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Trials / Completed

CompletedNCT00729729

Pharmacokinetic Study for PCA Derivate Formulations

Phase 4, Three Way Cross-over, Pharmacokinetic Study for PCA Derivate Formulations in Healthy Subjects

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
30 (estimated)
Sponsor
Hadassah Medical Organization · Academic / Other
Sex
Male
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

A comparative bioavailability study of PCA slow release versus immediate release formulations, after a single dose to fasting healthy subjects.

Conditions

Interventions

TypeNameDescription
DRUGPCAPlacebo tablet, once
DRUGPCAPO, 700mg, once
DRUGPCAPO, 1000mg, once

Timeline

Start date
2008-07-01
Primary completion
2009-02-01
Completion
2009-12-01
First posted
2008-08-07
Last updated
2012-08-28

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT00729729. Inclusion in this directory is not an endorsement.

Pharmacokinetic Study for PCA Derivate Formulations (NCT00729729) · Clinical Trials Directory