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 @ 10:55 PM
Ignite Modification Date:
2025-12-25 @ 8:23 PM
NCT ID:
NCT04373369
Group ID:
EG000
Title:
Vorolanib + Atezolizumab
Description:
Consenting and eligible participants who have no evidence of tumor progression after 3 to 4 cycles of standard-of-care induction therapy will receive atezolizumab intravenously (IV) every 3 weeks and vorolanib by mouth daily.
Deaths Number Affected:
8
Deaths Number At Risk:
None
Serious Number Affected:
3
Serious Number At Risk:
11
Other Number Affected:
11
Other Number At Risk:
11
Study:
NCT04373369
Results Section:
NCT04373369
Adverse Events Module:
NCT04373369