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 @ 1:02 AM
Ignite Modification Date:
2025-12-25 @ 11:15 PM
NCT ID:
NCT03873493
Group ID:
EG000
Title:
Venetoclax + Ibrutinib
Description:
Participants received 400 mg venetoclax orally once a day after a 5-day ramp-up and 420 mg ibrutinib orally once a day for up to 2 years or until progressive disease, intolerability, or they became eligible for stem cell transplantation after achieving complete remission.
Deaths Number Affected:
10
Deaths Number At Risk:
None
Serious Number Affected:
8
Serious Number At Risk:
14
Other Number Affected:
14
Other Number At Risk:
14
Study:
NCT03873493
Results Section:
NCT03873493
Adverse Events Module:
NCT03873493