- ICH GCP
- EU: s kliniska prövningsregister
Kliniska prövningar Nct sida
Clinical Trial Results:
A Randomized, Double-Blind, Parallel-Group Study Conducted Under In-House Blinding Conditions to Determine the Efficacy and Tolerability of Aprepitant for the Prevention of Chemotherapy-Induced Nausea and Vomiting Associated With Moderately Emetogenic Chemotherapy (Study #2)
Summary | |
EudraCT number | 2006-003512-22 |
Trial protocol | FR DE |
Global completion date | 19 Nov 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 Apr 2016 |
First version publication date | 16 Apr 2016 |
Other versions | |
Summary report(s) | clinicaltrials.gov record including results |
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.