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  1. 147 Posts.
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    Each of the INDIVIDUAL result below - present this and early next week can make VLA be a billion take over target....VLA is worth more than that as it been proven to be effective in multi cancers target.


    Combination of a novel oncolytic immunotherapeutic agent, CAVATAKTM (Coxsackievirus
    A21) and immune-checkpoint blockade significantly reduces tumor growth and improves
    survival in an immune competent mouse melanoma model

    Conclusion:
    The significant anti-tumor activity mediated by the
    combination of CAVATAK and checkpoint inhibitor antibodies
    (anti-PD-1 and anti-CTLA-4) observed in the presented murine
    melanoma model supports clinical evaluation of such an
    immunotherapeutic combination treatment regime in patients
    with advanced melanoma. Clinical evaluation of CAVATAK in
    combination with immune checkpoint blockade in advanced
    melanoma patients is currently underway.


    Phase I/II STORM study: Intravenous delivery of a novel on
    colytic immunotherapy agent,
    CAVATAK, in advanced cancer patients.

    Conclusion:
    To date, multiple IV infusions in advanced cancer
    patients have been generally well tolerated. Initial serum viral
    load data indicate potential tumor-specific CVA21 replication
    in some patients. Overall, the preliminary data offer an exciting
    possibly that tumor targeting, infection and immune activation
    mediated by IV CVA21 may lead to increases in anti-tumor
    activity, particularly when in future used in combination with
    immune checkpoint blockade


    65
    Poster Abstracts
    Oncolytic immunotherapy for the treatment of Non-Muscle Invasive Bladder Cancer using
    intravesical Coxsackievirus A21: Phase I/II CANON study.

    Conclusion:
    CVA21 is an oncolytic virus highly suited for
    application in NMIBC. Modulation of ICAM-1 expression by very
    low doses of mitomycin C facilitates increased virus entry into
    tumour cells. The current phase I/II CANON study is currently
    evaluating neoadjuvant CVA21 in this disease model.

    Oncolytic Virotherapy for the Treatment of Non-Hodgkin Lymphoma

    Conclusions:
    CD54 expression in 5/6 NHL cell lines correlated
    with susceptibility to CAVATAK and increased CD54 expression in
    the LN-like environment potentiated susceptibility to CAVATAK
    in some NHL cell lines at lower doses. Preliminary primary NHL
    sample data shows that CD54 can be detected on B-Cells. These
    results show promise for the use of CAVATAK to treat NHL as it is
    effective against isolated NHL cell lines and those supported by
    interactions within the tumour microenvironment.
 
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