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 @ 11:40 PM
Ignite Modification Date:
2025-12-25 @ 9:30 PM
NCT ID:
NCT02588651
Group ID:
EG000
Title:
Brentuximab Vedotin
Description:
Brentuximab vedotin 1.8 mg/kg intravenously (IV) once every 3 weeks
Brentuximab vedotin: study drug given intravenously to determine efficacy in study diseases
Deaths Number Affected:
17
Deaths Number At Risk:
None
Serious Number Affected:
10
Serious Number At Risk:
23
Other Number Affected:
23
Other Number At Risk:
23
Study:
NCT02588651
Results Section:
NCT02588651
Adverse Events Module:
NCT02588651