Sun Pharmaceutical Industries announced that the US Food and Drug Administration (FDA) has accepted the New Drug Application (NDA) for deuruxolitinib,
an investigational oral selective inhibitor of Janus kinases JAK1 and JAK2, for the treatment of adults with moderate to severe alopecia areata. In the NDA, Sun Pharma has submitted 8mg twice daily regimen of deuruxolitinib for FDA review.
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