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Recruiting Observational

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

NCT06573593 · tracked via the Priya Life Science China tracker
Phase
Observational
Started
2024-07-29
Last updated
2024-08-27

Condition(s) studied

Alopecia AreataJanus Kinase Inhibitors

Investigational drug(s) / intervention(s)

Tofacitinib →Baricitinib →Ruxolitinib →Upadacitinib →Abrocitinib →Ritlecitinib →

Tofacitinib: In the real-world settings, patients with AA treated with tofacitinib.

Baricitinib: In the real-world settings, patients with AA treated with Baricitinib.

Ruxolitinib: In the real-world settings, patients with AA treated with Ruxolitinib.

Upadacitinib: In the real-world settings, patients with AA treated with Upadacitinib.

Abrocitinib: In the real-world settings, patients with AA treated with Abrocitinib.

Ritlecitinib: In the real-world settings, patients with AA treated with Ritlecitinib.

Study summary

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

Sex
ALL
Min age
2 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * 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 Exclusion Criteria: * 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 * Patients are participating in other clinical trials

Primary outcome measure(s)

  • Mean SALT — at week 24
    Reduction of Severity of Alopecia Tool (SALT) score compared with baseline
  • SALT50 — at week 24
    Percentage of patient with more than 50% improvement in SALT score
  • SALT75 — at week 24
    Percentage of patient with more than 70% improvement in SALT score

Trial sites (1)

FacilityCityRegionStatus
Second Affiliated Hospital, School of Medicine, Zhejiang University, China Hangzhou Zhejiang Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06573593 on ClinicalTrials.gov ↗ ← All trials in China