drugset / Trial / NCT01136551

Comparative Bioavailability Study of an Immediate Release and Controlled Release Oral Formulations of Huperzine A

NCT01136551

RandomizedCrossoverOpen-labelTreatment

Summary

The purpose of this study is to develop oral controlled release formulation of Huperzine A that will provide optimal pharmacokinetic profile of the drug enhancing safety and compliance, as possible cure to neurodegenerative disorders.

Timeline

Start
2010-09
Primary completion
2011-01
Completion
2011-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Huperzine A Traditional medicine (herbal / TCM) 0.4 mg Oral

Indications

No indication recorded.