Clinical Trial Results:
A 48-WEEK, DOUBLE BLIND, DOUBLE DUMMY, RANDOMISED, MULTINATIONAL, MULTICENTRE, 3-ARM PARALLEL GROUP CLINICAL STUDY OF “FIXED COMBINATION” BECLOMETHASONE DIPROPIONATE PLUS FORMOTEROL FUMARATE ADMINISTERED VIA pMDI WITH HFA-134a PROPELLANT (CHF 1535) VERSUS “FIXED COMBINATION” BUDESONIDE PLUS FORMOTEROL DPI (SYMBICORT® TURBOHALER®, ASTRAZENECA) VERSUS FORMOTEROL DPI (OXIS® TURBOHALER®, ASTRAZENECA) IN PATIENTS WITH STABLE SEVERE CHRONIC OBSTRUCTIVE PULMONARY DISEASE (COPD)
Summary
|
|
EudraCT number |
2006-002489-20 |
Trial protocol |
GB IT |
Global completion date |
07 Aug 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 |
06 Jan 2017
|
First version publication date |
06 Jan 2017
|
Other versions |
|
Summary report(s) |
EudraCT No. 2006-002489-20 Medical Journal Article |
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.