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NCT00777972 · ClinicalTrials.gov registry record · NA

Bioequivalence Study of Fosinopril Sodium/ Hydrochlorothiazide 20/ 12.5 mg Tablets Under Fasting Conditions

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

Completed
Registry status
NA
Development phase
34
Enrollment target
1
Study location

NCT00777972: Completed NA study of Healthy, sponsored by Ranbaxy Laboratories Limited.

NCT00777972 is a NA study of Healthy that has completed, run by Ranbaxy Laboratories Limited. The registered enrollment target is 34 participants, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (95% 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

NCT00777972, a NA study of Healthy, has completed, sponsored by Ranbaxy Laboratories Limited.

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

Study Summary

The objective of this study was to compare the relative bioavailability of Fosinopril sodium and hydrochlorothiazide 20-12.5 mg tablets by Ranbaxy Laboratories Limited with that of Monopril ®.-HCT 20-12.5 mg tablets by Bristol-Meyers Squibb following a single oral dose (1 x 20-12.5 mg tablet) in healthy adult subjects under fasting conditions

Conditions Studied

Healthy

Interventions

  • DRUG Fosinopril sodium and hydrochlorothiazide 20-12.5 mg tablets

Study Locations (1)

Missouri

  • Gateway Medical Research Inc - Saint Charles

Trial Details

FieldValue
Enrollment Target 34 participants
Start Date 2003-03
Est. Completion 2003-04
Phase NA

Sponsor

Ranbaxy Laboratories Limited

44 total trials

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What the Registry Record Tells You About NCT00777972

The ClinicalTrials.gov registry entry for NCT00777972 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 34 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 (95% 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 Fosinopril sodium and hydrochlorothiazide 20-12.5 mg tablets is the first listed.

NCT00777972 reports 1 study location spanning 1 distinct geographic area - top geographies include Missouri.

Frequently Asked Questions

What is clinical trial NCT00777972 about?

NCT00777972 is a clinical study titled "Bioequivalence Study of Fosinopril Sodium/ Hydrochlorothiazide 20/ 12.5 mg Tablets Under Fasting Conditions". The objective of this study was to compare the relative bioavailability of Fosinopril sodium and hydrochlorothiazide 20-12.5 mg tablets by Ranbaxy Laboratories Limited with that of Monopril ®.-HCT 20-12.5 mg tablets by Bristol-Meyers Squibb following a single oral dose (1 x 20-12.5 mg tablet) in hea...

What is the current status of trial NCT00777972?

This trial is currently completed. It is a NA study. The enrollment target is 34 participants. The study started on 2003-03. Estimated completion is 2003-04.

What conditions does trial NCT00777972 study?

This clinical trial studies the following conditions: Healthy.

What interventions are being tested in trial NCT00777972?

The interventions under investigation include: Fosinopril sodium and hydrochlorothiazide 20-12.5 mg tablets (DRUG).

Who is sponsoring clinical trial NCT00777972?

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

Where is trial NCT00777972 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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Read our methodology - how this data is sourced, computed, and verified.
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.