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Published in 2019 at "Blood"
DOI: 10.1182/blood-2019-131331
Abstract: Introduction KRT-232 is a potent and selective, targeted small molecule inhibitor of human mouse double minute 2 (MDM2) homolog interactions with tumor protein 53 (p53). MDM2 prevents p53 activation and reduces p53-mediated transcription and cell…
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Keywords:
inhibitor;
solid tumors;
mdm2;
multiple myeloma ... See more keywords
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Published in 2020 at "Blood"
DOI: 10.1182/blood-2020-135985
Abstract: Background: KRT-232 is a potent, selective, orally available, small-molecule drug that binds to mouse double minute 2 homolog (MDM2) and inhibits its interactions with tumor suppressor protein p53. KRT-232 is under development for treatment of…
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Keywords:
company;
current employment;
current equity;
krt 232 ... See more keywords
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Published in 2020 at "Blood"
DOI: 10.1182/blood-2020-135987
Abstract: Background: KRT-232 is a potent, selective, orally available, targeted inhibitor of human MDM2 homolog interactions with tumor suppressor protein 53 (p53). KRT-232 is under development for treatment of myeloproliferative neoplasms, acute myeloid leukemia and Merkel…
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Keywords:
drug;
model;
cmax auc0;
ddi ... See more keywords
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1
Published in 2020 at "Journal of Clinical Oncology"
DOI: 10.1200/jco.2020.38.15_suppl.10072
Abstract: 10072Background: MCC is an aggressive neuroendocrine skin cancer with very poor prognosis. Immune checkpoint inhibition was recently shown to benefit some patients (pts). There are few effective tr...
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Keywords:
murine double;
double minute;
class murine;
krt 232 ... See more keywords
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1
Published in 2021 at "Journal of Clinical Oncology"
DOI: 10.1200/jco.2021.39.15_suppl.tps7057
Abstract: TPS7057 Background: The prognosis for patients (pts) with MF who have primary resistance to or who have progressed after treatment with ruxolitinib (RUX) is poor (median OS is ̃13 months), highlighting the unmet need for…
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Keywords:
treatment;
inhibitor;
krt 232;
phase study ... See more keywords