Event Group
Event Groups are part of the Adverse Events Module within the Results Section. They provide a way to organize and summarize adverse event data by grouping related events together.
Each Event Group typically represents a category or class of adverse events and includes statistical information such as the number of participants affected and at risk for different event types: deaths, serious events, and other events.
Event Group path is as follows:
Study -> Results Section -> Adverse Events Module -> Event Group
Event Group
Ignite Creation Date:
2025-12-24 @ 7:22 PM
Ignite Modification Date:
2025-12-25 @ 5:01 PM
NCT ID:
NCT01953003
Group ID:
EG000
Title:
Arm A : iv Vinflunine Plus Capecitabine
Description:
Vinflunine dose 280 mg/m² on day 1 of each cycle every 3 weeks, Capecitabine 825 mg/m² twice daily orally for 14 consecutive days beginning on day 1 of each cycle followed by 1 week of rest.
vinflunine: intraveinous administration day 1 once every 3 weeks, 280 mg/m²
Capecitabine: Arm A : 1650 mg/m² Arm B : 2500 mg/m²
Deaths Number Affected:
26
Deaths Number At Risk:
None
Serious Number Affected:
15
Serious Number At Risk:
56
Other Number Affected:
54
Other Number At Risk:
56
Study:
NCT01953003
Results Section:
NCT01953003
Adverse Events Module:
NCT01953003