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Sussex","BN2 5BE",{"type":127,"coordinates":2604},[2605,2606],-0.13947,50.82838,{"lat":2606,"lon":2605},{"facility":2609,"status":120,"city":2610,"state":2611,"zip":2612,"country":2591,"countryCode":2592,"cosmosGeoPoint":2613,"geoPoint":2617,"contacts":106},"Gloucestershire Royal Hospital \u002FID# 257953","Gloucester","Gloucestershire","GL1 3NN",{"type":127,"coordinates":2614},[2615,2616],-2.2431,51.86568,{"lat":2616,"lon":2615},{"facility":2619,"status":120,"city":2620,"state":2621,"zip":2622,"country":2591,"countryCode":2592,"cosmosGeoPoint":2623,"geoPoint":2627,"contacts":106},"Chelsea and Westminster Hospital \u002FID# 259128","London","Greater London","SW10 9NH",{"type":127,"coordinates":2624},[2625,2626],-0.12574,51.50853,{"lat":2626,"lon":2625},{"facility":2629,"status":120,"city":2630,"state":2631,"zip":2632,"country":2591,"countryCode":2592,"cosmosGeoPoint":2633,"geoPoint":2637,"contacts":106},"Oxford University Hospitals NHS Foundation Trust \u002FID# 257948","Oxford","Oxfordshire","OX3 9DU",{"type":127,"coordinates":2634},[2635,2636],-1.25596,51.75222,{"lat":2636,"lon":2635},{"facility":2639,"status":120,"city":2640,"state":106,"zip":2641,"country":2591,"countryCode":2592,"cosmosGeoPoint":2642,"geoPoint":2646,"contacts":106},"London North West University Healthcare NHS Trust \u002FID# 257914","Harrow","HA1 3UJ",{"type":127,"coordinates":2643},[2644,2645],-0.33208,51.57835,{"lat":2645,"lon":2644},{"facility":2648,"status":120,"city":2649,"state":106,"zip":2650,"country":2591,"countryCode":2592,"cosmosGeoPoint":2651,"geoPoint":2655,"contacts":106},"Northern Care Alliance NHS Group \u002FID# 257952","Salford","M6 8HD",{"type":127,"coordinates":2652},[2653,2654],-2.29042,53.48771,{"lat":2654,"lon":2653},{"type":2657,"investigatorFullName":106,"investigatorTitle":106,"investigatorAffiliation":106,"oldNameTitle":106,"oldOrganization":106},"SPONSOR","100054201","phase-3-a-study-to-evaluate-the-safety-and-effectiveness-of-upadacitinib-tablets-in-adult-and-adolescent-participants-with-severe-alopecia-areata-100054201",false,"NCT06012240","A Study to Evaluate the Safety and Effectiveness of Upadacitinib Tablets in Adult and Adolescent Participants With Severe Alopecia Areata","A Phase 3 Randomized, Placebo-controlled, Double-blind Program to Evaluate Efficacy and Safety of Upadacitinib in Adult and Adolescent Subjects With Severe Alopecia Areata","Up-AA","Inclusion Criteria:\n\n* Adult individuals must be \\\u003C 64 years old at Baseline Visit. Where permitted outside United States (US)\u002FEuropean Union (EU), adolescent individuals who are at least 12 years old at Screening may participate in Study 1 and Study 2. Adolescent individuals in the US who are at least 12 years old at Screening may participate in Study 4.\n* Diagnosis of severe alopecia areata (AA) with Severity of Alopecia Tool (SALT) score \\>= 50 scalp hair loss at Screening and Baseline.\n* Severe AA with no spontaneous scalp hair regrowth over the past 6 months.\n* Current episode of AA of less than 8 years.\n\nExclusion Criteria:\n\n* Current diagnosis of primarily diffuse type of AA.\n* Current diagnosis of other types of alopecia that would interfere with evaluation of AA, including but not limited to female pattern hair loss, male pattern hair loss (androgenetic alopecia) Stage III or greater based on Hamilton-Norwood classification, traction alopecia, lichen planopilaris (LPP), discoid lupus, frontal fibrosing alopecia (FFA), central centrifugal cicatricial alopecia (CCCA), folliculitis decalvans, trichotillomania, and telogen effluvium.\n* Diagnosis of other types of inflammatory scalp, eyebrow, or eyelash disorders that would interfere with evaluation of AA as determined by the investigator, including but not limited to seborrheic dermatitis, scalp psoriasis, atopic dermatitis (AD), and tinea capitis.","ALL","12 Years","63 Years",{"count":2670,"type":2671},1500,"ESTIMATED","INTERVENTIONAL",[2674],"PHASE3","Alopecia areata (AA) is a disease that happens when the immune system attacks hair follicles and causes hair loss. AA usually affects the head and face, but hair loss can happen on any part of the body. The purpose of this study is to assess how safe, effective, and tolerable upadacitinib is in adolescent and adult participants with severe AA.\n\nUpadacitinib is an approved drug being investigated for the treatment of AA. In Study 1 and Study 2 and Study 4 Period A, participants are placed in 1 of 3 groups, called treatment arms. Each group receives a different treatment. There is a 1 in 5 chance that participants will be assigned to placebo. In Study 1 and Study 2 and Study 4 Period B, participants originally randomized to upadacitinib dose group in Period A will continue their same treatment in Period B. Participants originally randomized to Placebo in Period A will either remain on placebo in Period B, or be randomized in 1 of 2 groups, based off of their Severity of Alopecia Tool (SALT) score. Participants who complete Study 1, Study 2 or Study 4, can join Study 3 and may be re-randomized to receive 1 of 2 doses of upadacitinib for up to 108 weeks. Around 1500 participants with severe AA will be enrolled in the study at approximately 280 sites worldwide.\n\nParticipants will receive oral tablets of either upadacitinib or placebo once daily for up to 160 weeks with the potential of being re-randomized into a different treatment group at Weeks 24 and 52. Participants will be followed up for up to 30 days after last study drug dose.\n\nThere may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at a hospital or clinic. The effect of the treatment will be checked by medical assessments, blood tests, checking for side effects and completing questionnaires.",[2677],"Alopecia Areata",[2677,97,101,102],"2026-07-10",{"date":2681,"type":2682},"2026-07-13","ACTUAL",{"date":2684,"type":2682},"2023-10-11",{"date":2686,"type":2671},"2030-04",{"name":5,"class":6},281]