CorEvitas International Adolescent Alopecia Areata (AA) Drug Safety and Effectiveness Registry
Key facts
- Where
- Waltham, United StatesSee the site
Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 12 and 17 years old?
Source: NCT06562270, who can take part
Where in United States
- CorEvitas, LLCWaltham, United StatesContact: Cathy CheneyTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorTrial details
- Who runs it
- CorEvitas
- Trial code
- NCT06562270
- Record updated
- 17 August 2026
- Original description
Prospective observational registry focusing on an adolescent cohort diagnosed with severe alopecia areata,receiving routine care from dermatology providers. Visit schedules for patients will be determined by the provider in accordance with routine clinical care, and any prescriptions provided to patients will adhere to product availability and local prescribing guidelines/regulations in the country where the participating registry site is located.Read full original descriptionShow less
Prospective observational registry focusing on an adolescent cohort diagnosed with severe alopecia areata,receiving routine care from dermatology providers. Visit schedules for patients will be determined by the provider in accordance with routine clinical care, and any prescriptions provided to patients will adhere to product availability and local prescribing guidelines/regulations in the country where the participating registry site is located.
Inclusion: To be eligible to participate in this registry, an individual must meet all the following criteria:; Has ever been diagnosed with severe AA by a dermatologist or a qualified healthcare provider; Is 12-17 years of age at the time of enrollment; Is willing to provide consent/assent for participation in the registry.
Exclusion: Is participating or planning to participate in a blinded clinical trial for any investigational medication; An individual who meets any of the following criteria will be excluded from participation in the registry:; Is unwilling or unable to provide standing height measurements.