Clinical Trials Directory

Trials / Completed

CompletedNCT00835367

Amlodipine-Benazepril 10mg-20mg Capsules in Healthy Subjects Under Fed Conditions

Randomized, 2-way, Crossover, Bioequivalence Study of Amlodipine-Benazepril 10mg-20mg Capsules and Lotrel® Administered as 1 x 10 Mg-20 mg Capsule in Healthy Subjects Under Fed Conditions.

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

Summary

The objective of this study is to compare the rate and extent of absorption if amlodipine-benzazepril 10 mg-20 mg capsules (test) versus Lotrel® (reference),administered as 1 x 10 mg- 20 mg capsule under fed conditions.

Detailed description

Criteria for Evaluation: FDA Bioequivalence Criteria Statistical Methods: FDA bioequivalence statistical methods

Conditions

Interventions

TypeNameDescription
DRUGAmlodipine-benazepril 10 mg-20 mg capsules1 x 10-20 mg
DRUGLotrel® 10 mg-20 mg capsule1 x 10-20 mg

Timeline

Start date
2004-03-01
Primary completion
2004-03-01
Completion
2004-03-01
First posted
2009-02-03
Last updated
2024-08-21
Results posted
2009-08-18

Locations

2 sites across 1 country: Canada

Source: ClinicalTrials.gov record NCT00835367. Inclusion in this directory is not an endorsement.

Amlodipine-Benazepril 10mg-20mg Capsules in Healthy Subjects Under Fed Conditions (NCT00835367) · Clinical Trials Directory