Galderma’s Nemluvio wins eczema nod from FDA
Switzerland’s Galderma (SWX: GALD) has won US Food and Drug Administration (FDA) approval for the use of Nemluvio (nemolizumab) for patients aged 12 years and older with moderate-to-severe atopic dermatitis (AD), alongside topical corticosteroids (TCS) and/or calcineurin inhibitors (TCI), when the disease is not adequately controlled with topical prescription therapies.
This follows the FDA approval of Nemluvio for subcutaneous injection for the treatment of adults with prurigo nodularis in August 2024.
AD - also known as eczema - affects more than 230 million people worldwide, impacting approximately 7% of people in the USA.
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