Clinical Trials Directory

Trials / Completed

CompletedNCT02322619

Bio-equivalency Study of Moxifloxacin Tablets, 400 mg Under Fasting Conditions

An Open Label, Balanced, Randomized, Two-treatment, Two-period, Two-sequence, Single Dose, Crossover, Oral Bioequivalence Study of Moxifloxacin Tablets, 400 mg of Dr. Reddy's Laboratories Limited, Comparing With Avelox® Tablets 400 mg of Bayer Healthcare Pharmaceuticals Inc. in Healthy, Adult Human Subjects Under Fasting Conditions

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

Summary

An open label, balanced, randomized, two-treatment, two-period, two-sequence, single dose, crossover, oral bioequivalence study in human subjects under fasting conditions.

Detailed description

An open label, balanced, randomized, two-treatment, two-period, two-sequence, single dose, crossover, oral bioequivalence study of moxifloxacin tablets 400 mg of Dr. Reddy's Laboratories Limited, comparing with Avelox ® Tablets 400 mg of Bayer Healthcare Pharmaceuticals Inc. in healthy, adult, human subjects under fasting conditions.

Conditions

Interventions

TypeNameDescription
DRUGMoxifloxacin Tablets 400 mgMoxifloxacin Tablets 400 mg of Dr. Reddy's Laboratories Limited

Timeline

Start date
2012-11-01
Primary completion
2012-12-01
Completion
2012-12-01
First posted
2014-12-23
Last updated
2014-12-23

Source: ClinicalTrials.gov record NCT02322619. Inclusion in this directory is not an endorsement.