Viewing Study NCT01136551


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Study NCT ID: NCT01136551
Status: UNKNOWN
Last Update Posted: 2010-06-03
First Post: 2010-06-02
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Comparative Bioavailability Study of an Immediate Release and Controlled Release Oral Formulations of Huperzine A
Sponsor: Hadassah Medical Organization
Organization:

Study Overview

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.
Status: UNKNOWN
Status Verified Date: 2010-05
Last Known Status: NOT_YET_RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief 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.
Detailed Description: None

Study Oversight

Has Oversight DMC: True
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?:

Secondary ID Infos

Secondary ID Type Domain Link View
HUPA-HU-1 REGISTRY Haddasah University Hospital View