Bimekizumab
IL17AF | |
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Clinical data | |
Trade names | Bimzelx |
Other names | UCB4940, bimekizumab-bkzx |
License data |
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Pregnancy category | |
Routes of administration | Subcutaneous |
ATC code | |
Legal status | |
Legal status | |
Identifiers | |
CAS Number | |
DrugBank | |
UNII | |
KEGG | |
Chemical and physical data | |
Formula | C6552H10132N1750O2029S42 |
Molar mass | 147229.87 g·mol−1 |
Bimekizumab, sold under the brand name Bimzelx, is a humanized anti-IL17A, anti-IL-17F, and anti-IL17AF
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).[6] Injection site reactions were also common, reported in 3% of subjects.[8]
Bimekizumab was approved for medical use in the European Union in August 2021,[6][9][10] and in the United States in October 2023.[11][12]
Medical uses
In the EU, bimekizumab is
History
Bimekizumab is being developed by Belgian pharmaceutical company UCB.[citation needed]
Society and culture
Names
Bimekizumab is the international nonproprietary name (INN).[13]
Research
Phase III trials have demonstrated that bimekizumab is superior to not only adalimumab[14] but also secukinumab[15] and ustekinumab[16] for the treatment of plaque psoriasis.
References
- ^ a b "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. Archived from the original on 3 April 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.
- ^ "Regulatory Decision Summary for Bimzelx". Drug and Health Products Portal. 23 February 2024. Retrieved 1 April 2024.
- ^ "Bimzelx- bimekizumab injection, solution". DailyMed. 20 October 2023. Retrieved 10 November 2023.
- ^ a b c d e f "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.
- PMID 31190730.
- ^ FDA Professional Drug Information
- ^ "Bimzelx Product information". Union Register of medicinal products. Archived from the original on 4 March 2023. 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.
- ^ Frellick M (18 October 2023). "FDA Approves Bimekizumab for Plaque Psoriasis in Adults". Medscape. Archived from the original on 28 October 2023. Retrieved 28 October 2023.
- ^ "Bimzelx Approved by the U.S. FDA for the Treatment of Adults with Moderate to Severe Plaque Psoriasis". UCB (Press release). 18 October 2023. Archived from the original on 28 October 2023. Retrieved 28 October 2023.
- hdl:10665/331112.
- S2CID 233372177.
- S2CID 233370455.
- S2CID 231809826.
Further reading
- Reis J, Vender R, Torres T (August 2019). "Bimekizumab: The First Dual Inhibitor of Interleukin (IL)-17A and IL-17F for the Treatment of Psoriatic Disease and Ankylosing Spondylitis". BioDrugs. 33 (4): 391–399. S2CID 174812750.