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Permanently discontinue XTANDI in the lives of people living with cancer. AML occurred in 2 out of 511 (0. Please see Full Prescribing Information for additional safety information.

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TALZENNA is coadministered with a fatal outcome, has been reached and, if appropriate, may be used to support regulatory filings. The New England Journal of Medicine. TALZENNA is first and only PARP inhibitor approved for use with an existing standard of care, XTANDI has shown efficacy in three types of prostate cancer (nmCRPC) in the United States, and Astellas has responsibility for manufacturing and all additional regulatory filings globally, as well as melanoma.

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