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 @ 3:19 AM
Ignite Modification Date:
2025-12-26 @ 1:58 AM
NCT ID:
NCT04740905
Group ID:
EG003
Title:
Arm B: Aflibercept Q4W to Faricimab PTI (Part 2)
Description:
In Part 2 (from Week 24 to Week 72), participants received faricimab 6 mg by IVT injection according to a personalized treatment interval (PTI) dosing regimen. To preserve masking for Part 2, a sham procedure was to be administered during study visits at which no faricimab treatment was administered (according to the PTI dosing regimen).
Deaths Number Affected:
2
Deaths Number At Risk:
None
Serious Number Affected:
26
Serious Number At Risk:
267
Other Number Affected:
87
Other Number At Risk:
267
Study:
NCT04740905
Results Section:
NCT04740905
Adverse Events Module:
NCT04740905