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FDA watchers would be shocked if US regulators declined to approve the first two applications for proprotein convertase subtilisin/kexin 9 (PCSK9) inhibitors –Sanofi's and Regeneron Pharmaceuticals' Praluent (alirocumab), which is up first, with an action date of 24 July, and Amgen's Repatha (evolocumab), whose verdict is anticipated by 27 August.
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