Hepatitis B, Chronic Clinical Trial
Official title:
Study of the Drug Interaction of EYP001a With Entecavir in Healthy Subjects
This is a Phase 1, single-center, open-label, three subsequent dosing periods study to evaluate the drug-drug-interaction (DDI), pharmaco-kinetics (PK) and pharmacodynamics (PD), safety, and tolerability of a single dose of EYP100a combined with ETV in healthy men and women dosed in the morning under fasted conditions.
This is a Phase 1, single-center, open-label, three consecutive dosing periods study to
evaluate the drug-drug interaction, PK, safety, tolerability and PD of a single dose of
EYP100a combined with ETV in healthy men and women. Sixteen (16) adult male and female
healthy participants 18 to 60 years of age inclusive are planned to participate in the study.
Women of childbearing potential will be eligible to participate if she is non pregnant or non
lactating and willing to use adequate contraception.
All participants in the study will be monitored for safety after administration of the last
dose of investigational product and with a follow up visit. The DDI, PK, PD, safety and
tolerability of EYP001a and ETV will be assessed based on plasma-concentration profiles of
EYP001a and ETV, FXR related PD markers and the types and frequency of treatment-emergent
adverse events (TEAEs) reported, concomitant medication usage, and changes from baseline in
physical examination (PE), vital signs, electrocardiogram (ECG), and standard clinical
laboratory tests.
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