drugset / Trial / NCT01136551
Comparative Bioavailability Study of an Immediate Release and Controlled Release Oral Formulations of Huperzine A
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Huperzine A | Traditional medicine (herbal / TCM) | 0.4 mg | Oral |
Indications
No indication recorded.