Trials / Completed
CompletedNCT01712100
Crossover Bioequivalence Study of Irbesartan 300 mg Tablets Under Fed Conditions
A Single Dose, 2-Period, 2-Treatment, 2-Way Crossover Bioequivalency Study of Irbesartan Tablets Under Fed Conditions
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 34 (actual)
- Sponsor
- Roxane Laboratories · Industry
- Sex
- All
- Age
- 18 Years – 45 Years
- Healthy volunteers
- Accepted
Summary
The objective of this study was to prove the bioequivalence of Roxane Laboratories' Irbesartan 300 mg Tablets under fed conditions.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Irbesartan | |
| DRUG | Avapro |
Timeline
- Start date
- 2007-08-01
- Primary completion
- 2007-08-01
- Completion
- 2007-08-01
- First posted
- 2012-10-23
- Last updated
- 2018-01-23
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01712100. Inclusion in this directory is not an endorsement.