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Study identifier: NCT07136467 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Non-Segmental Vitiligo (NSV) · Alopecia Areata · Hidradenitis Suppurativa  ·  Sponsor: AbbVie

PhaseN/A
Planned participants2795
Who can joinAll sexes, 12 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Beth Rycroft  ·  844-663-3742  ·  beth.rycroft@abbvie.com

Always discuss trial participation with your own doctor first.

Locations (116)

Hospital Britanico de Buenos Aires /ID# 278940Ciudad Autonoma de Buenos Aire, Buenos Aires, ArgentinaRecruiting
Buenos Aires Skin /ID# 277637Buenos Aires, ArgentinaRecruiting
Centro de Investigacion y Prevencion Cardiovascular (CIPREC) /ID# 277634Buenos Aires, ArgentinaRecruiting
Hospital Italiano de Buenos Aires /ID# 277636Buenos Aires, ArgentinaRecruiting
Instituto de Neumonología y Dermatología /ID# 277635Buenos Aires, ArgentinaRecruiting
Dermatology Research Institute - Blackfoot Trail /ID# 276548Calgary, Alberta, CanadaRecruiting
Rejuvenation Dermatology - Edmonton Downtown /ID# 276593Edmonton, Alberta, CanadaRecruiting
Alberta Dermatology Consultants /ID# 277187Edmonton, Alberta, CanadaRecruiting
Brunswick Dermatology Center /ID# 276546Fredericton, New Brunswick, CanadaRecruiting
Simcoderm Medical And Surgical Dermatology Centre /ID# 276838Barrie, Ontario, CanadaRecruiting
DermEffects /ID# 276594London, Ontario, CanadaRecruiting
Lynderm Research Inc /ID# 276595Markham, Ontario, CanadaRecruiting

+ 104 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07136467