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 @ 4:06 AM
Ignite Modification Date:
2025-12-26 @ 3:02 AM
NCT ID:
NCT03301220
Group ID:
EG000
Title:
Arm A: Active Monitoring (ACTM)
Description:
Participants in the active monitoring group did not receive any study medication but underwent disease evaluations for every 12 weeks until disease progression (PD) as those randomized to receive daratumumab.
Deaths Number Affected:
26
Deaths Number At Risk:
None
Serious Number Affected:
38
Serious Number At Risk:
196
Other Number Affected:
140
Other Number At Risk:
196
Study:
NCT03301220
Results Section:
NCT03301220
Adverse Events Module:
NCT03301220