Bimekizumab is a humanized monoclonal antibody directed towards IL-17, which was approved for use in the EU on August 20, 2021, for the treatment of plaque psoriasis. It is the first IL-17 inhibitor to target both IL-17A and IL-17F. It has demonstrated superior efficacy as compared to another IL-17 inhibitor, secukinumab, as well as ustekinumab (an IL-12/23 inhibitor) and adalimumab (a TNF inhibitor) in the treatment of moderate-to-severe psoriasis, likely owing to its dual inhibition of both IL-17A and IL-17F. Bimekizumab was also granted FDA approval on October 18, 2023.
Bimekizumab is indicated for the treatment of moderate-to-severe plaque psoriasis in adults who are candidates for systemic therapy or phototherapy.
Pa0016 50662, Gilbert, Arizona, United States
Pa0016 40819, Sofia, Bulgaria
Pa0016 40012, Zlin, Czechia
Hs0005 50105, Saint Louis, Missouri, United States
Hs0005 50194, Omaha, Nebraska, United States
Hs0005 50140, Birmingham, Alabama, United States
Stay informed with timely notifications on clinical trials, regulatory changes, and research advancements related to this medication.