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 @ 3:16 PM
Ignite Modification Date:
2025-12-25 @ 1:37 PM
NCT ID:
NCT03524092
Group ID:
EG000
Title:
Maintenance Period: Miri IR - PBO SC
Description:
Participants who were responders to blinded mirikizumab (miri) at Week 12 in induction study (LUCENT-1) randomized to withdraw from mirikizumab and start receiving PBO SC every 4 weeks (Q4W) from Week 0 of maintenance study (LUCENT-2) until Week 40 or until loss of response was confirmed.
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
15
Serious Number At Risk:
192
Other Number Affected:
57
Other Number At Risk:
192
Study:
NCT03524092
Results Section:
NCT03524092
Adverse Events Module:
NCT03524092