Clinical Trial Results:
Randomised, Double-Blind, Placebo-Controlled, Parallel Group Study
to Assess the Efficacy and Safety of 4 Weeks of Once Daily Treatment
of Orally Inhaled BI 1744 CL (2 µg, 5 µg, 10 µg, 20 µg) Delivered by
the Respimat® Inhaler in Patients with COPD
Summary
|
|
EudraCT number |
2006-004828-36 |
Trial protocol |
NL DE |
Global completion date |
14 Jan 2008
|
Paediatric regulatory details
|
|
Is the trial part of an agreed EMA paediatric investigation plan? |
No
|
Is the trial in scope of article 45 of Regulation (EC) No 1901/2006? |
No
|
Is the trial in scope of article 46 of Regulation (EC) No 1901/2006? |
No
|
Results information
|
|
Results version number |
v1(current) |
This version publication date |
16 May 2016
|
First version publication date |
05 Apr 2015
|
Other versions |
|
Summary report(s) |
1222.5 |
Note: The legislation allows summary attachments to be posted instead of the full dataset for this trial. Refer to Commission Guideline 2012/C 302/03
for further information.