Clinical Trials Directory

Trials / Completed

CompletedNCT00650312

Fasting Study of Metformin Hydrochloride ER Tablets 500 mg and Glucophage® XR Tablets 500 mg

Single-Dose Fasting In Vivo Bioequivalence Study of Metformin Hydrochloride ER Tablets (500 mg; Mylan) and Glucophage® XR Tablets (500 mg; Bristol-Myers Squibb) in Healthy Volunteers

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
50 (actual)
Sponsor
Mylan Pharmaceuticals Inc · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The objective of this study is to investigate the bioequivalence of Mylan metformin hydrochloride ER tablets to Glucophage® XR tablets following a single, oral 500 mg (1 x 500 mg) dose administration under fasting conditions.

Conditions

Interventions

TypeNameDescription
DRUGMetformin Hydrochloride ER Tablets 500 mg500mg, single dose fasting
DRUGGlucophage® XR Tablets 500 mg500mg, single dose fasting

Timeline

Start date
2002-10-01
Primary completion
2002-10-01
Completion
2002-11-01
First posted
2008-04-01
Last updated
2024-04-24

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00650312. Inclusion in this directory is not an endorsement.