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    FDA grants rezafungin QIDP and fast track designations

    Author:
    HT Staff
    Publish date: September 28, 2018

    The U.S.

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    News

    Factors that may drive relapse in AYAs with ALL

    Author:
    HT Staff
    Publish date: September 27, 2018

    New research suggests race, clinical trial participation, and treatment duration may influence the risk of relapse in adolescents and young adults...

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    Study supports immediate compression after DVT

    Author:
    HT Staff
    Publish date: September 27, 2018

    Immediate compression therapy provides a “clear benefit” for patients with deep vein thrombosis (DVT), according to the senior author of a study...

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    News

    Placenta-derived product receives orphan designation for HSCT

    Author:
    HT Staff
    Publish date: September 27, 2018

    The U.S.

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    FDA lifts partial hold on tazemetostat trials

    Author:
    HT Staff
    Publish date: September 26, 2018

    The U.S.

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    Blinatumomab approved to treat ALL in Japan

    Author:
    HT Staff
    Publish date: September 26, 2018

    The Japanese Ministry of Health, Labour and Welfare has approved blinatumomab (Blincyto®) for the treatment of relapsed or refractory B-cell acute...

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    News

    FDA approves duvelisib for CLL/SLL and FL

    Author:
    HT Staff
    Publish date: September 25, 2018

    The U.S.

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    FLT3 inhibitor approved for rel/ref AML in Japan

    Author:
    HT Staff
    Publish date: September 25, 2018

    The Japanese Ministry of Health, Labour and Welfare (MHLW) has approved the FLT3 inhibitor gilteritinib (Xospata®) to treat patients with FLT3-...

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    News

    Drug approved as part of frontline therapy for HL

    Author:
    HT Staff
    Publish date: September 25, 2018

    The Japanese Ministry of Health, Labour and Welfare has approved brentuximab vedotin (Adcetris) in combination with doxorubicin, vinblastine, and...

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    News

    Product approved to treat hemophilia A in Japan

    Author:
    HT Staff
    Publish date: September 25, 2018

    The Japanese Ministry of Health, Labour and Welfare has approved Jivi® (also known as damoctocog alfa pegol or antihemophilic factor [recombinant...

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    News

    CHMP reconsiders new indication for blinatumomab

    Author:
    HT Staff
    Publish date: September 24, 2018

    The European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) said it will re-examine a recent opinion on blinatumomab (...

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    CHMP backs proposed biosimilars of pegfilgrastim

    Author:
    HT Staff
    Publish date: September 24, 2018

    The European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) has recommended approval for three proposed biosimilars of...

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    News

    CHMP recommends factor VIII therapy for hemophilia A

    Author:
    HT Staff
    Publish date: September 24, 2018

    The European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) has recommended approval for damoctocog alfa pegol, a...

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    News

    CHMP supports new indication for venetoclax

    Author:
    HT Staff
    Publish date: September 23, 2018

    The European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) has recommended that the European Commission (EC) approve a...

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    News

    CHMP recommends mogamulizumab for MF, SS

    Author:
    HT Staff
    Publish date: September 22, 2018

    The European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) has recommended approval for mogamulizumab (Poteligeo)....

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