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 @ 10:46 PM
Ignite Modification Date:
2025-12-26 @ 10:46 PM
NCT ID:
NCT04026412
Group ID:
EG002
Title:
Arm C: CCRT/Durva
Description:
Participants with Previously Untreated, Locally Advanced Non-small Cell Lung Cancer (LA NSCLC) received CCRT Q3W for up to 3 cycles (each cycle is of 21 days) followed by recovery of 42 days followed by intravenous infusion of Durvalumab 10 mg/kg Q2W for up to 1 year.
Deaths Number Affected:
132
Deaths Number At Risk:
None
Serious Number Affected:
145
Serious Number At Risk:
317
Other Number Affected:
307
Other Number At Risk:
317
Study:
NCT04026412
Results Section:
NCT04026412
Adverse Events Module:
NCT04026412