Praluent Panel To Focus On Indication Breadth Absent CV Outcomes Data

FDA briefing documents for June 9 advisory committee review of Sanofi/Regeneron's alirocumab reflect concern that PCSK9 inhibitors, which lack long-term cardiovascular outcomes data, will be used in place of statins, an established class of drugs with extensive evidence of clinical benefit and long-term safety.

An FDA advisory committee will meet June 9 to discuss the breadth of indication for Sanofi and Regeneron Pharmaceuticals Inc.'s lipid-lowering injectable agent Praluent (alirocumab), including whether the PCSK9 inhibitor is appropriate for patients purported to be "statin intolerant."

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