Clinical Trials Directory

Trials / Completed

CompletedNCT01160068

Bioequivalence Study of Metformin Hydrochloride Tablets 1000 mg Tablets of Dr. Reddy's Laboratories Limited Under Fed Condition

A Randomized, Two-treatment, Two-period, Two-sequence, Single Dose, Crossover Bioequivalence Study of Metformin Hydrochloride 1000 mg Tablets (Dr. Reddy's Laboratories Ltd., Generics, India) to be Compared With Glucophage® (Metformin Hydrochloride) 1000 mg Tablets (Bristol-Myers Squibb, USA) in 48 + (2 Standby) Healthy, Adult, Human Subjects Under Fed Conditions

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

Summary

To compare the single dose bioavailability of Metformin Hydrochloride 1000 mg tablets (Dr. Reddy's Laboratories Ltd., Generics, India) with Glucophage (Metformin Hydrochloride) 1000 mg tablets (Bristol-Myers Squibb, USA) in 48 + (2 standby) healthy, adult, human subjects under fed conditions. To monitor adverse events and to ensure the safety of subjects.

Detailed description

Open label, balanced, randomized, two-treatment, two-period, two-sequence, single dose,crossover bioequivalence study with at least 07 days of washout period between each drug administration under fed conditions.

Conditions

Interventions

TypeNameDescription
DRUGMetforminMetformin Tablets 1000 mg
DRUGGlucophageGlucophage 1000 mg tablets of Bristol-Myers Squibb

Timeline

Start date
2005-02-01
Primary completion
2005-05-01
Completion
2005-05-01
First posted
2010-07-12
Last updated
2010-07-13

Locations

1 site across 1 country: India

Source: ClinicalTrials.gov record NCT01160068. Inclusion in this directory is not an endorsement.