

    Contact:
    Rachel Curtis Gravesen, Senior Vice President, Investor Relations &
    Communications
    T: +45 33 44 77 20; M: +45 25 12 62 60; E: r.gravesen@genmab.com
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    DGAP-Adhoc Teprotumumab Restarts Clinical Development in New Indication Genmab A/S 11.06.2013 21:54 Dissemination of a Adhoc News, transmitted by DGAP - a company of EQS Group AG. The issuer is solely responsible for the content of this …

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