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 @ 2:40 AM
Ignite Modification Date:
2025-12-26 @ 1:19 AM
NCT ID:
NCT04187833
Group ID:
EG000
Title:
Nivolumab + Talazoparib
Description:
Nivolumab 480mg intravenously every 4 weeks (28 days) + Talazoparib 1mg orally daily
Nivolumab: 480mg intravenously every 4 weeks (28 days)
Talazoparib: 1mg orally daily
Deaths Number Affected:
7
Deaths Number At Risk:
None
Serious Number Affected:
1
Serious Number At Risk:
8
Other Number Affected:
8
Other Number At Risk:
8
Study:
NCT04187833
Results Section:
NCT04187833
Adverse Events Module:
NCT04187833