July 2024 batch of EMA/CHMP positive opinions
The European Medicines Agency’s (EMA) human medicines committee (CHMP) recommended seven novel medicines for approval at its July 2024 meeting.
The CHMP recommended granting a marketing authorization for Denmark-based LEO Pharma’s Anzupgo (delgocitinib), a medicine intended for the treatment of moderate to severe chronic hand eczema in adults for whom topical corticosteroids are inadequate or inappropriate.
The committee recommended granting a conditional marketing authorization for Iqirvo (elafibranor), from French drugmaker Ipsen (Euronext: IPN), for the treatment of primary biliary cholangitis, a chronic and progressive autoimmune disease that can cause liver damage.
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