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 @ 10:42 PM
Ignite Modification Date:
2025-12-25 @ 8:13 PM
NCT ID:
NCT03818035
Group ID:
EG003
Title:
Group 2c: Guselkumab 100 mg Q8W
Description:
Non-super responders (PASI score greater than \[\>\] 0 at Week 20 and/or Week 28) who completed study Part 1 continued to receive guselkumab 100 mg SC injection Q8W dosing regimen starting at Week 28 till Week 60. Participants were followed from Week 28 till Week 68 or early termination prior to Week 68.
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
33
Serious Number At Risk:
525
Other Number Affected:
367
Other Number At Risk:
525
Study:
NCT03818035
Results Section:
NCT03818035
Adverse Events Module:
NCT03818035