Publisher
Springer Science and Business Media LLC
Reference43 articles.
1. Clovis Oncology Inc. Prescribing information for RubracaTM (rucaparib) tablets, for oral use. 2016. http://www.fda.gov . Accessed 9 Jan 2017.
2. Jenner ZB, Sood AK, Coleman RL. Evaluation of rucaparib and companion diagnostics in the PARP inhibitor landscape for recurrent ovarian cancer therapy. Future Oncol. 2016;12(12):1439–56.
3. Swisher EM, Lin KK, Oza AM, et al. Rucaparib in relapsed, platinum-sensitive high-grade ovarian carcinoma (ARIEL2 Part 1): an international, multicentre, open-label, phase 2 trial. Lancet Oncol. 2017;18(1):75–87.
4. Plummer R, Lorigan P, Steven N, et al. A phase II study of the potent PARP inhibitor, rucaparib (PF-01367338, AG014699), with temozolomide in patients with metastatic melanoma demonstrating evidence of chemopotentiation. Cancer Chemother Pharmacol. 2013;71(5):1191–9.
5. Clovis Oncology Inc. Clovis Oncology, Inc. receives license for worldwide development and commercialization rights to Pfizer’s oral and IV PARP inhibitor PF-01367338 [media release]. 2011. http://www.clovisoncology.com .
Cited by
71 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献