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NCT00734292 · ClinicalTrials.gov registry record · Phase 2

Single-dose Crossover Study to Evaluate the Early Bronchodilating Effect of FlutiForm HFA pMDI in Adult Subjects With Mild to Moderate Asthma

A Phase 2 study, sponsored by SkyePharma.

Completed
Registry status
Phase 2
Development phase
39
Enrollment target

NCT00734292: Completed Phase 2 study, sponsored by SkyePharma.

NCT00734292 is a Phase 2 study that has completed, run by SkyePharma. The registered enrollment target is 39 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (71% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT00734292, a Phase 2 study, has completed, sponsored by SkyePharma.

COMPLETED
Registry status
Phase 2
Development phase
39 participants
Enrollment target

Study Summary

The primary purpose of this study is to evaluate the early bronchodilating effect of SKP FlutiForm HFA pMDI compared to placebo.

Interventions

  • DRUG fluticasone propionate, formoterol fumarate
  • OTHER fluticasone propionate, formoterol fumarate

Trial Details

FieldValue
Enrollment Target 39 participants
Start Date 2008-09
Est. Completion 2008-10
Phase Phase 2
SkyePharma

7 total trials

What the finished NCT00734292 record still lists

NCT00734292 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 39 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (71% lower).

The record links to 0 conditions, and to 2 interventions - of which fluticasone propionate, formoterol fumarate is the first listed.

NCT00734292 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00734292 about?

NCT00734292 is a clinical study titled "Single-dose Crossover Study to Evaluate the Early Bronchodilating Effect of FlutiForm HFA pMDI in Adult Subjects With Mild to Moderate Asthma". The primary purpose of this study is to evaluate the early bronchodilating effect of SKP FlutiForm HFA pMDI compared to placebo.

What is the current status of trial NCT00734292?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 39 participants. The study started on 2008-09. Estimated completion is 2008-10.

What interventions are being tested in trial NCT00734292?

The interventions under investigation include: fluticasone propionate, formoterol fumarate (DRUG), fluticasone propionate, formoterol fumarate (OTHER).

Who is sponsoring clinical trial NCT00734292?

This trial is sponsored by SkyePharma, which has 7 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00734292's enrollment target sits among peer trials

39 1459th of 2000 higher than 534 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 NCT00734292, the US trial registry maintained by the National Library of Medicine. NCT00734292 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.