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NCT01168310 · ClinicalTrials.gov registry record · Phase 2

A Trial to Assess the Pharmacodynamic Response in Subjects With Chronic Obstructive Pulmonary Disease (COPD)

A Phase 2 study, sponsored by Dey.

Completed
Registry status
Phase 2
Development phase
468
Enrollment target

NCT01168310: Completed Phase 2 study, sponsored by Dey.

NCT01168310 is a Phase 2 study that has completed, run by Dey. The registered enrollment target is 468 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (252% higher). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT01168310, a Phase 2 study, has completed, sponsored by Dey.

COMPLETED
Registry status
Phase 2
Development phase
468 participants
Enrollment target

Study Summary

This is a randomized, double-blind, multi-dose, parallel group trial which will assess the pharmacodynamic response of fluticasone propionate and formoterol fumarate in subjects with COPD.

Interventions

  • DRUG Fluticasone Propionate/Formoterol Fumarate

Trial Details

FieldValue
Enrollment Target 468 participants
Start Date 2010-08
Est. Completion 2011-10
Phase Phase 2
Dey

21 total trials

What the finished NCT01168310 record still lists

NCT01168310 is an interventional study that assigns participants to a tested intervention. The registered 468 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (252% higher).

The record links to 0 conditions, and to 1 intervention - of which Fluticasone Propionate/Formoterol Fumarate is the first listed.

NCT01168310 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01168310 about?

NCT01168310 is a clinical study titled "A Trial to Assess the Pharmacodynamic Response in Subjects With Chronic Obstructive Pulmonary Disease (COPD)". This is a randomized, double-blind, multi-dose, parallel group trial which will assess the pharmacodynamic response of fluticasone propionate and formoterol fumarate in subjects with COPD.

What is the current status of trial NCT01168310?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 468 participants. The study started on 2010-08. Estimated completion is 2011-10.

What interventions are being tested in trial NCT01168310?

The interventions under investigation include: Fluticasone Propionate/Formoterol Fumarate (DRUG).

Who is sponsoring clinical trial NCT01168310?

This trial is sponsored by Dey, which has 21 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01168310's enrollment target sits among peer trials

468 80th of 2000 higher than 1,921 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 NCT01168310, the US trial registry maintained by the National Library of Medicine. NCT01168310 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.