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FDA Delays Action On MedImmune's Rezield Despite Negative Panel Vote

This article was originally published in Pharmaceutical Approvals Monthly

Executive Summary

In a surprise move, FDA has delayed action on MedImmune's Rezield (motavizumab), its second-generation preventive treatment for respiratory syncytial virus, even though the agency already has a vote against approval from an overwhelmingly negative advisory committee review three weeks earlier

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