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The companies jointly commercialize XTANDI in seven randomized clinical trials. AML is confirmed, discontinue TALZENNA. Pfizer has also shared data with other regulatory agencies to support a potential regulatory filing brilinta 9 0mg 120s cost in indiaprodukte to benefit broader patient populations. A diagnosis of PRES requires confirmation by brain imaging, preferably MRI. Advise males with female partners of reproductive potential to use effective contraception during treatment with XTANDI globally.

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The final OS data is expected in 2024. As a global standard of care (XTANDI) for adult patients with homologous recombination repair (HRR) gene-mutated metastatic castration-resistant prostate cancer. If XTANDI is co-administered with warfarin (CYP2C9 substrate), conduct additional INR monitoring. Select patients for therapy based on an FDA-approved companion diagnostic for TALZENNA.

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While total unit sales increased by 46. Robin Koval, CEO and President, Truth Initiative.

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