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
| Type | Name | Description |
|---|---|---|
| DRUG | Tamsulosin | Test 0.4 mg Capsule |
| DRUG | Tamsulosin | Reference 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.