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:
2025-12-25 @ 2:11 AM
Ignite Modification Date:
2025-12-26 @ 12:39 AM
NCT ID:
NCT03472560
Group ID:
EG001
Title:
UC Avelumab + Axitinib
Description:
Participants received avelumab 800 mg intravenous dose every two weeks, (Day 1 and 15) of each 28-day cycle in combination with axitinib 5 mg twice daily dose on a continuous dosing schedule.
Deaths Number Affected:
11
Deaths Number At Risk:
None
Serious Number Affected:
11
Serious Number At Risk:
20
Other Number Affected:
17
Other Number At Risk:
20
Study:
NCT03472560
Results Section:
NCT03472560
Adverse Events Module:
NCT03472560