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:
2025-12-24 @ 10:13 PM
Ignite Modification Date:
2025-12-25 @ 7:48 PM
NCT ID:
NCT03639935
Group ID:
EG000
Title:
Rucaparib and Nivolumab
Description:
Rucaparib 600 mg PO BID days 1-28 Nivolumab 240 mg IV days 1 and 15
Rucaparib: Rucaparib 600 mg PO BID days 1-28
Nivolumab: Nivolumab 240 mg IV days 1 and 15
Deaths Number Affected:
26
Deaths Number At Risk:
None
Serious Number Affected:
17
Serious Number At Risk:
31
Other Number Affected:
28
Other Number At Risk:
31
Study:
NCT03639935
Results Section:
NCT03639935
Adverse Events Module:
NCT03639935