Efficacy and Safety of JAK Inhibitors in Patients With AA: RWE Study

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age2-80
SponsorSecond Affiliated Hospital, School of Medicine, Zhejiang University

About this trial

The introduction of Janus Kinase inhibitors (JAKi) seems to revolutionize the field of alopecia areata (AA) therapeutics. However, the ideal JAKi is not yet settled and the real-world data are still missing. To provide evidence about effectiveness and safety of different JAKi including tofacitinib, baricitinib, ritlecitinib,abrocitinib, upadacitinib and ifidancitinib in real-world settings and describe baseline disease characteristics and patients profiles that are considered good candidates for JAKi in the daily practice. Furthermore, we intended to investigate the efficacy and safety of JAK Inhibitors in patients With AA, as well as to provide clinical evidence for the clinicians and patients when they formulate individualized treatment plans.

Eligibility criteria

Qualifiers

Patients with alopecia areata between 2 to 18 years old

Patients diagnosed with alopecia areata according to AA guideline

AA Patients treated with JAKi including tofacitinib, baricitinib, ritlecitinib,abrocitinib, upadacitinib and ifidancitinib for more than 3 months

Disqualifiers

Patients had previously received hair implants

Other alopecia

Other diseases may induce alopecia including psoriasis, lichen planus, et al.

Unable to estimate SALT score at baseline or at follow-up

Trial design

Treatments tested in this trial

  • Tofacitinib
  • Baricitinib
  • Ruxolitinib
  • Upadacitinib
  • Abrocitinib
  • Ritlecitinib

Treatment groups

150 Participants
are divided into 6 treatment groups

6

Treatment groups

See each treatment group below.