Trials / Completed
CompletedNCT01735344
Bioequivalence Study of Lisinopril Tablets 40 mg Under Fed Condition
A Randomized, Balanced, Open Label, Two Treatment, Two Period, Two Sequence, Single Dose, Crossover, Bioequivalence Study of Lisinopril Tablets 40 mg With Zestril® (Lisinopril) 40 mg Tablets in Normal, Healthy, Adult, Male and Female Human Subjects Under Fed Conditions.
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 40 (actual)
- Sponsor
- IPCA Laboratories Ltd. · Industry
- Sex
- All
- Age
- 18 Years – 45 Years
- Healthy volunteers
- Accepted
Summary
This is a randomized, balanced, open Label, two-treatment, two-period, two-sequence, single dose, crossover pivotal study. The purpose of this study is to assess the bioequivalence between Test Product and the corresponding Reference Product under fed condition in normal, healthy, adult, male and female human subjects.
Detailed description
Objective of this pivotal study was to assess the bioequivalence between Test Product: Lisinopril Tablets 40 mg of Ipca Laboratories Limited, India and the corresponding Reference Product: Zestril® (Lisinopril) 40 mg Tablets of AstraZeneca Pharmaceuticals LP USA, under fed condition in normal, healthy, adult, male and female human subjects in a randomized crossover study. The study was conducted with 40 healthy adult subjects. In each study period, a single 40 mg dose of either test or reference was administered to the subjects as per the randomization schedule in each study period with about 240 mL of water at ambient temperature in sitting position. The duration of the clinical phase was approximately 18 days including washout period of 14 days between administrations of study drug in each study period.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Lisinopril Tablets 40 mg | 40 mg tablet once a day |
| DRUG | Lisinopril | 40 mg tablet once a day |
Timeline
- Start date
- 2012-06-01
- Primary completion
- 2012-08-01
- Completion
- 2012-08-01
- First posted
- 2012-11-28
- Last updated
- 2012-12-03
Locations
1 site across 1 country: India
Source: ClinicalTrials.gov record NCT01735344. Inclusion in this directory is not an endorsement.