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 @ 3:46 AM
Ignite Modification Date:
2025-12-26 @ 2:32 AM
NCT ID:
NCT01754402
Group ID:
EG000
Title:
Cohort 1: 120mg Bendamustine + 3mg Pomalidomide
Description:
* Pomalidomide: once daily oral (PO) dosing on days 1-21, every 28 days
* Bendamustine: once intravenous (IV) dosing on day 1, every 28 days
* Dexamethasone: weekly PO or IV dosing on days 1, 8, 15, and 22 every 28 days
Deaths Number Affected:
6
Deaths Number At Risk:
None
Serious Number Affected:
6
Serious Number At Risk:
6
Other Number Affected:
6
Other Number At Risk:
6
Study:
NCT01754402
Results Section:
NCT01754402
Adverse Events Module:
NCT01754402