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NCT00778791 · ClinicalTrials.gov registry record · NA

Bioequivalence Study of Metformin HCl 750 mg XR Under Fasting Conditions

A NA study of Healthy, sponsored by Ranbaxy Laboratories Limited.

Completed
Registry status
NA
Development phase
60
Enrollment target
1
Study location

NCT00778791: Completed NA study of Healthy, sponsored by Ranbaxy Laboratories Limited.

NCT00778791 is a NA study of Healthy that has completed, run by Ranbaxy Laboratories Limited. The registered enrollment target is 60 participants, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (91% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00778791, a NA study of Healthy, has completed, sponsored by Ranbaxy Laboratories Limited.

COMPLETED
Registry status
NA
Development phase
60 participants
Enrollment target
1
Study location

Study Summary

The objective of this study is to compare the relative bioavailability of metformin HC1 750 mg extended-release tablets (Ranbaxy) with that of Glucophage® XR 750 mg tablets (Bristol Myers Squibb) in healthy, adult, subjects under fasting conditions.

Conditions Studied

Interventions

  • DRUG metformin HC1 750 mg extended-release tablets

Study Locations (1)

Missouri

  • Gateway medical research - Saint Charles

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2004-04
Est. Completion 2004-07
Phase NA

Sponsor

Ranbaxy Laboratories Limited

44 total trials

What the Registry Record Tells You About NCT00778791

The ClinicalTrials.gov registry entry for NCT00778791 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (91% lower). The listed sponsor is Ranbaxy Laboratories Limited, which has 44 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Healthy appearing as the primary indexed condition, and to 1 intervention - of which metformin HC1 750 mg extended-release tablets is the first listed.

NCT00778791 reports 1 study location spanning 1 distinct geographic area - top geographies include Missouri.

Frequently Asked Questions

What is clinical trial NCT00778791 about?

NCT00778791 is a clinical study titled "Bioequivalence Study of Metformin HCl 750 mg XR Under Fasting Conditions". The objective of this study is to compare the relative bioavailability of metformin HC1 750 mg extended-release tablets (Ranbaxy) with that of Glucophage® XR 750 mg tablets (Bristol Myers Squibb) in healthy, adult, subjects under fasting conditions.

What is the current status of trial NCT00778791?

This trial is currently completed. It is a NA study. The enrollment target is 60 participants. The study started on 2004-04. Estimated completion is 2004-07.

What conditions does trial NCT00778791 study?

This clinical trial studies the following conditions: Healthy.

What interventions are being tested in trial NCT00778791?

The interventions under investigation include: metformin HC1 750 mg extended-release tablets (DRUG).

Who is sponsoring clinical trial NCT00778791?

This trial is sponsored by Ranbaxy Laboratories Limited, which has 44 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00778791 being conducted?

This trial has 1 study location across Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.