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 @ 11:58 PM
Ignite Modification Date:
2025-12-25 @ 9:56 PM
NCT ID:
NCT04419558
Group ID:
EG002
Title:
OLE Period: Pamrevlumab
Description:
Participants who completed the treatment in DB period and entered in the OLE period, received pamrevlumab 30 mg/kg administered by IV infusion, every 3 weeks for up to 48 weeks.
Deaths Number Affected:
12
Deaths Number At Risk:
None
Serious Number Affected:
20
Serious Number At Risk:
86
Other Number Affected:
21
Other Number At Risk:
86
Study:
NCT04419558
Results Section:
NCT04419558
Adverse Events Module:
NCT04419558