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 @ 11:51 PM
Ignite Modification Date:
2025-12-25 @ 9:46 PM
NCT ID:
NCT03451851
Group ID:
EG001
Title:
PCP-Group 2 (Part 1): Guselkumab (Week 0-16)
Description:
Adolescent participants received weight-adjusted doses of guselkumab (1.3 mg/kg for body weight \[BW\] \<70 kg, 100 mg for BW \>=70 kg) via subcutaneous injection at Weeks 0, 4, and 12 during PCP. Once adolescent participants completed Week 16, eligible participants aged \>=6 to \<12 years began receiving the same dose regimen starting from Week 0 until Week 16.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
1
Serious Number At Risk:
41
Other Number Affected:
17
Other Number At Risk:
41
Study:
NCT03451851
Results Section:
NCT03451851
Adverse Events Module:
NCT03451851