Dupixent scores a first with China approval for COPD
China’s National Medical Products Administration (NMPA) has approved Dupixent (dupilumab) as an add-on maintenance treatment for adults with uncontrolled chronic obstructive pulmonary disease (COPD) characterized by raised blood eosinophils, French pharma major Sanofi (Euronext: SAN) announced today.
Specifically, the approval covers patients already on a combination of an inhaled corticosteroid (ICS), a long-acting beta2-agonist (LABA) and a long-acting muscarinic antagonist (LAMA), or on a combination of a LABA and a LAMA if ICS is not appropriate.
Dupixent is the first ever biologic medicines to be authorized in China for patients with COPD. The drug generated global sales of 3.3 billion euros ($4.3 billion) in the second quarter of this year.
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