The FDA's review of the BLA for bimekizumab for the treatment of psoriasis is continuing. A decision on the approval application has been delayed until the third quarter of this year. DermTwitter
by the end of June. No reason for the delay was provided in the company's press release.
Bimekizumab is a monoclonal antibody that inhibits interleukin -17A and IL-17F, two drivers of inflammation. The manufacturer, UCB, is seeking approval in the United States for the treatment of adults with moderate to severeThe biologic has been approved for the treatment of moderate to severe psoriasis in the European Union as well as in Canada, Australia, Japan, and Saudi Arabia. It is marketed as Bimzelx.
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