drugset / Trial / NCT00242294

Efficacy and Safety of Roflumilast in Japanese Patients Older Than 40 Years With Chronic Obstructive Pulmonary Disease (APTA-2217-06)

NCT00242294

Phase 2/3 Completed 570 enrolled AstraZeneca Tanabe Pharma Corporation · collab
RandomizedParallel-groupDouble-blindTreatment

Summary

The aim of the study is to investigate the effect of roflumilast (APTA-2217) on lung function in patients with chronic obstructive pulmonary disease (COPD). Roflumilast will be administered orally once daily. The study duration consists of a baseline period (4 weeks) and a treatment period (24 weeks). The study will provide further data on safety, tolerability, and effectiveness of roflumilast.

Timeline

Start
2004-11
Primary completion
2006-09
Completion
2007-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Roflumilast Small molecule Oral