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:
EG007
Title:
Phase 2: Pomalidomide (Overall)
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 entire study up to the data cut-off, thus including both the time participants were only on pomalidomide and the time after PD when participants were on pomalidomide and dexamethasone.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
72
Serious Number At Risk:
107
Other Number Affected:
106
Other Number At Risk:
107
Study:
NCT00833833
Results Section:
NCT00833833
Adverse Events Module:
NCT00833833