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NCT00749411 · ClinicalTrials.gov registry record · Phase 2

Safety and Tolerability of Repeat Dosing of GSK233705/GW642444 in COPD

A Phase 2 study of Pulmonary Disease, Chronic Obstructive, sponsored by GlaxoSmithKline.

Completed
Registry status
Phase 2
Development phase
61
Enrollment target
12
Study locations

NCT00749411 is a Phase 2 study of Pulmonary Disease, Chronic Obstructive that has completed, run by GlaxoSmithKline. The registered enrollment target is 61 participants, below the 1,043-participant average among 74 other Pulmonary Disease, Chronic Obstructive trials with a reported enrollment target (94% lower). The trial reports 12 study locations across 11 states.

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The verdict

NCT00749411, a Phase 2 study of Pulmonary Disease, Chronic Obstructive, has completed, sponsored by GlaxoSmithKline.

COMPLETED
Registry status
Phase 2
Development phase
61 participants
Enrollment target
12
Study locations

Study Summary

The purpose of this study is the evaluate the safety and tolerability of repeat dosing of the combination of inhaled GSK233705 and GW642444 administered once-daily in subjects with COPD.

Interventions

  • DRUG Placebo
  • DRUG GSK233705/GW642444

Study Locations (12)

South Carolina

  • GSK Investigational Site - Greenville
  • GSK Investigational Site - Spartanburg

Alabama

  • GSK Investigational Site - Mobile

Colorado

  • GSK Investigational Site - Wheat Ridge

Maine

  • GSK Investigational Site - Biddeford

Missouri

  • GSK Investigational Site - St Louis

New Jersey

  • GSK Investigational Site - Summit

Oregon

  • GSK Investigational Site - Medford

Pennsylvania

  • GSK Investigational Site - Erie

Trial Details

FieldValue
Enrollment Target 61 participants
Start Date 2008-11-13
Est. Completion 2009-02-12
Phase Phase 2

Sponsor

GlaxoSmithKline

1,345 total trials

What the Registry Record Tells You About NCT00749411

The ClinicalTrials.gov registry entry for NCT00749411 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 61 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,043-participant average among 74 other Pulmonary Disease, Chronic Obstructive trials with a reported enrollment target (94% lower). The listed sponsor is GlaxoSmithKline, which has 1,345 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Pulmonary Disease, Chronic Obstructive appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT00749411 reports 12 study locations spanning 11 distinct geographic areas - top geographies include South Carolina, Alabama, Colorado.

Frequently Asked Questions

What is clinical trial NCT00749411 about?

NCT00749411 is a clinical study titled "Safety and Tolerability of Repeat Dosing of GSK233705/GW642444 in COPD". The purpose of this study is the evaluate the safety and tolerability of repeat dosing of the combination of inhaled GSK233705 and GW642444 administered once-daily in subjects with COPD.

What is the current status of trial NCT00749411?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 61 participants. The study started on 2008-11-13. Estimated completion is 2009-02-12.

What conditions does trial NCT00749411 study?

This clinical trial studies the following conditions: Pulmonary Disease, Chronic Obstructive.

What interventions are being tested in trial NCT00749411?

The interventions under investigation include: Placebo (DRUG), GSK233705/GW642444 (DRUG).

Who is sponsoring clinical trial NCT00749411?

This trial is sponsored by GlaxoSmithKline, which has 1,345 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00749411 being conducted?

This trial has 12 study locations across Alabama, Colorado, Maine, Missouri, New Jersey. 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, or report a data error.