Clinical Trial Results:
A single dose, placebo-controlled, randomized, double-blind, double-dummy, crossover efficacy, pharmacokinetics and safety comparison of salmeterol inhalation powder (12.5 µg, 25 µg and 50 µg salmeterol), administered as the xinafoate salt from hard polyethylene capsules via the HandiHaler(R) 2, and Serevent(R) Diskus(R) (50 µg salmeterol) in patients with chronic obstructive pulmonary disease (COPD)
Summary
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EudraCT number |
2005-000918-13 |
Trial protocol |
DE |
Global completion date |
07 Feb 2006
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Paediatric regulatory details
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Is the trial part of an agreed EMA paediatric investigation plan? |
No
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Is the trial in scope of article 45 of Regulation (EC) No 1901/2006? |
No
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Is the trial in scope of article 46 of Regulation (EC) No 1901/2006? |
No
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Results information
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Results version number |
v1(current) |
This version publication date |
04 Mar 2016
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First version publication date |
04 Mar 2016
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Other versions |
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Summary report(s) |
Trial Synopsis |
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.