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 @ 2:42 AM
Ignite Modification Date:
2025-12-26 @ 1:21 AM
NCT ID:
NCT05483933
Group ID:
EG001
Title:
Mirvetuximab + SL-172154
Description:
3.0 mg/kg SL-172154 on Days 8 and 15 of every 21-day cycle plus mirvetuximab (MIRV) 6.0 mg/kg on Day 1 of every 21-day cycle
Deaths Number Affected:
30
Deaths Number At Risk:
None
Serious Number Affected:
17
Serious Number At Risk:
65
Other Number Affected:
65
Other Number At Risk:
65
Study:
NCT05483933
Results Section:
NCT05483933
Adverse Events Module:
NCT05483933