drugset / Trial / NCT00490945

Safety and Efficacy of VEC-162 on Circadian Rhythm in Healthy Adult Volunteers

NCT00490945

Phase 2 Completed 45 enrolled Vanda Pharmaceuticals
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to assess the safety and efficacy of VEC-162 compared to matching placebo on circadian phase shift and sleep parameters.

Timeline

Start
2004-07
Primary completion
2005-03
Completion
2005-03

Drugs

EvaluationDrugModalityDoseRoute
Subject tasimelteon Small molecule 10 mg
Subject tasimelteon Small molecule 20 mg
Subject tasimelteon Small molecule 50 mg
Subject tasimelteon Small molecule 100 mg