BMS’ Plaque Psoriasis Drug Deucravacitinib Among Six Hopefuls Awaiting EMA Verdict

A novel TYK2 inhibitor and a drug to treat an ultra-rare genetic disorder are among products up for a marketing authorization opinion this week from the European Medicines Agency’s human medicines committee, the CHMP.

Concept of EMA European Medicines Agency. Drugs evaluation and quality control.
Companies Could Soon Learn If Their Products Have Won The EMA’s Backing • Source: Shutterstock

Bristol Myers Squibb’s deucravacitinib and Ipsen’s palovarotene are among the latest drugs for which the European Medicines Agency is due to adopt an opinion this week on whether or not they should be granted EU-wide marketing approval.

Deucravacitinib is for treating plaque psoriasis, while palovarotene is for the ultra-rare genetic disorder fibrodysplasia ossificans progressiva (FOP), which causes soft tissues to transform permanently into bone

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