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NCT01149473 · ClinicalTrials.gov registry record · Phase 1

Losartan Potassium/Hydrochlorothiazide 100/25 mg Tablets in Healthy Subjects Under Non-Fasting Conditions

A Phase 1 study, sponsored by Teva Pharmaceuticals USA.

Completed
Registry status
Phase 1
Development phase
80
Enrollment target

NCT01149473: Completed Phase 1 study, sponsored by Teva Pharmaceuticals USA.

NCT01149473 is a Phase 1 study that has completed, run by Teva Pharmaceuticals USA. The registered enrollment target is 80 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01149473, a Phase 1 study, has completed, sponsored by Teva Pharmaceuticals USA.

COMPLETED
Registry status
Phase 1
Development phase
80 participants
Enrollment target

Study Summary

The objective of this study is to compare the relative bioavailability of Losartan potassium/Hydrochlorothiazide 100/25 mg tablets (manufactured by Teva Pharmaceutical Industries, Ltd. and distributed by Teva Pharmaceuticals USA) with that of Hyzaar® 100/25 mg tablets (Merck) in healthy, adult, non-smoking subjects under non-fasting conditions.

Interventions

  • DRUG Losartan potassium/Hydrochlorothiazide

Trial Details

FieldValue
Enrollment Target 80 participants
Start Date 2004-03
Est. Completion 2004-04
Phase Phase 1

Sponsor

Teva Pharmaceuticals USA

83 total trials

What the Registry Record Tells You About NCT01149473

The ClinicalTrials.gov registry entry for NCT01149473 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 80 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Teva Pharmaceuticals USA, which has 83 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Losartan potassium/Hydrochlorothiazide is the first listed.

NCT01149473 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01149473 about?

NCT01149473 is a clinical study titled "Losartan Potassium/Hydrochlorothiazide 100/25 mg Tablets in Healthy Subjects Under Non-Fasting Conditions". The objective of this study is to compare the relative bioavailability of Losartan potassium/Hydrochlorothiazide 100/25 mg tablets (manufactured by Teva Pharmaceutical Industries, Ltd. and distributed by Teva Pharmaceuticals USA) with that of Hyzaar® 100/25 mg tablets (Merck) in healthy, adult, non-...

What is the current status of trial NCT01149473?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 80 participants. The study started on 2004-03. Estimated completion is 2004-04.

What interventions are being tested in trial NCT01149473?

The interventions under investigation include: Losartan potassium/Hydrochlorothiazide (DRUG).

Who is sponsoring clinical trial NCT01149473?

This trial is sponsored by Teva Pharmaceuticals USA, which has 83 total clinical trials registered on ClinicalTrials.gov.

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.