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LEO Pharma Announces FDA Acceptance of Supplemental NDA for ANZUPGO® (delgocitinib) Cream for the Treatment of Chronic Hand Eczema in Children Aged 12-17

MADISON, N.J.--(BUSINESS WIRE)--LEO Pharma Inc., a global leader in medical dermatology, today announced that the U.S. FDA accepted its supplemental New Drug Application (sNDA) for ANZUPGO® (delgocitinib) cream for the treatment of pediatric patients aged 12 to 17 years with moderate to severe chronic hand eczema (CHE). ANZUPGO cream is a topical and non-steroidal pan-Janus kinase (JAK) inhibitor currently approved in the U.S. for the treatment of moderate to severe chronic hand eczema (CHE) in

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