drugset / Trial / NCT02639221

A Phase I, Double Blind, Placebo Controlled, First in Human, Single and Multiple Ascending Oral Dose, Safety, Tolerability and Pharmacokinetic Study in Healthy Male and Female Subjects

NCT02639221

Phase 1 Completed 64 enrolled Prexton Therapeutics
RandomizedParallel-groupDouble-blind

Summary

The principal aim of this study is to obtain safety and tolerability data when PXT002331 is administered orally as single and multiple doses to healthy subjects.

Timeline

Start
2016-01
Primary completion
2016-08
Completion
2016-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Foliglurax Small molecule Oral

Indications