Clinical Trials Directory

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

TypeNameDescription
DRUGLisinopril Tablets 40 mg40 mg tablet once a day
DRUGLisinopril40 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.