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Clinical Trials/NCT00103922
NCT00103922
Completed
Phase 3

A Randomized, 24-week, Double-blind, Placebo-controlled, Parallel-group Study to Evaluate the Efficacy, Safety and Tolerability of ARIFLO® (15mg BID) in Patients With Chronic Obstructive Pulmonary Disease (COPD)

GlaxoSmithKline1 site in 1 country600 target enrollmentNovember 2004

Overview

Phase
Phase 3
Intervention
cilomilast
Conditions
Pulmonary Disease, Chronic Obstructive
Sponsor
GlaxoSmithKline
Enrollment
600
Locations
1
Primary Endpoint
measure of lung function and quality of life in patients with COPD
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

This study was designed to determine if the investigational drug is effective and safe in individuals with COPD (chronic pulmonary disease)

Registry
clinicaltrials.gov
Start Date
November 2004
End Date
January 2007
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Arms & Interventions

Arm 1

Intervention: cilomilast

Outcomes

Primary Outcomes

measure of lung function and quality of life in patients with COPD

Secondary Outcomes

  • exacerbations in patients with COPD

Study Sites (1)

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