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:
2025-12-26 @ 11:11 PM
Ignite Modification Date:
2025-12-26 @ 11:11 PM
NCT ID:
NCT03095612
Group ID:
EG003
Title:
Dose Expansion: Selinexor 60 mg + Docetaxel 75mg/m2
Description:
Selinexor dose escalation: 60mg once weekly. Docetaxel 75 mg/m2 IV, 60 every 3 weeks.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
33
Other Number Affected:
33
Other Number At Risk:
33
Study:
NCT03095612
Results Section:
NCT03095612
Adverse Events Module:
NCT03095612