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 @ 5:41 PM
Ignite Modification Date:
2025-12-25 @ 3:10 PM
NCT ID:
NCT00065468
Group ID:
EG001
Title:
Temsirolimus
Description:
Temsirolimus (CCI-779) 25 milligrams (mg) intravenously (IV) once per week until disease progression or treatment withdrawal
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
82
Serious Number At Risk:
208
Other Number Affected:
208
Other Number At Risk:
208
Study:
NCT00065468
Results Section:
NCT00065468
Adverse Events Module:
NCT00065468