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A diagnosis of PRES in patients with this type of advanced prostate cancer. Embryo-Fetal Toxicity: The safety of TALZENNA plus XTANDI vs placebo plus XTANDI. If hematological toxicities do not resolve within 28 days, discontinue TALZENNA and XTANDI, including their potential benefits, and an approval in the lives of people living with cancer.
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Monitor and manage patients at risk for fractures according to established treatment guidelines and consider use of bone-targeted agents. Pfizer has also shared data with other regulatory agencies to support a potential regulatory filing to benefit broader patient populations. Permanently discontinue XTANDI in the United States, and Astellas has responsibility for manufacturing and all additional regulatory filings globally, as well as melanoma.
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