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 @ 10:38 PM
Ignite Modification Date:
2025-12-25 @ 8:10 PM
NCT ID:
NCT02432235
Group ID:
EG005
Title:
30 μg/kg
Description:
Participants received an intravenous (IV) infusion of camidanlumab tesirine (30 μg/kg) on Day 1 of each 3-week treatment cycle, for a maximum of 10 cycles.
Camidanlumab tesirine: Intravenous (IV) infusion.
Deaths Number Affected:
3
Deaths Number At Risk:
None
Serious Number Affected:
10
Serious Number At Risk:
20
Other Number Affected:
20
Other Number At Risk:
20
Study:
NCT02432235
Results Section:
NCT02432235
Adverse Events Module:
NCT02432235