NCT07559474RecruitingPhase 1
A Study to Assess the Safety and Pharmacokinetics of INCB123667 When Administered Orally to Adult Participants With Moderate or Severe Hepatic Impairment
A Phase 1, Open-Label Study to Assess the Safety and Pharmacokinetics of INCB123667 When Administered Orally to Adult Participants With Moderate or Severe Hepatic Impairment
Source: ClinicalTrials.gov · Last updated 16 Jun 2026
Brief summary (registry, in English)
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.
- Status (registry)
- Recruiting
- Phase (registry)
- Phase 1
- Study type
- Interventional
- Enrollment
- 16 (estimated)
- First submitted
- 24 Apr 2026
- Start date
- 27 May 2026
- Primary completion date
- 13 Apr 2027
- Lead sponsor
- Incyte Corporation
- NCT number
- NCT07559474
What you commit to
- Study type: Interventional · Phase 1
- Planned participants: 16
- From 27 May 2026 to the primary completion date, 13 Apr 2027
- 4 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Participants who have a current, functioning organ transplant or are on the national transplant list and expected to receive a transplant within 3 months.
- Tobacco or nicotine-containing product use of \> 10 cigarettes per day within 1 month before screening.
- Participants who had a change in disease status within 30 days before screening, as documented by the participant's medical history, that is deemed clinically significant by the investigator.
- Participants who have a history of paracentesis within 2 months prior to check-in.
- Participants who required new medication or an increase in dose for hepatic encephalopathy within 3 months prior to check-in.
- Participants who had esophageal banding within 3 months prior to check-in or required any other treatment for gastrointestinal bleeding within 6 months prior to check-in.
- Other protocol-defined Inclusion/Exclusion Criteria may apply.
Lab values
- Participants who have a history of unstable diabetes mellitus (as evidenced by hemoglobin A1c ≥ 10.0%). Medications for treatment of diabetes mellitus must be reviewed and approved by the investigator and medical monitor. Participants who have a portal systemic shunt. Up to 3 participants with transjugular intrahepatic portosystemic shunt may be included.
Who the study is looking for
- 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, 12-lead ECGs, and clinical laboratory determinations at screening or check-in (as applicable). Participants with abnormal findings considered not clinically significant by the medical monitor or investigator are eligible.
- Body mass index of 18.0 to 43.0 kg/m2 (inclusive).
- Willingness to avoid pregnancy or fathering children.
Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers
Sites (4)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Arizona Clinical Trials - the Institute For Liver Health Coordinator of this site? Confirm its status | Chandler | United States | Recruiting |
| Orlando Clinical Research Center Coordinator of this site? Confirm its status | Orlando | United States | Recruiting |
| Texas Liver Institute - American Research Corporation Coordinator of this site? Confirm its status | San Antonio | United States | Recruiting |
| Pinnacle Clinical Research Coordinator of this site? Confirm its status | San Antonio | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.