Clinical Trials Directory

Trials / Completed

CompletedNCT01645423

Bioequivalence Study of Atorvastatin Calcium Tablets, 80 mg of Dr. Reddy's Under Fed Conditions

An Open Label, Balanced, Randomized, Two-treatment, Two-period, Two-way Crossover Oral BE Study of Atorvastatin Ca 80 mg Tablets of Dr. Reddy's and Lipitor 80 mg Tablets of Pfizer in Healthy Adult, Human Subjects Under Fed Conditions

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
77 (actual)
Sponsor
Dr. Reddy's Laboratories Limited · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to compare and evaluate the single-dose oral bioavailability and to monitor the safety of subjects.

Detailed description

An open label, balanced, randomized, two-treatment, two-period, two-way crossover oral bioequivalence' study of Atorvastatin Calcium 80 mg Tablets of Dr. Reddy's and Lipitor 80 mg Tablets of Pfizer Ireland Pharmaceuticals in healthy adult, human subjects under fed conditions.

Conditions

Interventions

TypeNameDescription
DRUGAtorvastatin Calcium Tablets, 80 mgAtorvastatin Calcium Tablets, 80 of Dr. Reddy's Laboratories Limited

Timeline

Start date
2009-08-01
Primary completion
2009-09-01
Completion
2009-09-01
First posted
2012-07-20
Last updated
2012-07-20

Locations

1 site across 1 country: India

Source: ClinicalTrials.gov record NCT01645423. Inclusion in this directory is not an endorsement.

Bioequivalence Study of Atorvastatin Calcium Tablets, 80 mg of Dr. Reddy's Under Fed Conditions (NCT01645423) · Clinical Trials Directory