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December 6, 2004
Takeda Obtains Approval of Blopress for Treatment of CHF in EUTakeda Pharmaceutical Company announced on November 29 that Takeda Europe Research and Development Centre in the UK, its 100% owened subsidiary, obtained an approval of Blopress (candesartan cilexetil), an ARB…

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Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…

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