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 @ 6:34 PM
Ignite Modification Date:
2025-12-25 @ 4:04 PM
NCT ID:
NCT03372057
Group ID:
EG002
Title:
Expansion Phase
Description:
Duvelisib PO BID at a starting dose of 75 mg for the first 2 cycles, followed by a mandatory reduction to 25 mg BID thereafter for those participants with CR, PR or SD, in 28-day cycles (dose determined in Optimization Phase).
Deaths Number Affected:
78
Deaths Number At Risk:
None
Serious Number Affected:
60
Serious Number At Risk:
123
Other Number Affected:
121
Other Number At Risk:
123
Study:
NCT03372057
Results Section:
NCT03372057
Adverse Events Module:
NCT03372057