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:
2025-12-25 @ 2:40 AM
Ignite Modification Date:
2025-12-26 @ 1:18 AM
NCT ID:
NCT01997333
Group ID:
EG001
Title:
CDX-011
Description:
CDX-011 administered on Day 1 of each 21 day cycle until disease progression, discontinuation due to toxicity, withdrawal of consent, or end of study.
Deaths Number Affected:
134
Deaths Number At Risk:
None
Serious Number Affected:
71
Serious Number At Risk:
213
Other Number Affected:
211
Other Number At Risk:
213
Study:
NCT01997333
Results Section:
NCT01997333
Adverse Events Module:
NCT01997333