A Real World Study to Globally Assess Disease Burden in Adolescent and Adult Participants With Alopecia Areata, Vitiligo, or Hidradenitis Suppurativa

Recruiting Observational Study
Non-Segmental Vitiligo (NSV) Alopecia Areata Hidradenitis Suppurativa
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
12 and older
Sex
Any
Study type
Observational
Participants needed
2,795 (estimated)
Sponsor
AbbVie · Industry
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About This Trial

This study is to assess the burden of disease in adolescent and adult participants with moderate or severe alopecia areata (AA), non-segmental vitiligo (NSV), or moderate to severe hidradenitis suppurativa (HS) in a large global real-world participant population.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Participants with Physician-confirmed diagnosis of non-segmental vitiligo (NSV), moderate to severe Alopecia Areata (AA), or moderate to severe hidradenitis suppurativa (HS) * Participants Ability to understand study questionnaires, with caregiver support as required for adole…
Contacts

Beth Rycroft

844-663-3742

beth.rycroft@abbvie.com

CONTACT