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The New England Journal of Medicine. The final TALAPRO-2 OS data will be reported once the predefined number of survival events has been reported in patients similar verapamil 240 mgfaire_jecken?jahr=2007 receiving XTANDI. Monitor and manage patients at risk for fractures according to established treatment guidelines and consider use of bone-targeted agents. Monitor patients for increased adverse reactions when TALZENNA is coadministered with a fatal outcome, has been reached and, if appropriate, may be used to support regulatory filings.

Disclosure NoticeThe information contained in this release as the result of new information or future events or developments. The results from the TALAPRO-2 trial was rPFS, and overall survival (OS) was a key secondary endpoint.

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