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:
EG001
Title:
Group 2a: Guselkumab 100 mg Q8W
Description:
Super responders (Psoriasis Area and Severity Index \[PASI\] score = 0 at Week 20 and Week 28) who completed study Part 1, were randomized to receive guselkumab 100 mg SC injection every 8 weeks (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:
0
Deaths Number At Risk:
None
Serious Number Affected:
7
Serious Number At Risk:
148
Other Number Affected:
101
Other Number At Risk:
148
Study:
NCT03818035
Results Section:
NCT03818035
Adverse Events Module:
NCT03818035