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 @ 3:18 PM
Ignite Modification Date:
2025-12-25 @ 1:39 PM
NCT ID:
NCT00457392
Group ID:
EG000
Title:
Sunitinib + Erlotinib
Description:
Sunitinib capsule administered orally at a dose of 37.5 milligram (mg) daily (continuous regimen) in a 4 week cycle. Erlotinib administered orally at a dose of 150 mg daily.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
207
Serious Number At Risk:
473
Other Number Affected:
463
Other Number At Risk:
473
Study:
NCT00457392
Results Section:
NCT00457392
Adverse Events Module:
NCT00457392