Brussels, Belgium – 24th January 2022 – 07:00 – UCB, a global biopharmaceutical company, today announced that the Japanese Ministry of Health, Labor and Welfare (MHLW) has granted marketing authorization for BIMZELX® (bimekizumab) for the treatment of plaque psoriasis, generalized pustular psoriasis and psoriatic erythroderma in patients who are not sufficiently responding to existing treatments. Bimekizumab is the first approved psoriasis treatment in Japan that is designed to selectively and directly inhibit two key cytokines driving inflammatory processes – interleukin 17F (IL-17F) and interleukin 17A (IL-17A).
This announcement marks the third approval for bimekizumab worldwide, following marketing authorization in countries of the European Union/European Economic Area and Great Britain in August 2021 for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy.1,2
“The approval of BIMZELX® in Japan is an important milestone that reinforces UCB’s commitment to the dermatology community and to advancing standards of care in psoriasis,” said Emmanuel Caeymaex, Executive Vice President, Immunology Solutions and Head of US, UCB. “At UCB, our ambition is to transform the lives of people living with severe diseases. We are incredibly proud to bring a new psoriasis treatment option to healthcare professionals and patients in Japan to help support more patients in reaching their treatment goals.”
Psoriasis is a common, chronic inflammatory disease with primary involvement of the skin.3 There are several types of psoriasis, though plaque psoriasis is the most common, comprising between 58 percent and 97 percent of all cases.4 Plaque psoriasis is characterized by dry, red plaques, usually covered with silvery or white scales.4 Generalized pustular psoriasis is less common, affecting between 1.1 percent and 12 percent of all cases, and characterized by coalescing pustules, filled with non-infectious pus.4 Psoriatic erythroderma is the most serious type of psoriasis characterized by fiery redness and exfoliation of most of the body surface, affecting between 0.4 percent and 7 percent of all cases.4
The approval in Japan is supported by the positive results from the Phase 3/3b clinical studies, BE READY, BE VIVID, BE SURE and BE RADIANT which evaluated the efficacy and safety of bimekizumab compared with placebo, ustekinumab, adalimumab and secukinumab in adults with moderate to severe plaque psoriasis, as well as results from the open-label extension study BE BRIGHT.5,6,7,8,9 Bimekizumab demonstrated superior levels of skin clearance* compared to placebo, ustekinumab, adalimumab and secukinumab, and was generally well-tolerated.5,6,7,8,9 Full findings from the BE READY and BE VIVID studies are published in The Lancet, and the results from the BE SURE and BE RADIANT studies are published in The New England Journal of Medicine.5,6,7,8
UCB is committed to bringing bimekizumab to patients worldwide. Bimekizumab is currently under review by the U.S. Food and Drug Administration (FDA) for the treatment of moderate to severe plaque psoriasis in adults. Regulatory reviews are also underway in Australia, Canada and Switzerland.
*Bimekizumab was evaluated in Phase 3/3b studies versus placebo (co-primary endpoint; BE READY and BE VIVID), versus adalimumab (co-primary endpoint; BE SURE), versus ustekinumab (ranked secondary endpoint; BE VIVID) and versus secukinumab (primary endpoint; BE RADIANT).5,6,7,8
About BIMZELX® (bimekizumab)
Bimekizumab is a humanized monoclonal IgG1 antibody that is designed to selectively and directly inhibit both interleukin 17A (IL-17A) and interleukin 17F (IL-17F), two key cytokines driving inflammatory processes.10
About BIMZELX® ▼ in the EU/EEA*
In the EU, BIMZELX® is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy.1
*EU/EEA means European Union/European Economic Area
BIMZELX® ▼(bimekizumab) EU/EEA Important Safety Information in Psoriasis
The most frequently reported adverse reactions with bimekizumab were upper respiratory tract infections (14.5%) (most frequently nasopharyngitis) and oral candidiasis (7.3%). Common adverse reactions (≥1/100 to <1/10) were oral candidiasis, tinea infections, ear infections, herpes simplex infections, oropharyngeal candidiasis, gastroenteritis, folliculitis, headache, dermatitis and eczema, acne, injection site reactions, fatigue. Elderly may be more likely to experience certain adverse reactions such as oral candidiasis, dermatitis and eczema when using bimekizumab.
Bimekizumab is contraindicated in patients with hypersensitivity to the active substance or any of the excipients and in patients with clinically important active infections (e.g. active tuberculosis).
Bimekizumab may increase the risk of infections. Treatment with bimekizumab must not be administered in patients with any clinically important active infection. Patients treated with bimekizumab should be instructed to seek medical advice if signs or symptoms suggestive of an infection occur. Prior to initiating treatment with bimekizumab, patients should be evaluated for tuberculosis (TB) infection. Bimekizumab should not be given in patients with active TB and patients receiving bimekizumab should be monitored for signs and symptoms of active TB.
Cases of new or exacerbations of inflammatory bowel disease have been reported with bimekizumab.
Bimekizumab is not recommended in patients with inflammatory bowel disease. If a patient develops signs and symptoms of inflammatory bowel disease or experiences an exacerbation of pre-existing inflammatory bowel disease, bimekizumab should be discontinued and appropriate medical management should be initiated. Serious hypersensitivity reactions including anaphylactic reactions have been observed with IL-17 inhibitors. If a serious hypersensitivity reaction occurs, administration of bimekizumab should be discontinued immediately and appropriate therapy initiated.
Live vaccines should not be given in patients treated with bimekizumab.
Please consult the summary of product characteristics in relation to other side effects, full safety and prescribing information.