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NCT00834873 · ClinicalTrials.gov registry record · Phase 1

Carvedilol (25 mg) in 24 Fed, Healthy, Adult Subjects

A Phase 1 study, sponsored by Teva Pharmaceuticals USA.

Completed
Registry status
Phase 1
Development phase
24
Enrollment target

NCT00834873: Completed Phase 1 study, sponsored by Teva Pharmaceuticals USA.

NCT00834873 is a Phase 1 study that has completed, run by Teva Pharmaceuticals USA. The registered enrollment target is 24 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00834873, a Phase 1 study, has completed, sponsored by Teva Pharmaceuticals USA.

COMPLETED
Registry status
Phase 1
Development phase
24 participants
Enrollment target

Study Summary

The objective of this randomized, single-dose, two-way crossover evaluation is to compare the relative bioequivalence of a test carvedilol formulation (TEVA Pharmaceuticals USA) to and equivalent oral dose of the commercially available carvedilol (COREG®, SmithKline Beecham Pharmaceuticals) in a test population of 24 adult individuals under fed conditions.

Interventions

  • DRUG Carvedilol 25 mg tablets
  • DRUG COREG® 25 mg tablets

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2001-12
Est. Completion 2001-12
Phase Phase 1

Sponsor

Teva Pharmaceuticals USA

83 total trials

What the Registry Record Tells You About NCT00834873

The ClinicalTrials.gov registry entry for NCT00834873 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 24 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 2 interventions - of which Carvedilol 25 mg tablets is the first listed.

NCT00834873 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00834873 about?

NCT00834873 is a clinical study titled "Carvedilol (25 mg) in 24 Fed, Healthy, Adult Subjects". The objective of this randomized, single-dose, two-way crossover evaluation is to compare the relative bioequivalence of a test carvedilol formulation (TEVA Pharmaceuticals USA) to and equivalent oral dose of the commercially available carvedilol (COREG®, SmithKline Beecham Pharmaceuticals) in a tes...

What is the current status of trial NCT00834873?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 24 participants. The study started on 2001-12. Estimated completion is 2001-12.

What interventions are being tested in trial NCT00834873?

The interventions under investigation include: Carvedilol 25 mg tablets (DRUG), COREG® 25 mg tablets (DRUG).

Who is sponsoring clinical trial NCT00834873?

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.