Clin2
NCT06855498Possibly a fitRecruiting

Rollover study for patients who took povorcitinib before

Hidradenitis Suppurativa (HS)

Treatments studied

Part of Infections, Skin clinical trials.

This study is for people who have already taken the study drug povorcitinib in a previous trial and found it helpful. It lets you continue receiving the treatment and allows doctors to keep tracking its long-term safety and effects.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 3
Enrollment
600 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You must have finished treatment in a previous Incyte-sponsored study of povorcitinib without major safety issues.
  • You must have had a good response to povorcitinib in that earlier study, as decided by your doctor.
  • You must be willing to follow the study rules and avoid pregnancy or fathering children as outlined in the protocol.
  • You cannot have been permanently stopped from taking the study drug in the earlier trial.
  • You cannot have taken certain other immune-modulating drugs or live vaccines within 28 days before starting this study, or plan to take a live vaccine during the study.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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