Trials / Completed
CompletedNCT00861549
Bioavailability, Pharmacokinetics and Safety Evaluation of Phencynonate Hydrochloride in Healthy Volunteers
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 32 (actual)
- Sponsor
- PhytoHealth Corporation · Industry
- Sex
- Male
- Age
- 18 Years – 40 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to evaluate the bioavailability of two formulations (Taiwan and China mainland) of phencynonate hydrochloride tablets and to generate pharmacokinetic and safety profiles of phencynonate hydrochloride in healthy volunteers.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Phencynonate hydrochloride | 2mg/tablet |
Timeline
- Start date
- 2008-08-01
- Primary completion
- 2010-01-01
- Completion
- 2010-01-01
- First posted
- 2009-03-13
- Last updated
- 2025-06-04
Locations
1 site across 1 country: Taiwan
Source: ClinicalTrials.gov record NCT00861549. Inclusion in this directory is not an endorsement.