Treatment of hidradenitis with JAK inhibitors
A technology for inhibitors and hidradenitis suppurativa, applied in medical preparations containing active ingredients, pharmaceutical formulas, drug combinations, etc., can solve unsatisfied, good and other problems, and achieve the effect of improving HiSCR scores
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Embodiment 1
[0198] Hidradenitis Suppuratitis Clinical Response (HiSCR)
[0199] This study is ongoing to provide data on efficacy, safety, tolerability and pharmacokinetics of the therapeutic agents being tested in the oral treatment of moderate to severe HS. The maximum duration of the study will be approximately 26 weeks. This includes a screening period of up to 6 weeks, a dosing period of 16 weeks, and a follow-up period of 4 weeks. The study will enroll approximately 192 participants in total (expected to provide approximately 156 completers). After the screening period, participants who met eligibility criteria at the baseline visit will be randomly assigned to receive 1 of 6 treatments. One oral dose level of each therapeutic agent will be investigated: [(1S)-2,2-difluorocyclopropyl][(1R,5S)-3-{2-[(1-methyl-1H-pyrazole -4-yl)amino]pyrimidin-4-yl}-3,8-diazabicyclo[3.2.1]oct-8-yl]methanone (45 mg QD) and (1r,3r)-3- (cyanomethyl)-3-(4-(6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]py...
Embodiment 2
[0202] Lesion count
[0203] Number of inflammatory and non-inflammatory nodules, abscesses, draining and non-draining fistulas, and hypertrophic scars, and physical location (right / left axilla, right / left under breast, breast room, right / left buttock, right / left groin Femoral folds, perianal, perineal, others) will be assessed according to standards in the art.
Embodiment 3
[0205] Abscess count
[0206] The number of abscesses (variable, with or without drainage, tenderness or pain) will be counted at each site as defined above.
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