Sanofi: extension of marketing authorization for Dupixent in the EU
The marketing authorization for this chronic inflammatory disease covers adults and adolescents aged 12 and over, weighing at least 40 kg and inadequately controlled by, intolerant of or not recommended for conventional drugs.
Approximately 60% of patients aged 12 and over treated with Dupixent 300 mg once weekly in a pivotal trial showed histological remission, as well as a significant improvement in their ability to swallow, compared to placebo.
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