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 @ 12:44 AM
Ignite Modification Date:
2025-12-25 @ 10:57 PM
NCT ID:
NCT02643667
Group ID:
EG001
Title:
Safety Run-In and Phase II: Ibrutinib
Description:
* Ibrutinib 840 mg by mouth once daily for 4 weeks.
* Radical prostatectomy will be performed at least 7 days but not more than 12 days following the last scheduled dose of ibrutinib
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
5
Serious Number At Risk:
24
Other Number Affected:
24
Other Number At Risk:
24
Study:
NCT02643667
Results Section:
NCT02643667
Adverse Events Module:
NCT02643667