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
AUTHORS (14)
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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