drugset / Trial / NCT07251153

Pharmacokinetic Comparison of Vonafexor Acid and Its Lysine Salt and Evaluation of Potential Drug-Drug Interactions

NCT07251153 ↗

Phase 1 Recruiting 40 enrolled Enyo Pharma
RandomizedCrossoverOpen-labelTreatment

Summary

The purpose of this study is to define and compare the pharmacokinetic (PK) and pharmacodynamic (PD) profile of EYP651 at two dose levels and compare it with Vonafexor Acid PK and PD profile, the Part A. In addition, Part B of the trial will assess the Drug-Drug Interactions (DDI) potential with the high dose of EYP651.

Timeline

Start
2025-10-28
Primary completion
2025-12-18
Completion
2026-10-28

Drugs

EvaluationDrugModalityDoseRoute
Subject EYP651 Unknown — —
Subject Vonafexor Acid Unknown — —

Indications

No indication recorded.