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Tofacitinib and azathioprine in alopecia areata

Efficacy and safety of Tofacitinib versus Azathioprine in severe alopecia areata, alopecia universalis and alopecia totalis.

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220904055876N1
Enrollment
60
Registered
2022-09-20
Start date
2022-10-04
Completion date
Unknown
Last updated
2022-11-21

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

Conditions

Alopecia Areata. Alopecia areata

Interventions

Patients in group A will receive tofacitinib at 5mg twice daily for 6 months and patients in group B will receive azathioprine in an oral dose of 1-2 mg/kg/day for 6 months.

Sponsors

Lady Reading Hospital Peshawar Pakistan
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients having Alopecia areata with =50% scalp hair loss, Alopecia totalis and Alopecia universalis. Patients must not have received any treatments for Alopecia areata within 2 months of enrollment and will not permitted to use any other treatment known to affect AA Stable or worsening disease for =6 months

Exclusion criteria

Exclusion criteria: Active malignancy or a history of malignancy Leukopenia, Anemia Hepatic or renal impairment Human immunodeficiency virus, Hepatitis B and C. Pregnant or nursing women

Design outcomes

Primary

MeasureTime frame
Severity of Alopecia Tool (SALT) score. Treatment will be considered efficacious if percent change in SALT score is > 50%. Timepoint: before intervention and 3 months and 6 months after intervention. Method of measurement: Severity of Alopecia Tool (SALT) score.

Countries

Pakistan

Contacts

Public ContactFarah Sagheer

Lady Reading Hospital Peshawar Pakistan

farah.sagheer@lrh.edu.pk+92 321 9049707

Outcome results

None listed

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