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 @ 12:47 PM
Ignite Modification Date:
2025-12-25 @ 12:15 PM
NCT ID:
NCT01606761
Group ID:
EG003
Title:
W24 to W52-Placebo to 100 mg q2w Due to EE or CO
Description:
Participants who received matching placebo in the placebo controlled period and were re-randomized (due to early escape \[EE\] at Week 18 or crossed over \[CO\] at Week 24) to receive subcutaneous (SC) sirukumab 100 mg q4w dose regimen up to Week 52.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
18
Serious Number At Risk:
126
Other Number Affected:
63
Other Number At Risk:
126
Study:
NCT01606761
Results Section:
NCT01606761
Adverse Events Module:
NCT01606761