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A real-world study of the efficacy of Tofacitinib in the treatment of patients with alopecia areata

A single-arm,open,multicenter and real-world study of the efficacy and safety of Tofacitinib in the treatment of patients with alopecia areata

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400081744
Enrollment
Unknown
Registered
2024-03-11
Start date
2024-03-15
Completion date
Unknown
Last updated
2024-03-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

alopecia areata

Interventions

treatment group:Tofacitinib 11mg qd

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1) Subjects are between the ages of 18-55 years old, including both males and females; 2) Meet the diagnostic criteria for pemphigus vulgaris; 3) Those who did not receive topical or systemic treatment for the first time before the baseline visit or who have received treatment but it is ineffective, and who are able to comply with the medication prescribed by the doctor and have regular follow-up visits; 4) Blood and urine routine, common evaluation indexes of liver function (alanine aminotransferase, glutamine aminotransferase, alkaline phosphatase and gamma-glutamyl transpeptide, etc.) and common evaluation indexes of renal function (blood creatinine, endogenous creatinine clearance, urea nitrogen, etc.) are within the normal range; 5) No other autoimmune diseases were found; 6) Signed informed consent and picture authorization

Exclusion criteria

Exclusion criteria: 1) Pregnant and lactating women, and men with recent plans to have children; 2) Those with other concurrent alopecia lesions (e.g., androgenetic alopecia, tinea capitis, hair-pulling fetish, etc.); 3) Those who use other drugs that affect the observation of the efficacy of this study before the baseline visit (e.g. use of CYP3A4 inhibitors, etc.); 4) Severe hepatic or renal insufficiency; 5) Active tuberculosis, hepatitis B, syphilis, immunodeficiency virus (HIV) infected subjects, etc.

Design outcomes

Primary

MeasureTime frame
SALT;

Secondary

MeasureTime frame
Dermatoscope Pictures;

Countries

China

Contacts

Public ContactYuping Ran

West China Hospital, Sichuan University

ranyuping@vip.sina.com+86 189 8060 1697

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026