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 @ 3:53 AM
Ignite Modification Date:
2025-12-26 @ 2:42 AM
NCT ID:
NCT02599402
Group ID:
EG007
Title:
Nivolumab + Ipilimumab Acral
Description:
Nivolumab 1 mg/kg IV + Ipilimumab 3 mg/kg IV Q3W x 4 doses up to 3 months
Then
Part 2: Nivolumab (3mg/kg or 240mg) IV Q2W up to 21 months
Participants were grouped in to Disease Subtype subgroup Acral
Deaths Number Affected:
6
Deaths Number At Risk:
None
Serious Number Affected:
9
Serious Number At Risk:
10
Other Number Affected:
10
Other Number At Risk:
10
Study:
NCT02599402
Results Section:
NCT02599402
Adverse Events Module:
NCT02599402