NCT05522556|Unknown
Pre-approval Single-patient Expanded Access for Ritlecitinib (PF-06651600)
1 other identifier
B798
Study Type
expanded_access
Target
N/A
Locations
0 countries
Sites
N/A
Timeline
RegisteredAug 2022
Brief Summary
Provide pre-approval single patient Expanded Access (compassionate use) of Ritlecitinib for patients.
Trial Health
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 26, 2022
Completed5 days until next milestone
First Posted
Study publicly available on registry
August 31, 2022
CompletedLast Updated
November 18, 2025
Status Verified
November 1, 2025
First QC Date
August 26, 2022
Last Update Submit
November 17, 2025
Conditions
Keywords
Alopecia Areata (AA)AlopeciaPatchy AAAlopecia Universalis (AU)Alopecia Totalis (AT)OphiasisEyelash LossEyebrow LossHair Loss
Interventions
RitlecitinibDRUG
capsules
Eligibility Criteria
Age12 Years+
Sexall
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Must have ≥ 50% hair loss on scalp due to Alopecia Areata (AA) and be intolerant or have inadequate response to all commonly used AA therapies accessible in the country. Additional eligibility criteria may be required.
Contact the study team to discuss eligibility requirements. They can help determine if this study is right for you.
Sponsors & Collaborators
- Pfizerlead
MeSH Terms
Conditions
Alopecia AreataAlopeciaAlopecia universalis
Condition Hierarchy (Ancestors)
HypotrichosisHair DiseasesSkin DiseasesSkin and Connective Tissue DiseasesPathological Conditions, AnatomicalPathological Conditions, Signs and Symptoms
Central Study Contacts
Study Design
- Study Type
- expanded access
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 26, 2022
First Posted
August 31, 2022
Last Updated
November 18, 2025
Record last verified: 2025-11