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 @ 4:08 PM
Ignite Modification Date:
2025-12-25 @ 2:08 PM
NCT ID:
NCT04049266
Group ID:
EG000
Title:
KSI-301 5 mg Q12W-Q20W
Description:
Participants randomized to this arm received 5 milligrams (mg) KSI-301 intravitreal (IVT) injections once every 4 weeks (Q4W) to Week 8, followed by 5 mg KSI-301 IVT injections based on disease activity assessments and may vary from Q12W to Q20W until Week 52.
Deaths Number Affected:
4
Deaths Number At Risk:
None
Serious Number Affected:
35
Serious Number At Risk:
277
Other Number Affected:
82
Other Number At Risk:
277
Study:
NCT04049266
Results Section:
NCT04049266
Adverse Events Module:
NCT04049266