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Live News REGULATION ARTICLE M impact

FDA Accepts Biohaven’s Resubmitted Drug Application for Review

Biohaven said the FDA accepted its resubmitted New Drug Application for an experimental rare-disease drug.

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By Mackenzie TatananniBiohaven stock was having its best day in three years after the Food and Drug Administration agreed to review a resubmitted application for the biotech's experimental rare-disease drug.Biohaven disclosed Thursday that U.S. regulators accepted a New Drug Application (NDA) resub…