Study to Evaluate the Pharmacokinetics (PK) of E7090 (Herein Referred to as Tasurgratinib) and Its Metabolite in Participants With Mild and Moderate Hepatic Impairment Compared to Healthy Participants
Recruiting now · Phase 1
Conditions studied: Hepatic Impairment
In brief
The primary purpose of the study is to evaluate the effects of mild and moderate hepatic impairment on PK of tasurgratinib after a single dose administration.
Key facts
- Study ID
- NCT04271488
- Run by
- Eisai Co., Ltd.
- People needed
- 18
- Starts
- 2020-02-27
- Expected to finish
- 2026-11-30
- Last updated by the study team
- 2026-01-23
Who can join
Age: 20 and older, up to 79. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Body mass index (BMI) between 18 to 40 kilogram per square meter (kg/m\^2).
- For Cohorts A and B: stable hepatic impairment conforming to Child-Pugh classification A and B.
- For Cohort C: healthy participants matched to participants with hepatic impairment with regard to age (+/-10 years), body weight (+/-20 percent [%]), race and gender, and as determined by no clinically significant deviation from normal in medical history, physical examination, electrocardiogram (ECG), and clinical laboratory determinations.
You may not qualify if…
- Key Exclusion for all Participants:
- Following ocular disorders
- Current evidence of Grade 2 or higher corneal disorder
- Current evidence of active macular disorder (example, Age-related macular degeneration, central serous chorioretinal disease)
- Known to be human immunodeficiency virus (HIV) positive at Screening.
- A prolonged QT/QTc interval ([QT interval using Fridericia's formula] QTcF greater than (>) 480 millisecond [ms]) demonstrated on ECG.
- Additional Exclusion Criteria for Hepatically Impaired Participants (Cohorts A and B)
- In addition to the Exclusion Criteria above for all participants, other standard exclusion criteria for participants with hepatic impairment will be used. These include:
- Any significant acute medical illness (such as new conditions or exacerbation of pre-existing conditions) within 8 weeks of dosing.
- Presence of severe ascites, edema, or uncontrolled hepatic encephalopathy
- The participant's standard therapy/concomitant medication for diseases related to hepatic disease has not remained stable/unchanged for at least two weeks before dosing of study drug.
- Additional Exclusion Criteria for Healthy participants (Cohort C)
- In addition to the Exclusion Criteria for all participants, other standard exclusion criteria for healthy participants in Phase 1 studies will be used. These include:
- Syphilis as demonstrated by positive serology at Screening.
- Any abnormal finding based on physical examination, assessment of vital signs, ECG, or laboratory test results that requires treatment or clinical follow up based on investigators opinion.
Where it is running
- Eisai Trial Site #7 — Kyoto, Japan (enrolling)
- Eisai Trial Site #6 — Hakata, Fukuoka, Japan (enrolling)
- Eisai Trial Site #2 — Yuhu, Oita Prefecture, Japan (enrolling)
- Eisai Trial Site #3 — Bukyo-ku, Tokyo, Japan (enrolling)
- Eisai Trial Site #1 — Mintato-ku, Tokyo, Japan (enrolling)
- Eisai Trial Site #8 — Shinjuku-ku, Tokyo, Japan (enrolling)
- Eisai Trial Site #5 — Kofu, Yamanashi, Japan (enrolling)
- Eisai Trial Site #4 — Kurume, Fukuoka, Japan
Full record on ClinicalTrials.gov
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