Condition: Chronic Hepaititis B Infections · Sponsor: Aligos Therapeutics
This Phase 1 non-randomized, open-label, single-dose hepatic impairment study consists of 2 cohorts, conducted in 16 subjects, 8 subjects with moderate hepatic impairment (Cohort 1) and 8 subjects without hepatic impairment (Cohort 2), matched for age, body weight and, to the extent possible, for sex. The effect of hepatic impairment on the plasma pharmacokinetics of ALG-001075 will be assessed in subjects who have received single oral doses of pevifoscorvir sodium (ALG-000184).
This description comes directly from the study's public registry record.
Jen Rito · (800) 466-6059 · info@aligos.com
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| Orlando Clinical Research Center | Orlando, Florida, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07342868