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

Healthy Clinical Trial

Official title:
An Open-label, Three-period, Crossover Study in Healthy Volunteers to Evaluate the Relative Bioavailability of Two Different Release Rate Controlled Release Formulations of Huperzine A (0.4mg)Compared to the Equivalent Dose of an Immediate Release Formulation.

Clinical Trial 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.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Bio-equivalence Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01136551
Study type Interventional
Source Hadassah Medical Organization
Contact Gregory Burshtein, MA
Phone 97226758665/4
Email bursht@gmail.com
Status Not yet recruiting
Phase N/A
Start date September 2010
Completion date April 2011
View Details
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