A Study to Assess the Safety and Pharmacokinetics of INCB123667 When Administered Orally to Adult Participants With Moderate or Severe Hepatic Impairment

This study will be conducted to assess the safety and pharmacokinetics of INCB123667 when administered orally to adult participants with moderate or severe hepatic impairment.

Trial Details

NCT ID
NCT07559474
Phase
PHASE1
Sponsor
Incyte Corporation
Status
RECRUITING
Cancer Type
Liver Cancer
Interventions
  • INCB123667
Locations (sample)
  • Chandler, Arizona, United States|33.30616,-111.84125
  • Orlando, Florida, United States|28.53834,-81.37924
  • San Antonio, Texas, United States|29.42412,-98.49363
  • San Antonio, Texas, United States|29.42412,-98.49363

Key Eligibility Criteria

  • Ability to comprehend and willingness to sign a written ICF for the study.
  • Aged 18 to 80 years, inclusive, at the time of signing the ICF.
  • Moderate or severe hepatic impairment based on CP score.
  • Medical findings consistent with the degree of hepatic dysfunction, determined by medical history, physical examination, vital sign measurements, 1…

For full eligibility, visit ClinicalTrials.gov.

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