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 @ 12:24 PM
Ignite Modification Date:
2025-12-25 @ 12:04 PM
NCT ID:
NCT02606461
Group ID:
EG004
Title:
Phase 2 Open-label: Selinexor
Description:
Participants in the placebo group who had PD during Phase 2 double-blinded treatment were entered in open-label and received selinexor 60 mg tablet twice-weekly during Weeks 1 to 6 of each 6-week (42-day) cycle.
Deaths Number Affected:
20
Deaths Number At Risk:
None
Serious Number Affected:
13
Serious Number At Risk:
24
Other Number Affected:
24
Other Number At Risk:
24
Study:
NCT02606461
Results Section:
NCT02606461
Adverse Events Module:
NCT02606461