Trials / Completed
CompletedNCT00602849
Bioequivalency Study of Sertraline Under Fasting Conditions
A Single Dose, Two-Period, Two-Treatment, Two-Way Crossover Bioequivalency Study of Sertraline Tablets 100 mg Under Fasting Conditions
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 38 (actual)
- Sponsor
- Roxane Laboratories · Industry
- Sex
- All
- Age
- 18 Years – 45 Years
- Healthy volunteers
- Accepted
Summary
The objective of this study was the bioequivalence of a Roxane Laboratories' Sertraline Tablets, 100 mg, to Zoloft® Tablets, 100 mg (Pfizer) under fasting conditions using a single-dose, 2-treatment, 2-period, crossover design.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Sertraline |
Timeline
- Start date
- 2003-06-01
- Primary completion
- 2003-07-01
- Completion
- 2003-07-01
- First posted
- 2008-01-28
- Last updated
- 2018-01-23
Locations
1 site across 1 country: Canada
Source: ClinicalTrials.gov record NCT00602849. Inclusion in this directory is not an endorsement.