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:
2025-12-25 @ 12:43 AM
Ignite Modification Date:
2025-12-25 @ 10:55 PM
NCT ID:
NCT03163667
Group ID:
EG001
Title:
CB-839 + Everolimus
Description:
CB-839 oral tablets BID in combination with standard QD everolimus in 28 day cycles.
Deaths Number Affected:
27
Deaths Number At Risk:
None
Serious Number Affected:
21
Serious Number At Risk:
46
Other Number Affected:
45
Other Number At Risk:
46
Study:
NCT03163667
Results Section:
NCT03163667
Adverse Events Module:
NCT03163667