drugset / Trial / NCT01271387

Pharmacokinetics of Tasimelteon in Subjects With Mild or Moderate Hepatic Impairment

NCT01271387

Phase 1 Completed 29 enrolled Vanda Pharmaceuticals
Non-randomizedParallel-groupOpen-labelBasic science

Summary

The purpose of this research study is to understand whether there is any difference in the amount of tasimelteon (including its breakdown products) in the blood in individuals with mild or moderate liver disease compared to individuals who have normal liver function.

Timeline

Start
2011-01
Primary completion
2011-08
Completion
2011-08

Drugs

EvaluationDrugModalityDoseRoute
Subject tasimelteon Small molecule 20 mg Oral

Indications

No indication recorded.