Safety and antitumor activity of the PARP inhibitor BMN673 in a phase 1 trial recruiting metastatic small-cell lung cancer (SCLC) and germline BRCA-mutation carrier cancer patients.

03 medical and health sciences 0302 clinical medicine 3. Good health
DOI: 10.1200/jco.2014.32.15_suppl.7522 Publication Date: 2019-01-03T22:35:36Z
ABSTRACT
7522 Background: BMN 673 is the most potent inhibitor of PARP1/2 in clinical development (IC50<1nM), inducing synthetic lethality in tumors deficient in homologous recombination. Based on preclinic...
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