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 @ 12:12 AM
Ignite Modification Date:
2025-12-25 @ 10:14 PM
NCT ID:
NCT01858558
Group ID:
EG000
Title:
aMIL Arm
Description:
Patients receive activated Marrow Infiltrating Lymphocytes (aMIL)
aMIL: On day 0, patients will receive auto transplant followed by Tadalafil and aMIL. At day 60, patients will receive Lenalidomide.
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
64
Serious Number At Risk:
70
Other Number Affected:
11
Other Number At Risk:
70
Study:
NCT01858558
Results Section:
NCT01858558
Adverse Events Module:
NCT01858558