Trials / Completed
CompletedNCT01260896
Venlafaxine Hydrochloride 150 mg Extended-Release Capsules Under Fasting Conditions
Randomized, 2-way Crossover, Bioequivalence Study of Venlafaxine Hydrochloride 150 mg Extended-Release Capsules and Effexor® XR 150 mg Extended-Release Capsules Administered as 1 x 150 mg Extended-Release Capsule in Healthy Subjects Under Fasting Conditions.
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 24 (actual)
- Sponsor
- Teva Pharmaceuticals USA · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
The objective of this study was to compare the rate and extent of absorption of venlafaxine hydrochloride 150 mg extended-release capsules (test) versus Effexor® XR (reference) administered as 1 x 150 mg extended-release capsule under fasting conditions.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Venlafaxine Hydrochloride | 150 mg Extended-Release Capsule |
| DRUG | Effexor® XR | 150 mg Extended-Release Capsule |
Timeline
- Start date
- 2002-09-01
- Primary completion
- 2002-10-01
- Completion
- 2002-10-01
- First posted
- 2010-12-15
- Last updated
- 2011-02-21
- Results posted
- 2011-02-21
Locations
1 site across 1 country: Canada
Source: ClinicalTrials.gov record NCT01260896. Inclusion in this directory is not an endorsement.