GDF-15 AS A HAEMATOLOGICAL TOXICITY BIOMARKER

    公开(公告)号:US20210247383A1

    公开(公告)日:2021-08-12

    申请号:US17156002

    申请日:2021-01-22

    Applicant: NOVARTIS AG

    Abstract: The present disclosure relates to use of GDF-15 as a safety biomarker for determining a toxicological effect of a Mdm2 inhibitor; an ex vivo method for determining a toxicological effect of a Mdm2 inhibitor in a subject, in particular for determining a likelihood of developing thrombocytopenia in a subject in response to administration of a dose of a Mdm2 inhibitor; methods of using a Mdm2 inhibitor in the treatment of cancer in a subject; a kit for use in predicting the likelihood that a patient having cancer will develop thrombocytopenia in response to a treatment with a dose of a Mdm2 inhibitor; a kit for use in treating a patient having cancer and related disclosure embodiments.

    GDF-15 as a Haematological Toxicity Biomarker

    公开(公告)号:US20180224431A1

    公开(公告)日:2018-08-09

    申请号:US15749544

    申请日:2016-08-03

    Applicant: NOVARTIS AG

    Abstract: The present disclosure relates to use of GDF-15 as a safety biomarker for determining a toxicological effect of a Mdm2 inhibitor; an ex vivo method for determining a toxicological effect of a Mdm2 inhibitor in a subject, in particular for determining a likelihood of developing thrombocytopenia in a subject in response to administration of a dose of a Mdm2 inhibitor; methods of using a Mdm2 inhibitor in the treatment of cancer in a subject; a kit for use in predicting the likelihood that a patient having cancer will develop thrombocytopenia in response to a treatment with a dose of a Mdm2 inhibitor; a kit for use in treating a patient having cancer and related disclosure embodiments.

    GDF-15 AS A HAEMATOLOGICAL TOXICITY BIOMARKER

    公开(公告)号:US20210255166A1

    公开(公告)日:2021-08-19

    申请号:US17155985

    申请日:2021-01-22

    Applicant: NOVARTIS AG

    Abstract: The present disclosure relates to use of GDF-15 as a safety biomarker for determining a toxicological effect of a Mdm2 inhibitor; an ex vivo method for determining a toxicological effect of a Mdm2 inhibitor in a subject, in particular for determining a likelihood of developing thrombocytopenia in a subject in response to administration of a dose of a Mdm2 inhibitor; methods of using a Mdm2 inhibitor in the treatment of cancer in a subject; a kit for use in predicting the likelihood that a patient having cancer will develop thrombocytopenia in response to a treatment with a dose of a Mdm2 inhibitor; a kit for use in treating a patient having cancer and related disclosure embodiments.

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