drugset / Trial / NCT03212313

Study to Investigate the Influence of Hepatic Insufficiency on the Pharmacokinetics of Tozadenant

NCT03212313

Phase 1 Terminated 20 enrolled Biotie Therapies Inc. Acorda Therapeutics · collab
Non-randomizedSequentialOpen-labelBasic science

Summary

This is a two-part, open label, single-dose study that will evaluate the PK of tozadenant in subjects with different degrees of hepatic impairment to the PK of a single-dose of tozadenant in healthy subjects.

Timeline

Start
2017-06-30
Primary completion
2017-12-31
Completion
2017-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Tozadenant Small molecule 120 mg

Indications

No indication recorded.