drugset / Trial / NCT01027169

A Study to Assess the Effect of Hepatic Impairment on Safinamide Pharmacokinetics

NCT01027169

Phase 1 Completed 24 enrolled Newron Pharmaceuticals SPA
Non-randomizedParallel-groupOpen-labelBasic science

Summary

The primary purpose of this study is to investigate the pharmacokinetics (behavior of the compound in the body) of safinamide in patients with different degrees of hepatic (liver) impairment in comparison to matched subjects with normal hepatic function.

Timeline

Start
2009-04
Primary completion
2009-10
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Safinamide Small molecule 50 mg

Indications

No indication recorded.