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:
EG000
Title:
DB Period: Pamrevlumab
Description:
Participants received pamrevlumab 30 mg/kg, administered by IV infusion, every 3 weeks, for a total of up to 17 infusions over 48 weeks in the DB period.
Deaths Number Affected:
16
Deaths Number At Risk:
None
Serious Number Affected:
38
Serious Number At Risk:
183
Other Number Affected:
83
Other Number At Risk:
183
Study:
NCT04419558
Results Section:
NCT04419558
Adverse Events Module:
NCT04419558