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 @ 9:45 PM
Ignite Modification Date:
2025-12-25 @ 7:25 PM
NCT ID:
NCT03930732
Group ID:
EG000
Title:
Placebo
Description:
Participants received placebo matched to dupilumab 300 mg as SC injections q2w up to a maximum of 52 weeks (last dose administered at Week 50, EOT visit occurred 2 weeks after last administration of treatment i.e., at Week 52).
Deaths Number Affected:
9
Deaths Number At Risk:
None
Serious Number Affected:
74
Serious Number At Risk:
470
Other Number Affected:
172
Other Number At Risk:
470
Study:
NCT03930732
Results Section:
NCT03930732
Adverse Events Module:
NCT03930732