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 @ 11:15 PM
Ignite Modification Date:
2025-12-25 @ 8:52 PM
NCT ID:
NCT03580356
Group ID:
EG012
Title:
Transitioned to Ligelizumab 120mg (Adults)
Description:
Placebo Adults patients who transitioned to ligelizumab 120mg; 1 injection of 1.0mL of ligelizumab, 120 mg + 1 injection of 1.0 mL ligelizumab placebo from Week 24 through Week 48. At week 24 participants received active drug. Safety events from week 24 to end of study are presented.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
90
Other Number Affected:
37
Other Number At Risk:
90
Study:
NCT03580356
Results Section:
NCT03580356
Adverse Events Module:
NCT03580356