Recently, At the American Academy of Dermatology's annual meeting, UCB presented new data showing that results from two phase 3 trials testing the drug candidate in hidradenitis suppurativa held up through 48 weeks. In new 48-week data, more than 75% of patients maintained a 50% reduction in skin abscesses and inflammatory nodules in the studies. Around 55% of participants experienced a 75% reduction after 48 weeks of treatment. The longer-term data give UCB confidence to pursue a potential second indication for its drug. The company aims to begin submitting applications in moderate to severe hidradenitis suppurativa by this year’s third quarter, UCB said in a statement.
Hidradenitis suppurativa (HS) is a chronic inflammatory skin disease mainly affecting areas rich in apocrine glands. Its frequency is estimated to be 0.5-4% of the general population, affecting women more often. Pathogenesis of HS is still not clearly defined. It seems to be a combination of genetic factors with alterations in the skin microbiome. Furthermore, at tissue (i.e. skin) as well as at serum level, several inflammatory cytokines are upregulated. The most important of the latter are tumor necrosis factor (TNF), interleukin (IL)-1, IL-17, and IL-23.
Search the drug intelligence database:Synapse, a total of 54 drugs and 228 clinical trials were found for the treatment of Hidradenitis suppurativa. For this indication, the top three research and development organizations are Novartis, Pfizer and AbbVie, the major R&D targets are focused on TNF-α、IL-17A and JAK1. The top three types of drug development for this indication are Monoclonal antibody, Biosimilar, and Small molecule drug.
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来源: SYNAPSE
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