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A Study of 2 Doses of Ritlecitinib in People 12 Years of Age and Older With Alopecia Areata

← catalyst calendar

NCT06873945 · readout in 578 d

Sponsored by Pfizer (industry) · PFE — their whole pipeline →.

Phase
Phase 3
Status
Recruiting
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
1,330estimated
Sites
147
Countries
Canada, China, Czechia +8

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2025-04-01actualWhen the study began enrolling
Primary completion2028-03-19estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2028-03-19estimatedThe whole study's end, after follow-up
First posted2025-03-13actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-13actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Alopecia Areata

Interventions

  • Drug: Ritlecitinib 100 mg — also filed as PF-06651600, Litfulo
  • Drug: Ritlecitinib 50 mg — also filed as PF-06651600, Litfulo
  • Drug: Placebo - 100 mg
  • Drug: Placebo - 50 mg

Primary outcomes

what the primary-completion date above is the date OF
Part 1: Percentage of participants with absolute Severity of Alopecia Tool (SALT) score less than or equal to 20
measured Week 24
Part 2: Percentage of participants with TEAEs, SAEs, and AEs leading to discontinuation
measured Baseline to Follow-up visit (Week 52)
Part 2: Percentage of participants with clinically significant laboratory abnormalities
measured Baseline to Follow-up visit (Week 52)

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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