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 @ 11:48 AM
Ignite Modification Date:
2025-12-24 @ 11:48 AM
NCT ID:
NCT02125461
Group ID:
EG000
Title:
Durvalumab (MEDI4736)
Description:
Patients in the durvalumab (MEDI4736) monotherapy group were to receive durvalumab 10 mg/kg Q2W via intravenous infusion for up to 12 months.
Deaths Number Affected:
262
Deaths Number At Risk:
None
Serious Number Affected:
138
Serious Number At Risk:
475
Other Number Affected:
436
Other Number At Risk:
475
Study:
NCT02125461
Results Section:
NCT02125461
Adverse Events Module:
NCT02125461