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 @ 3:07 AM
Ignite Modification Date:
2025-12-26 @ 1:46 AM
NCT ID:
NCT00833833
Group ID:
EG006
Title:
Phase 2: Pomalidomide (Pom + Dex Only)
Description:
Pomalidomide 4 mg daily on days 1-21 of each 28-day cycle. Upon PD, participants had the option of discontinuing therapy or adding dexamethasone.
Data are reported during the time after PD when participants were on both pomalidomide and dexamethasone.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
29
Serious Number At Risk:
61
Other Number Affected:
57
Other Number At Risk:
61
Study:
NCT00833833
Results Section:
NCT00833833
Adverse Events Module:
NCT00833833