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 @ 12:22 PM
Ignite Modification Date:
2025-12-25 @ 12:03 PM
NCT ID:
NCT02187861
Group ID:
EG002
Title:
Chemotherapy-Containing Cohort: Arm B (Venetoclax + BR)
Description:
Participants received venetoclax 800 mg orally once daily continuously for 1 year along with rituximab 375 mg/m\^2 IV infusion on Day 1 of each 28-day cycle and bendamustine 90 mg/m\^2 IV infusion on Days 1 and 2 of each 28-day cycle, for 6 cycles.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
26
Serious Number At Risk:
49
Other Number Affected:
49
Other Number At Risk:
49
Study:
NCT02187861
Results Section:
NCT02187861
Adverse Events Module:
NCT02187861