Clinical Trials Directory

Trials / Completed

CompletedNCT01149733

Tamsulosin Hydrochloride 0.4 mg Capsules Under Fed Conditions

A Single-Dose, Comparative Bioavailability Study of Two Formulations of Tamsulosin Hydrochloride 0.4 mg Capsules Under Fed Conditions

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
32 (actual)
Sponsor
Teva Pharmaceuticals USA · Industry
Sex
Male
Age
18 Years
Healthy volunteers
Accepted

Summary

The objective of this study is to evaluate the comparative bioavailability between tamsulosin hydrochloride 0.4 mg capsules (Manufactured by Teva Pharmaceutical Industries Ltd.; distributed by Teva Pharmaceuticals USA) and Flomax® (tamsulosin hydrochloride)0.4 mg capsules (Manufactured by Yamanouchi Pharmaceutical Co., Japan; distributed by Boehringer Ingelheim Pharmaceutical Inc. USA), after a single-dose in healthy subjects under fed conditions.

Conditions

Interventions

TypeNameDescription
DRUGTamsulosinTest 0.4 mg Capsule
DRUGTamsulosinReference Listed 0.4 Capsule

Timeline

Start date
2004-11-01
Primary completion
2004-11-01
Completion
2004-11-01
First posted
2010-06-23
Last updated
2024-08-20
Results posted
2010-09-13

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01149733. Inclusion in this directory is not an endorsement.