drugset / Trial / NCT05441904

Study to Assess the Safety, Tolerability, and Pharmacokinetics of PXL770 in Healthy Subjects.

NCT05441904 ↗

Phase 1 Completed 16 enrolled Poxel SA
NaSingle-groupOpen-labelTreatment

Summary

The study was planned in 2 parts: Parts A and B. In Part A, we tested 2 single doses of the study medicine in healthy volunteers: 500 mg and 750 mg. Part B was an optional part to test once-daily doses of the study medicine in healthy volunteers. We aimed to assess the safety, tolerability find out the side effects and blood levels of the PXL770.

Timeline

Start
2021-03-08
Primary completion
2021-03-29
Completion
2021-03-29

Drugs

EvaluationDrugModalityDoseRoute
Subject PXL770 Unknown 500 mg —
Subject PXL770 Unknown 750 mg —