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 @ 2:39 AM
Ignite Modification Date:
2025-12-26 @ 1:17 AM
NCT ID:
NCT05044234
Group ID:
EG003
Title:
375 mg Cedirogant
Description:
Participants received 375 mg cedirogant orally once daily (QD) for 16 weeks.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
2
Serious Number At Risk:
39
Other Number Affected:
16
Other Number At Risk:
39
Study:
NCT05044234
Results Section:
NCT05044234
Adverse Events Module:
NCT05044234