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 @ 1:23 AM
Ignite Modification Date:
2025-12-25 @ 11:32 PM
NCT ID:
NCT03622593
Group ID:
EG001
Title:
B: Faricimab 6 mg PTI
Description:
Participants randomized to Arm B received 6 milligrams (mg) faricimab intravitreal (IVT) injections Q4W to at least Week 12, followed by a personalized treatment interval (PTI) dosing of 6 mg faricimab IVT injections up to once every 16 weeks (Q16W) through Week 96, followed by the final study visit at Week 100.
Deaths Number Affected:
9
Deaths Number At Risk:
None
Serious Number Affected:
82
Serious Number At Risk:
319
Other Number Affected:
169
Other Number At Risk:
319
Study:
NCT03622593
Results Section:
NCT03622593
Adverse Events Module:
NCT03622593