Bimekizumab
Bimekizumab, sold under the brand name Bimzelx, is a humanized anti-IL17A, anti-IL-17F, and anti-IL17AF monoclonal antibody[4][5] that is used to treat plaque psoriasis, psoriatic arthritis, axial spondyloarthritis, and ankylosing spondylitis.[4]
Monoclonal antibody | |
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Type | Whole antibody |
Source | Humanized |
Target | IL17A, IL17F, IL17AF |
Clinical data | |
Trade names | Bimzelx |
License data | |
Pregnancy category | |
ATC code | |
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The most common side effects include upper respiratory tract infections (nose and throat infection) and oral candidiasis (thrush, a fungal infection in the mouth or throat).[4]
Bimekizumab was approved for medical use in the European Union in August 2021.[4][6][7]
Medical uses
In the EU, bimekizumab is indicated for the treatment of moderate to severe plaque psoriasis, active psoriatic arthritis, non-radiographic axial spondyloarthritis, and active ankylosing spondylitis.[4]
History
Bimekizumab is being developed by Belgian pharmaceutical company UCB.
Society and culture
Names
Bimekizumab is the international nonproprietary name (INN).[8]
Research
Phase III trials have demonstrated that bimekizumab is superior to not only adalimumab[9] but also secukinumab[10] and ustekinumab[11] for the treatment of plaque psoriasis.
References
- "Bimzelx APMDS". Therapeutic Goods Administration (TGA). 7 April 2022. Archived from the original on 24 April 2022. Retrieved 24 April 2022.
- "Updates to the Prescribing Medicines in Pregnancy database". Therapeutic Goods Administration (TGA). 21 December 2022. Retrieved 2 January 2023.
- "Bimzelx Product information". Health Canada. 25 April 2012. Archived from the original on 29 June 2022. Retrieved 29 June 2022.
- "Bimzelx EPAR". European Medicines Agency (EMA). 23 June 2021. Archived from the original on 25 August 2021. Retrieved 24 August 2021. Text was copied from this source which is © European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
- Lim SY, Oon HH (13 May 2019). "Systematic review of immunomodulatory therapies for hidradenitis suppurativa". Biologics. 13: 53–78. doi:10.2147/BTT.S199862. PMC 6526329. PMID 31190730.
- "Bimzelx Product information". Union Register of medicinal products. Retrieved 3 March 2023.
- "UCB Announces European Commission Approval of Bimzelx (bimekizumab) for the Treatment of Adults with Moderate to Severe Plaque Psoriasis". UCB (Press release). 24 August 2021. Archived from the original on 25 August 2021. Retrieved 24 August 2021.
- World Health Organization (2014). "International nonproprietary names for pharmaceutical substances (INN): recommended INN: list 72". WHO Drug Information. 28 (3). hdl:10665/331112.
- Warren RB, Blauvelt A, Bagel J, Papp KA, Yamauchi P, Armstrong A, et al. (July 2021). "Bimekizumab versus Adalimumab in Plaque Psoriasis". The New England Journal of Medicine. 385 (2): 130–141. doi:10.1056/NEJMoa2102388. PMID 33891379. S2CID 233372177.
- Reich K, Warren RB, Lebwohl M, Gooderham M, Strober B, Langley RG, et al. (July 2021). "Bimekizumab versus Secukinumab in Plaque Psoriasis". The New England Journal of Medicine. 385 (2): 142–152. doi:10.1056/NEJMoa2102383. PMID 33891380. S2CID 233370455.
- Reich K, Papp KA, Blauvelt A, Langley RG, Armstrong A, Warren RB, et al. (February 2021). "Bimekizumab versus ustekinumab for the treatment of moderate to severe plaque psoriasis (BE VIVID): efficacy and safety from a 52-week, multicentre, double-blind, active comparator and placebo controlled phase 3 trial". Lancet. 397 (10273): 487–498. doi:10.1016/S0140-6736(21)00125-2. PMID 33549193. S2CID 231809826.