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    DGAP-News  707  0 Kommentare WILEX AG: Phase III ARISER data for the adjuvant treatment of clear cell renal cancer with RENCAREX(R) including retrospective subgroup analysis presented at ASCO - Seite 3


    on 4 June 2013 at 3:00 p.m. CET in English. Please dial in ten minutes
    before the conference call using the following dial-in numbers:

    1. Germany: +49 69 71044 5598
    2. UK: +44 20 3003 2666
    3. USA: +1 212 999 6659
    4. USA Freephone: +1 866 966 5335

    You will be welcomed by an operator taking your name and company. The
    presentation slides for the conference will be available for download at
    www.wilex.de on 04 June 2013 at 2:30 p.m. CET.

    About RENCAREX(R) and the ARISER study
    The drug candidate RENCAREX(R) is based on the antibody Girentuximab, which
    binds to the tumour-specific antigen CAIX - an antigen that is
    overexpressed in clear cell renal cell carcinomas (ccRCC).

    ARISER (Adjuvant RENCAREX(R) Immunotherapy trial to Study Efficacy in
    non-metastasised Renal cell carcinoma) was an international, multicentre,
    randomised Phase III trial that examined the efficacy of the antibody
    RENCAREX(R) in comparison to placebo in the treatment of clear cell renal
    cell cancer patients following complete or partial surgical removal of the
    affected kidney in patients with no detectable metastases but at high risk
    of recurrence. The study enrolled 864 patients that had had prior
    nephrectomy of primary RCC no later than 12 weeks before study entry with
    documented clear cell histology, an ECOG score of 0 or 1 and no evidence of
    macroscopic or microscopic residual disease. Under the treatment schedule
    patients received a once-weekly infusion of RENCAREX(R) or placebo (50:50)
    for 24 weeks. Patients receiving RENCAREX(R) were dosed at 50 mg in the
    first week followed by weekly doses of 20 mg during weeks 2-24.

    RENCAREX(R) has Fast Track designation for ccRCC in the USA and Orphan Drug
    designation for RCC in the USA and EU.

    About WILEX
    WILEX AG is a biopharmaceutical company based in Munich, Germany. Focused
    on oncology, the Company develops diagnostic and therapeutic product
    candidates for the specific detection and targeted treatment of various
    types of cancer. In the field of therapeutics, WILEX develops small
    molecules (MESUPRON(R) two Phase IIa trials completed, WX-554 in Phase
    Ib/II and WX-037 in preclinical development). In the field of diagnostics,
    REDECTANE(R) is an antibody-based imaging in vivo diagnostic agent that is
    currently in a Phase III programme. The Company also has a portfolio of
    research use only tests and in vitro diagnostic agents that are marketed
    via its US subsidiary WILEX Inc. in Cambridge, MA, under the brand Oncogene
    Science. WILEX's subsidiary Heidelberg Pharma GmbH offers preclinical
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    DGAP-News WILEX AG: Phase III ARISER data for the adjuvant treatment of clear cell renal cancer with RENCAREX(R) including retrospective subgroup analysis presented at ASCO - Seite 3 DGAP-News: WILEX AG / Key word(s): Research Update WILEX AG: Phase III ARISER data for the adjuvant treatment of clear cell renal cancer with RENCAREX(R) including retrospective subgroup analysis presented at ASCO 03.06.2013 / …