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 @ 7:50 PM
Ignite Modification Date:
2025-12-25 @ 5:26 PM
NCT ID:
NCT00508404
Group ID:
EG000
Title:
Panitumumab Plus FOLFIRI
Description:
Participants received 6 mg/kg panitumumab intravenously (IV) once every 14 days in combination with FOLFIRI chemotherapy regimen consisting of irinotecan, infusional 5-fluorouracil, and leucovorin, until diagnosed with radiographic disease progression.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
84
Serious Number At Risk:
154
Other Number Affected:
154
Other Number At Risk:
154
Study:
NCT00508404
Results Section:
NCT00508404
Adverse Events Module:
NCT00508404