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 @ 4:05 PM
Ignite Modification Date:
2025-12-25 @ 2:06 PM
NCT ID:
NCT03101566
Group ID:
EG001
Title:
Nivolumab + Ipilimumab
Description:
Nivolumab 240 mg IV on day 1 every 2 weeks + Ipilimumab 1 mg/kg IV on day 1 every 6 weeks; for up to 2 years in absence of disease progression.
Deaths Number Affected:
23
Deaths Number At Risk:
None
Serious Number Affected:
23
Serious Number At Risk:
33
Other Number Affected:
28
Other Number At Risk:
33
Study:
NCT03101566
Results Section:
NCT03101566
Adverse Events Module:
NCT03101566