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 @ 5:39 PM
Ignite Modification Date:
2025-12-25 @ 3:09 PM
NCT ID:
NCT03068468
Group ID:
EG002
Title:
BIIB092 Late Start (Open-label Extension Period)
Description:
Late start participants received only placebo in the placebo-controlled period and assigned to BIIB092 2000 mg IV infusion once every 4 weeks starting at Week 52 in the OLE period.
Deaths Number Affected:
10
Deaths Number At Risk:
None
Serious Number Affected:
40
Serious Number At Risk:
137
Other Number Affected:
69
Other Number At Risk:
137
Study:
NCT03068468
Results Section:
NCT03068468
Adverse Events Module:
NCT03068468