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 @ 10:54 PM
Ignite Modification Date:
2025-12-25 @ 8:22 PM
NCT ID:
NCT01109069
Group ID:
EG000
Title:
IBRUTINIB/PCI-32765
Description:
This was a multicenter, open-label, monotherapy, long-term extension study designed to evaluate the long-term (\> 6 months) safety and tolerability of a fixed daily dosing regimen of ibrutinib. PCI-32765: Dose based on parent protocol CLL: chronic lymphocytic leukemia/ SLL: small lymphocytic lymphoma.
Deaths Number Affected:
111
Deaths Number At Risk:
None
Serious Number Affected:
111
Serious Number At Risk:
199
Other Number Affected:
114
Other Number At Risk:
199
Study:
NCT01109069
Results Section:
NCT01109069
Adverse Events Module:
NCT01109069