Phase 2 randomized, dose-ranging trial of CTP-543, a selective Janus Kinase inhibitor, in moderate-to-severe alopecia areata

被引:43
|
作者
King, Brett [1 ]
Mesinkovska, Natasha [2 ]
Mirmirani, Paradi [3 ,4 ,5 ]
Bruce, Suzanne [6 ]
Kempers, Steve [7 ]
Guttman-Yassky, Emma [8 ]
Roberts, Janet L. [9 ]
McMichael, Amy [10 ]
Colavincenzo, Maria [11 ]
Hamilton, Colleen [12 ]
Braman, Virginia [12 ]
Cassella, James, V [12 ]
机构
[1] Yale Univ, Sch Med, Dept Dermatol, 333 Cedar St,LMP 5040, New Haven, CT 06520 USA
[2] Univ Calif Irvine, Sch Med, Dept Dermatol, Irvine, CA 92717 USA
[3] Permanente Med Grp Inc, Dept Dermatol, Vallejo, CA USA
[4] Univ Calif San Francisco, Dept Dermatol, San Francisco, CA 94143 USA
[5] Case Western Reserve Univ, Dept Dermatol, Cleveland, OH 44106 USA
[6] Austin Inst Clin Res, Houston, TX USA
[7] Minnesota Clin Study Ctr, New Brighton, MN USA
[8] Icahn Sch Med Mt Sinai, New York, NY 10029 USA
[9] Northwest Dermatol Inst, Portland, OR USA
[10] Wake Forest Sch Med, Dept Dermatol, Winston Salem, NC 27101 USA
[11] Northwestern Univ, Feinberg Sch Med, Dept Dermatol, Chicago, IL 60611 USA
[12] Concert Pharmaceut Inc, Lexington, MA USA
关键词
AA; alopecia; alopecia areata; alopecia totalis; alopecia universalis; hair loss; JAK; JAK1; JAK2; JAK inhibitor; Janus kinase; ophiasis; patchy hair loss; SALT; PREVALENCE;
D O I
10.1016/j.jaad.2022.03.045
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Janus kinase (JAK) activation is suggested to have a pathological role in alopecia areata (AA). CTP-543, a deuterated compound that selectively inhibits JAK1 and JAK2, is being developed as an oral treatment for AA. Objective: To assess the safety and efficacy of a 24-week regimen of CTP-543 in patients with chronic, moderate-to-severe AA. Methods: In this phase 2, randomized, double-blind, placebo-controlled, sequential-design trial, patients were randomized to receive CTP-543 (4 mg, 8 mg, or 12 mg) or placebo every 12 hours for 24 weeks. Results: A dose-related increase was observed in the percentage of patients with >= 50% relative reduction in Severity of Alopecia Tool scores from baseline at week 24 (9% placebo, 21% 4 mg twice daily, 47% 8 mg twice daily, and 58% 12 mg twice daily), with statistical significance versus placebo (P<.001) observed for the 8-mg twice daily and 12-mg twice daily groups, with differences from placebo noted as early as 12 weeks after the initiation of treatment. Safety results were consistent with the known safety profiles of JAK inhibitors. Limitations: These initial findings are from a relatively small controlled trial, and additional studies are needed to fully characterize the safety and efficacy of CTP-543 in adult patients with AA. Conclusions: Patients treated with CTP-543 (8 or 12 mg, twice daily) had a significant reduction in the severity of AA.
引用
收藏
页码:306 / 313
页数:8
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