EMA approve UCB’s treatment Cimzia for psoriasis
European Medicines Agency has approved a label extension for UCB’s Cimzia allowing it to be used for treating adults with moderate-to-severe plaque psoriasis who are candidates for systemic therapy.
The approval makes Cimzia, the first Fc-free, PEGylated anti-TNF treatment option for use in moderate-to-severe plaque psoriasis “and marks the entry of UCB into immuno-dermatology, where significant unmet need currently exists,” the firm noted.
The CIMPASI-1 and -2 and CIMPACT trials confirmed the efficacy and safety of the drug in this setting.
In all three trials, the drug showed “statistically significant improvements for all primary and co-primary endpoints compared to placebo at all tested doses”, and the clinical benefit was maintained through to week 48, according to the firm.
In the CIMPACT trial, the response rate for patients who achieved a PASI 75 after 12 weeks’ treatment was 67% for those receiving Cimzia 400mg every two weeks and 61% for those getting Cimzia 200mg every two weeks, compared to just 5% for patients in the placebo group.
At week 16, response rates for patients who achieved a PASI 75 were 75% and 68%, respectively, versus 4% for those taking a placebo.
“Despite available treatments, patients with moderate-to-severe plaque psoriasis can still experience poor control of symptoms, which can significantly impact their quality of life.
“[The] approval provides patients and their healthcare professionals with a biologic option with 10 years of clinical experience in multiple inflammatory disease indications that may offer durable disease control for psoriasis patients in Europe,” said Professor Richard Warren, consultant dermatologist, Salford Royal NHS Foundation Trust.
Psoriasis affects around 3% of the world’s population, approximately 125 million people worldwide.
In Europe, Cimzia is already approved as a treatment for rheumatoid arthritis, active psoriatic arthritis and axial spondyloarthritis (axSpA).