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NCT02512510 · ClinicalTrials.gov registry record · Phase 3

Efficacy Study of Nebulized TD-4208 for Chronic Obstructive Pulmonary Disease (COPD)

A Phase 3 study of Chronic Obstructive Pulmonary Disease (COPD), sponsored by Mylan.

Completed
Registry status
Phase 3
Development phase
611
Enrollment target
1
Study location

NCT02512510 is a Phase 3 study of Chronic Obstructive Pulmonary Disease (COPD) that has completed, run by Mylan. The registered enrollment target is 611 participants, roughly in line with the 634-participant average among 36 other Chronic Obstructive Pulmonary Disease (COPD) trials with a reported enrollment target. The trial reports 1 study location across 1 state.

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The verdict

NCT02512510, a Phase 3 study of Chronic Obstructive Pulmonary Disease (COPD), has completed, sponsored by Mylan.

COMPLETED
Registry status
Phase 3
Development phase
611 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to measure the effectiveness and safety of TD 4208, an investigational drug being developed to treat people with moderate to very severe COPD, compared to placebo, a treatment without activity.

Interventions

  • DRUG Placebo
  • DRUG TD-4208

Study Locations (1)

South Carolina

  • Palmetto Medical Research Associates L.L.C. - Easley

Trial Details

FieldValue
Enrollment Target 611 participants
Start Date 2015-09
Est. Completion 2016-09
Phase Phase 3

Sponsor

Mylan

22 total trials

What the Registry Record Tells You About NCT02512510

The ClinicalTrials.gov registry entry for NCT02512510 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 611 participants, a figure that helps gauge the scale of data the investigators plan to collect, roughly in line with the 634-participant average among 36 other Chronic Obstructive Pulmonary Disease (COPD) trials with a reported enrollment target. The listed sponsor is Mylan, which has 22 total studies on file at ClinicalTrials.gov.

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

NCT02512510 reports 1 study location spanning 1 distinct geographic area - top geographies include South Carolina.

Frequently Asked Questions

What is clinical trial NCT02512510 about?

NCT02512510 is a clinical study titled "Efficacy Study of Nebulized TD-4208 for Chronic Obstructive Pulmonary Disease (COPD)". The purpose of this study is to measure the effectiveness and safety of TD 4208, an investigational drug being developed to treat people with moderate to very severe COPD, compared to placebo, a treatment without activity.

What is the current status of trial NCT02512510?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 611 participants. The study started on 2015-09. Estimated completion is 2016-09.

What conditions does trial NCT02512510 study?

This clinical trial studies the following conditions: Chronic Obstructive Pulmonary Disease (COPD).

What interventions are being tested in trial NCT02512510?

The interventions under investigation include: Placebo (DRUG), TD-4208 (DRUG).

Who is sponsoring clinical trial NCT02512510?

This trial is sponsored by Mylan, which has 22 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02512510 being conducted?

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

Similar trials for Chronic Obstructive Pulmonary Disease (COPD)

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

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.