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Galderma’s Nemluvio® (Nemolizumab) Granted Marketing Authorization in the United Kingdom and Switzerland for Moderate-to-Severe Atopic Dermatitis and Prurigo Nodularis

ZUG, Switzerland, February 18, 2025--Galderma today announced that the United Kingdom (UK) Medicines and Healthcare products Regulatory Agency and Swissmedic have granted the marketing authorization of nemolizumab for the treatment of both atopic dermatitis and prurigo nodularis in the UK and Switzerland, respectively. Specifically, the approvals are for nemolizumab’s subcutaneous use for the treatment of moderate-to-severe atopic dermatitis in combination with topical corticosteroids and/or cal

articleGalderma Group AgFebruary 18, 20257/company/galderma-group-n/news/galderma-nemluvio-nemolizumab-granted-marketing-060000998
Galderma’s Nemluvio® (Nemolizumab) Granted Marketing Authorization in the United Kingdom and Switzerland for Moderate-to-Severe Atopic Dermatitis and Prurigo Nodularis

About this update from Galderma Group Ag

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atopic dermatitisprurigo nodularisSwitzerlandAccess Consortiumsystemic therapytreatment optionnemolizumabpatientsUnited Kingdomnovel treatment