Clinical Trials Directory

Trials / Completed

CompletedNCT01161940

Bioequivalence Study of Nizatidine Capsules 300 mg of Dr.Reddy's Laboratories Limited Under Fasting Conditions

A Two-way Crossover Experimental Evaluation of Relative Bioavailabilities of Two Formulations of Nizatidine 300 mg Capsules in Healthy Human Subjects Under Fasting Conditions

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
26 (actual)
Sponsor
Dr. Reddy's Laboratories Limited · Industry
Sex
Male
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

This is a bioequivalence study of nizatidine Capsules 300 mg of Dr.Reddy's Laboratories Limited under fasting conditions

Detailed description

Open label, balanced, randomized, two-treatment, two-period, two sequence, single dose, crossover, comparative oral bioavailability study in healthy, adult, male human subjects under fasting conditions.

Conditions

Interventions

TypeNameDescription
DRUGNizatidineNizatidine Capsules 300 mg of Dr.Reddy's Laboratories Limited
DRUGAxidAxid 300 mg Capsules of Reliant Pharmaceuticals, US

Timeline

Start date
2004-07-01
Primary completion
2004-09-01
Completion
2004-09-01
First posted
2010-07-14
Last updated
2010-07-14

Source: ClinicalTrials.gov record NCT01161940. Inclusion in this directory is not an endorsement.