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FDA CRDAC: Novartis' serelaxin not ready for prime time

This article was originally published in Scrip

Executive Summary

Advisers to the FDA were solidly unanimous in rejecting Novartis' serelaxin (RLX030), a relaxin receptor agonist, as a treatment for acute heart failure (AHF) at a 27 March meeting, which at one point got downright prickly between one of the panelists and the drug maker's key outside expert consultant, who often shares a seat on the same committee.



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