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olaparib

Known as: 4-(3-{[4-(cyclopropylcarbonyl)piperazin-1-yl]carbonyl}-4-fluorobenzyl)phthalazin-1(2H)-one 
A substance being studied in the treatment of breast, ovarian, and prostate cancers caused by mutations (changes) in the BRCA1 and BRCA2 genes. It is… 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
6003Background: Combination cediranib (C) and olaparib (O) improved progression-free survival (PFS) in patients (pts) with… 
2019
2019
5507 Background: The CLIO trial (NCT02822157) evaluated olaparib single-agent therapy versus standard of care chemotherapy in… 
Highly Cited
2016
Highly Cited
2016
5500 Background: Olaparib (AZD2281; KU-0059436) is a novel, orally active PARP inhibitor that induces synthetic lethality in… 
2014
2014
Indoleamine 2,3-dioxygenase-1 (IDO) is an immunosuppressive molecule expressed by most human tumors. IDO levels correlate with… 
2013
2013
A series of setbacks almost caused the demise of PARP inhibitors, but four companies are now beginning pivotal trials of these… 
2013
2013
5505 Background: Previously, we reported that maintenance treatment with the oral PARP inhibitor olaparib (400 mg bid) led to a… 
Highly Cited
2012
Highly Cited
2012
Background:Olaparib (AZD2281) is a potent oral poly(ADP-ribose) polymerase inhibitor with anti-tumour activity and acceptable… 
2011
2011
A continuing quest in clinical oncology is to effectively eliminate tumors without major side effects. But drugs rationally…