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 @ 6:26 PM
Ignite Modification Date:
2025-12-25 @ 3:56 PM
NCT ID:
NCT02119468
Group ID:
EG001
Title:
Dose Level #2 (4mg MLN9708)
Description:
Patients receive 4mg ixazomib citrate (MLN9708) orally on days 1, 8, and 15; dexamethasone orally on days 1, 8, 15, and 22; and pomalidomide orally on days 1-21. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.
ixazomib citrate: Given orally
dexamethasone: Given orally
pomalidomide: Given orally
Deaths Number Affected:
6
Deaths Number At Risk:
None
Serious Number Affected:
11
Serious Number At Risk:
25
Other Number Affected:
25
Other Number At Risk:
25
Study:
NCT02119468
Results Section:
NCT02119468
Adverse Events Module:
NCT02119468