Overview

A Study to Evaluate the Pharmacokinetic Profiles of Single 14 mg Teriflunomide Tablet in Healthy Chinese Volunteers

Status:
Completed
Trial end date:
2014-07-01
Target enrollment:
Participant gender:
Summary
Primary Objective: To assess the pharmacokinetic (PK) parameters of teriflunomide after a single oral dose of 14 mg administration in Chinese healthy subjects Secondary Objective: To assess the safety and tolerability after a single oral dose of 14 mg teriflunomide in Chinese healthy subjects
Phase:
Phase 1
Details
Lead Sponsor:
Sanofi
Treatments:
Cholestyramine Resin
Teriflunomide