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Clinical Trial Summary

A two part, fixed-sequence, open-label crossover study to evaluate potential CYP1A2-mediated drug-drug interactions of ABX464 in healthy subjects using caffeine and fluvoxamine as probe drugs


Clinical Trial Description

This is a Phase 1, 2 part, fixed-sequence open-label, crossover study to evaluate the potential CYP1A2-mediated drug-drug interactions (DDI), safety, and tolerability of ABX464 combined with a known CYP1A2 substrate (caffeine) and a known CYP1A2 inhibitor (fluvoxamine). Sixty (60) healthy adult male and female subjects 18 to 55 years of age are planned to participate in the study. Separate cohorts of subjects will be enrolled for Part A (24 subjects) and Part B (36 subjects). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05121714
Study type Interventional
Source Abivax S.A.
Contact
Status Completed
Phase Phase 1
Start date December 17, 2020
Completion date May 18, 2021

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