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 @ 12:31 PM
Ignite Modification Date:
2025-12-25 @ 12:09 PM
NCT ID:
NCT01010061
Group ID:
EG001
Title:
Chlorambucil (Clb)
Description:
Participants received chlorambucil 0.5 mg/kg orally on Day 1 and 15 of each 28-day cycle (6 Cycles). Participants with Progressive Disease or within 6 months of follow-up were allowed to cross over to receive obinutuzumab + chlorambucil.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
45
Serious Number At Risk:
116
Other Number Affected:
89
Other Number At Risk:
116
Study:
NCT01010061
Results Section:
NCT01010061
Adverse Events Module:
NCT01010061