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 @ 2:46 PM
Ignite Modification Date:
2025-12-25 @ 1:15 PM
NCT ID:
NCT01721759
Group ID:
EG000
Title:
Nivolumab, 3 mg/kg
Description:
Participants received nivolumab, 3 mg/kg, intravenously over 60 minutes every 2 weeks (on Day 1 of each cycle) until disease progression, discontinuation due to toxicity, withdrawal of consent, or end of study. Every 2-week treatment period was considered to be a cycle.
Deaths Number Affected:
108
Deaths Number At Risk:
None
Serious Number Affected:
88
Serious Number At Risk:
117
Other Number Affected:
110
Other Number At Risk:
117
Study:
NCT01721759
Results Section:
NCT01721759
Adverse Events Module:
NCT01721759