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Study identifier: NCT06855498 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Rollover Study for Participants Previously Enrolled in Clinical Trials of Povorcitinib

Condition: Hidradenitis Suppurativa (HS)  ·  Sponsor: Incyte Corporation

PhasePhase 3
Planned participants600
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Rollover study for participants from predetermined, Incyte-sponsored parent clinical trials of povorcitinib.

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

Talk to the study team

Incyte Corporation Call Center (US)  ·  1.855.463.3463  ·  medinfo@incyte.com

Incyte Corporation Call Center (ex-US)  ·  +800 00027423  ·  eumedinfo@incyte.com

Always discuss trial participation with your own doctor first.

Locations (318)

Investigative Site US106Birmingham, Alabama, United StatesNot Yet Recruiting
Investigative Site US086Birmingham, Alabama, United StatesRecruiting
Investigative Site US098Montgomery, Alabama, United StatesNot Yet Recruiting
Investigative Site US004Phoenix, Arizona, United StatesRecruiting
Investigative Site US047Scottsdale, Arizona, United StatesWithdrawn
Investigative Site US115Tucson, Arizona, United StatesNot Yet Recruiting
Investigative Site US076Fountain Valley, California, United StatesRecruiting
Investigative Site US077Fremont, California, United StatesRecruiting
Investigative Site US071Huntington Beach, California, United StatesRecruiting
Investigative Site US097Irvine, California, United StatesNot Yet Recruiting
Investigative Site US020Laguna Niguel, California, United StatesRecruiting
Investigative Site US036Los Angeles, California, United StatesRecruiting

+ 306 more locations — full list on the registry record.

Follow this study

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This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06855498