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 @ 5:05 AM
Ignite Modification Date:
2025-12-26 @ 4:07 AM
NCT ID:
NCT04423718
Group ID:
EG005
Title:
Aflibercept HDq12 (Week 0- 156)
Description:
Participants enrolled in the extension originally assigned to HDq12 in main study and continued with HD aflibercept at their latest dosing interval at Week 96. Participants in this group could have their treatment intervals adjusted in the extension according to pre-specified dose regimen modification (E-DRM) criteria.
Deaths Number Affected:
7
Deaths Number At Risk:
None
Serious Number Affected:
61
Serious Number At Risk:
210
Other Number Affected:
120
Other Number At Risk:
210
Study:
NCT04423718
Results Section:
NCT04423718
Adverse Events Module:
NCT04423718