Phase
Condition
Primary Biliary Cholangitis
Treatment
varegacestat
Clinical Study ID
Ages 18-84 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria (Healthy Participants):
Healthy, adult, male or female (of nonchildbearing potential only), 18 to 84 years of age, inclusive, at the screening visit. Participant will be matched by age (± 10 years) and sex to a participant with hepatic impairment (HI). Each healthy participant may be matched to more than 1 participant with HI, but cannot be matched to more than 1 participant within the same HI group.
Medically healthy with no clinically significant medical history, physical examination, clinical laboratory profiles, vital signs, and ECGs as deemed by the PI or designee
Inclusion Criteria (Hepatic Impairment):
Healthy, apart from HI, adult male or female (of nonchildbearing potential only), 18 to 84 years of age, inclusive, at the screening visit.
Considered to have HI (of any etiology) that has been clinically stable (no acute episodes of illness due to deterioration in hepatic function) for at least 1 month prior to dosing per the PI and Sponsor and is likely to remain stable throughout the study. To be classified as having hepatic impairment with known medical history of liver disease (with or without a known history of alcohol abuse).
Has a score on the Child-Pugh scale at screening visit and confirmed at check-in as follows:
Mild: ≥5 and ≤6 [Category A]; or
Moderate: ≥7 and ≤9 [Category B]; or
Severe: ≥10 and ≤15 [Category C].
- Medically healthy, apart from HI, with no clinically significant medical history, physical examination, clinical laboratory profiles, vital signs, and ECGs as deemed by the PI or designee
Exclusion Criteria (Healthy Volunteers):
Is mentally or legally incapacitated or has significant emotional problems at the time of the screening visit or expected during the conduct of the study.
History or presence of clinically significant medical or psychiatric condition or disease in the opinion of the PI or designee.
History of any illness that, in the opinion of the PI or designee, might confound the results of the study or pose an additional risk to the participant by their participation in the study.
Exclusion Criteria (Hepatic Impairment):
Participants must not be enrolled in the study, if they meet any of the following criteria:
Is mentally or legally incapacitated or has significant emotional problems at the time of the screening visit or expected during the conduct of the study.
History or presence of clinically significant medical (except for HI) or psychiatric condition or disease in the opinion of the PI or designee.
History of any illness that, in the opinion of the PI or designee, might confound the results of the study or pose an additional risk to the participant by their participation in the study.
Study Design
Study Description
Connect with a study center
Orlando Clinical Research Center
Orlando, Florida 32809
United StatesActive - Recruiting
The Texas Liver Institute
San Antonio, Texas 78215
United StatesActive - Recruiting
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