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 @ 2:44 AM
Ignite Modification Date:
2025-12-26 @ 1:24 AM
NCT ID:
NCT04987333
Group ID:
EG003
Title:
Group 4: Caucasian Participants - Efavaleukin Alfa (Dose Level 2)
Description:
Caucasian participants who received efavaleukin alfa administered as one SC injection at dose level 2 (high).
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
8
Other Number Affected:
8
Other Number At Risk:
8
Study:
NCT04987333
Results Section:
NCT04987333
Adverse Events Module:
NCT04987333