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
| Type | Name | Description |
|---|---|---|
| DRUG | Amlodipine-benazepril 10 mg-20 mg capsules | 1 x 10-20 mg |
| DRUG | Lotrel® 10 mg-20 mg capsule | 1 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.