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 @ 1:15 PM
Ignite Modification Date:
2025-12-25 @ 12:24 PM
NCT ID:
NCT03597295
Group ID:
EG000
Title:
Retifanlimab 500 mg
Description:
Participants received retifanlimab 500 milligrams (mg) intravenously every 4 weeks (Q4W).
Deaths Number Affected:
60
Deaths Number At Risk:
None
Serious Number Affected:
50
Serious Number At Risk:
94
Other Number Affected:
79
Other Number At Risk:
94
Study:
NCT03597295
Results Section:
NCT03597295
Adverse Events Module:
NCT03597295