drugset / Trial / NCT01565902

Pharmacokinetics of BAF312 in Patients With Hepatic Impairment

NCT01565902

Phase 1 Completed 40 enrolled Novartis Pharmaceuticals
Non-randomizedParallel-groupOpen-labelOther

Summary

This study will investigate the pharmacokinetics of BAF312 in patients with mild, moderate and severe hepatic impairment compared to healthy control subjects.

Timeline

Start
2012-10
Primary completion
2014-03
Completion
2014-03

Drugs

EvaluationDrugModalityDoseRoute
Subject BAF312 Unknown 0.25 mg Oral

Indications

No indication recorded.