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NCT00782535 · ClinicalTrials.gov registry record · Phase 2

Safety and Efficacy Study of Treatment With Single Doses of CHF 4226 pMDI in Patients With Chronic Obstructive Pulmonary Disease (COPD)

A Phase 2 study, sponsored by Chiesi Farmaceutici S.p.A..

Completed
Registry status
Phase 2
Development phase
20
Enrollment target

NCT00782535: Completed Phase 2 study, sponsored by Chiesi Farmaceutici S.p.A..

NCT00782535 is a Phase 2 study that has completed, run by Chiesi Farmaceutici S.p.A.. The registered enrollment target is 20 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (85% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00782535, a Phase 2 study, has completed, sponsored by Chiesi Farmaceutici S.p.A..

COMPLETED
Registry status
Phase 2
Development phase
20 participants
Enrollment target

Study Summary

The purpose of this study is to characterize the dose-response profile of peak and trough FEV1 after single dose administrations of carmoterol in patients with COPD.

Interventions

  • DRUG Placebo
  • DRUG CHF 4226 pMDI

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2008-12
Est. Completion 2009-03
Phase Phase 2
Chiesi Farmaceutici S.p.A.

30 total trials

What the finished NCT00782535 record still lists

NCT00782535 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (85% lower).

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

NCT00782535 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00782535 about?

NCT00782535 is a clinical study titled "Safety and Efficacy Study of Treatment With Single Doses of CHF 4226 pMDI in Patients With Chronic Obstructive Pulmonary Disease (COPD)". The purpose of this study is to characterize the dose-response profile of peak and trough FEV1 after single dose administrations of carmoterol in patients with COPD.

What is the current status of trial NCT00782535?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 20 participants. The study started on 2008-12. Estimated completion is 2009-03.

What interventions are being tested in trial NCT00782535?

The interventions under investigation include: Placebo (DRUG), CHF 4226 pMDI (DRUG).

Who is sponsoring clinical trial NCT00782535?

This trial is sponsored by Chiesi Farmaceutici S.p.A., which has 30 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00782535's enrollment target sits among peer trials

20 1805th of 2000 higher than 107 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT00782535, the US trial registry maintained by the National Library of Medicine. NCT00782535 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.