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 @ 7:15 PM
Ignite Modification Date:
2025-12-25 @ 4:53 PM
NCT ID:
NCT03019003
Group ID:
EG001
Title:
Low Dose 5'Aza (40 mg/m^2) for Days 1-5 and 8-12 + Durvalumab 1500 mg Q4W + Tremelimumab 75 mg Q4W
Description:
Low dose 5'aza (40 mg/m\^2) administered subcutaneously daily for 10 days + Durvalumab + Tremelimumab
Deaths Number Affected:
4
Deaths Number At Risk:
None
Serious Number Affected:
4
Serious Number At Risk:
5
Other Number Affected:
2
Other Number At Risk:
5
Study:
NCT03019003
Results Section:
NCT03019003
Adverse Events Module:
NCT03019003