Clinical Trials Directory

Trials / Completed

CompletedNCT01167933

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

A Randomized, Two-treatment, Two-period, Two-sequence, Single Dose, Crossover Bioequivalence Study of Simvastatin 80 mg Tablets of Dr. Reddy's to be Compared With Zocor® 80 mg Tablets of Merck & Co. Inc., USA in Healthy Adult Subjects Under Fed Conditions

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
44 (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 the single dose bioavailability of Simvastatin 80 mg tablets with Zocor® 80 mg tablets of MercK \& Co. Inc, USA in healthy subjects under fed conditions * monitor adverse events and to ensure the safety of subjects.

Detailed description

A randomized, two-treatment, two-period, two-sequence, single dose, crossover bioequivalence study of Simvastatin 80 mg tablets of Dr. Reddy's Laboratories Limited to be compared with Zocor® 80 mg tablets of Merck \& Co. Inc., USA in healthy, adult, human subjects under fed conditions.

Conditions

Interventions

TypeNameDescription
DRUGSimvastatinSimvastatin 80 mg tablets Dr. Reddy's Laboratories Ltd

Timeline

Start date
2005-01-01
Primary completion
2005-04-01
Completion
2005-04-01
First posted
2010-07-22
Last updated
2010-08-09

Source: ClinicalTrials.gov record NCT01167933. Inclusion in this directory is not an endorsement.