drugset / Trial / NCT02055300

Safety, Tolerability and Pharmacokinetics Study of LY03005

NCT02055300

Phase 1 Completed 88 enrolled Luye Pharma Group Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the safety and tolerability of escalating single oral doses of LY03005 in healthy subjects and to characterize the pharmacokinetics (PK) of escalating single oral doses of LY03005.

Timeline

Start
2014-02
Primary completion
2014-08
Completion
2014-08

Drugs

EvaluationDrugModalityDoseRoute
Comparator Desvenlafaxine Other / unclassified 50 mg
Subject Toludesvenlafaxine Small molecule 20 mg Oral
Subject Toludesvenlafaxine Small molecule 40 mg Oral
Subject Toludesvenlafaxine Small molecule 80 mg Oral
Subject Toludesvenlafaxine Small molecule 120 mg Oral
Subject Toludesvenlafaxine Small molecule 160 mg Oral
Subject Toludesvenlafaxine Small molecule 200 mg Oral