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Clinical Trial ● Currently Recruiting Phase III NCT06855498

Rollover Study for Participants Previously Enrolled in Clinical Trials of Povorcitinib

Rollover Study for Participants Previously Enrolled in Clinical Trials of Povorcitinib — Recruiting • Phase III • Respiratory / COPD / Asthma • NCT06855498.

📅 25 Mar 2026 ⏱ 2 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Phase III
NCT ID
NCT06855498
Sponsor
Incyte Corporation
Start
2025-02-28
ClinicaliQ Trial Snapshot
  • Rollover Study for Participants Previously Enrolled in Clinical Trials of Povorcitinib — Recruiting • Phase III • Respiratory / COPD / Asthma • NCT06855498.
  • Rollover study for participants from predetermined, Incyte-sponsored parent clinical trials of povorcitinib.
  • Sponsor: Incyte Corporation.

Verify eligibility, endpoints and current status on the original source registry before acting on this summary.

Use This Page For
  • Quick orientation before opening the registry record.
  • Checking recruitment status, phase and sponsor at a glance.
  • Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying

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

Eligibility Snapshot
  • : * Ability to comprehend and willingness to sign a written ICF for the study. * Completed the treatment period of a predetermined, Incyte-sponsored, povorcitinib parent study without safety or tolerability concerns, per investigator's assessment. * Received clinical benefit from treatment with study drug during the parent study, as determined by the investigator. * Demonstrated compliance, as assessed by the investigator, with the parent Protocol requirements. * Willingness to avoid pregnancy or fathering children as defined in the protocol. * Willingness and ability to comply with the study Protocol and procedures.

Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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