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 @ 11:53 PM
Ignite Modification Date:
2025-12-25 @ 9:49 PM
NCT ID:
NCT01127451
Group ID:
EG001
Title:
Denileukin Diftitox on Days 1, 8, and 15
Description:
Participants received Denileukin Diftitox 12 mcg/kg/day on Days 1, 8 and 15 of 21-day treatment cycle for a total of 4 cycles (12 weeks) or until unacceptable toxicity or rapid and life-threatening progressive disease.
Deaths Number Affected:
17
Deaths Number At Risk:
None
Serious Number Affected:
8
Serious Number At Risk:
32
Other Number Affected:
9
Other Number At Risk:
32
Study:
NCT01127451
Results Section:
NCT01127451
Adverse Events Module:
NCT01127451