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:
2025-12-26 @ 5:18 PM
Ignite Modification Date:
2025-12-26 @ 5:18 PM
NCT ID:
NCT00877006
Group ID:
EG000
Title:
Bendamustine and Rituximab (BR)
Description:
Participants received the investigational bendamustine and rituximab regimen for 6 to 8 28-day cycles: bendamustine 90 mg/m\^2 intravenous (IV) on Days 1 and 2; rituximab 375 mg/m\^2 IV on Day 1.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
60
Serious Number At Risk:
221
Other Number Affected:
216
Other Number At Risk:
221
Study:
NCT00877006
Results Section:
NCT00877006
Adverse Events Module:
NCT00877006