Tofacitinib for the Treatment of Alopecia Areata and Its Variants
Part of paid clinical trials in Stanford, California.
- Sponsor
- Stanford University
- Study ID
- NCT02312882
- Status
- Completed
Conditions
- Alopecia Areata
- Alopecia Totalis
- Alopecia Universalis
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Tofacitinib — DRUGTofacitinib 5 mg tablet taken by mouth twice a day.
Study Details
The purpose of this study is to investigate the ability of tofacitinib citrate, a Janus kinase inhibitor, to generate hair regrowth in patients with moderate to severe alopecia areata and its variants.
Key Dates
- Start date
- Dec 31, 2014
- Status verified
- Oct 2017
- Primary completion
- Aug 31, 2015
- Completion
- Aug 31, 2015
Study Design
- Enrollment
- 40 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: TofacitinibParticipants will receive tofacitinib for 3 months.
Primary Outcome Measure
Percent Change in Severity of Alopecia Tool (SALT) Score [ Time Frame: 0 and 3 months ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Stanford University | Stanford | California | 94305 | - |
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