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 @ 7:51 PM
Ignite Modification Date:
2025-12-25 @ 5:26 PM
NCT ID:
NCT04619004
Group ID:
EG001
Title:
Patritumab Deruxtecan Up-Titration
Description:
Participants with metastatic or locally advanced NSCLC with an EGFR-activating mutation and received a patritumab deruxtecan up-titration regimen
Deaths Number Affected:
28
Deaths Number At Risk:
None
Serious Number Affected:
16
Serious Number At Risk:
50
Other Number Affected:
49
Other Number At Risk:
50
Study:
NCT04619004
Results Section:
NCT04619004
Adverse Events Module:
NCT04619004