Amgen Submits Supplemental NDA for Mild-to-Moderate Psoriasis Drug Otezla

Amgen Submits Supplemental NDA for Mild-to-Moderate Psoriasis Drug Otezla

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Amgen has submitted a supplemental New Drug Application (sNDA) to the U.S. Food and Drug Administration (FDA) for its adult mild-to-moderate plaque psoriasis treatment, Otezla® (apremilast), according to a statement released by the company today.