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NCT02275481 · ClinicalTrials.gov registry record · Phase 4

A Study of Arformoterol Tartrate Inhalation Solution and Tiotropium Bromide on Re-hospitalization in Chronic Obstructive Pulmonary Disease (COPD) Subjects

A Phase 4 study, sponsored by Sumitomo Pharma America.

Terminated
Registry status
Phase 4
Development phase
66
Enrollment target

NCT02275481 is a Phase 4 study that was terminated before completion, run by Sumitomo Pharma America. The registered enrollment target is 66 participants.

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The verdict

NCT02275481, a Phase 4 study, was terminated before completion, sponsored by Sumitomo Pharma America.

TERMINATED
Registry status
Phase 4
Development phase
66 participants
Enrollment target

Study Summary

This is a randomized, open-label, parallel group, multicenter, outpatient study in COPD subjects who are discharged from the hospital due to a COPD exacerbation. Subjects who meet the eligibility criteria will be randomized to 1 of 2 treatments: arformoterol tartrate inhalation solution (BROVANA) 15 mcg twice daily (BID) or tiotropium bromide (SPIRIVA) 18 mcg once daily (QD), each given for 90 days.

Interventions

  • DRUG Tiotropium
  • DRUG Arformoterol tartrate inhalation solution

Trial Details

FieldValue
Enrollment Target 66 participants
Start Date 2014-11
Est. Completion 2016-09-14
Phase Phase 4

Sponsor

Sumitomo Pharma America

168 total trials

What the Registry Record Tells You About NCT02275481

The ClinicalTrials.gov registry entry for NCT02275481 describes a study currently listed as terminated, categorized as Phase 4. The registered enrollment target is 66 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Sumitomo Pharma America, which has 168 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Tiotropium is the first listed.

NCT02275481 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02275481 about?

NCT02275481 is a clinical study titled "A Study of Arformoterol Tartrate Inhalation Solution and Tiotropium Bromide on Re-hospitalization in Chronic Obstructive Pulmonary Disease (COPD) Subjects". This is a randomized, open-label, parallel group, multicenter, outpatient study in COPD subjects who are discharged from the hospital due to a COPD exacerbation. Subjects who meet the eligibility criteria will be randomized to 1 of 2 treatments: arformoterol tartrate inhalation solution (BROVANA) 15...

What is the current status of trial NCT02275481?

This trial is currently terminated. It is a Phase 4 study. The enrollment target is 66 participants. The study started on 2014-11. Estimated completion is 2016-09-14.

What interventions are being tested in trial NCT02275481?

The interventions under investigation include: Tiotropium (DRUG), Arformoterol tartrate inhalation solution (DRUG).

Who is sponsoring clinical trial NCT02275481?

This trial is sponsored by Sumitomo Pharma America, which has 168 total clinical trials registered on ClinicalTrials.gov.

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.