Clinical Trials Directory

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

TypeNameDescription
DRUGVenlafaxine Hydrochloride150 mg Extended-Release Capsule
DRUGEffexor® XR150 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.

Venlafaxine Hydrochloride 150 mg Extended-Release Capsules Under Fasting Conditions (NCT01260896) · Clinical Trials Directory