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 @ 2:33 AM
Ignite Modification Date:
2025-12-26 @ 1:09 AM
NCT ID:
NCT01358734
Group ID:
EG001
Title:
Azacitidine Plus Lenalidomide
Description:
Participants received azacitidine 75 mg/m\^2/ QD administered subcutaneously (SC) on Days 1 through 7 and lenalidomide 50 mg QD PO on days 8 through 28 followed by a 14-day rest period plus BSC
Deaths Number Affected:
34
Deaths Number At Risk:
None
Serious Number Affected:
29
Serious Number At Risk:
38
Other Number Affected:
38
Other Number At Risk:
38
Study:
NCT01358734
Results Section:
NCT01358734
Adverse Events Module:
NCT01358734