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NCT00909779 · ClinicalTrials.gov registry record · Phase 3

Safety Study of Arformoterol Tartrate Inhalation Solution in Chronic Obstructive Pulmonary Disease (COPD) Subjects

A Phase 3 study, sponsored by Sumitomo Pharma America.

Completed
Registry status
Phase 3
Development phase
841
Enrollment target

NCT00909779: Completed Phase 3 study, sponsored by Sumitomo Pharma America.

NCT00909779 is a Phase 3 study that has completed, run by Sumitomo Pharma America. The registered enrollment target is 841 participants, roughly in line with the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00909779, a Phase 3 study, has completed, sponsored by Sumitomo Pharma America.

COMPLETED
Registry status
Phase 3
Development phase
841 participants
Enrollment target

Study Summary

This is a multi-center study to evaluate the long-term safety of arformoterol 15 mcg twice daily (BID) in the treatment of subjects with moderate-to-severe COPD. Study participation will consist of a total of 6 visits over approximately 1 year.

Primary Outcome

COPD exacerbation: an increase in COPD symptoms that necessitated any change in baseline medication (bronchodilators,anti-inflammatory agents, antibiotics, supplemental oxygen therapy, etc.).Hospitalization: any inpatient admission or any emergency department visit \> 24 hours in duration. Hospice was considered hospitalization.COPD exacerbation related hospitalization: hospitalization that was due to 1) COPD exacerbation or 2) a COPD exacerbation preceded, or occurred concomitantly with the ons

Interventions

  • DRUG Placebo
  • DRUG Arformoterol

Trial Details

FieldValue
Enrollment Target 841 participants
Start Date 2009-06
Est. Completion 2012-06
Phase Phase 3
Sumitomo Pharma America

168 total trials

What the finished NCT00909779 record still lists

NCT00909779 is an interventional study that assigns participants to a tested intervention. The registered 841 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target.

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

NCT00909779 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00909779 about?

NCT00909779 is a clinical study titled "Safety Study of Arformoterol Tartrate Inhalation Solution in Chronic Obstructive Pulmonary Disease (COPD) Subjects". This is a multi-center study to evaluate the long-term safety of arformoterol 15 mcg twice daily (BID) in the treatment of subjects with moderate-to-severe COPD. Study participation will consist of a total of 6 visits over approximately 1 year.

What is the current status of trial NCT00909779?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 841 participants. The study started on 2009-06. Estimated completion is 2012-06.

What interventions are being tested in trial NCT00909779?

The interventions under investigation include: Placebo (DRUG), Arformoterol (DRUG).

Who is sponsoring clinical trial NCT00909779?

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

How this trial's enrollment target compares

Where NCT00909779's enrollment target sits among peer trials

841 392nd of 2000 higher than 1,609 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00909779, the US trial registry maintained by the National Library of Medicine. NCT00909779 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.