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NCT07559474
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
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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