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:
2025-12-25 @ 2:39 AM
Ignite Modification Date:
2025-12-26 @ 1:16 AM
NCT ID:
NCT02592434
Group ID:
EG002
Title:
Placebo
Description:
Participants who completed open-label phase and achieved at least a JIA ACR 30 response in open label phase, were randomized at Week 18 to receive placebo either as oral tablets, (for subjects \>=40 body weight) or oral solution (for subjects \<40 kg body weight), BID, in double-blind phase for additional 26 weeks (up to Week 44).
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
2
Serious Number At Risk:
85
Other Number Affected:
57
Other Number At Risk:
85
Study:
NCT02592434
Results Section:
NCT02592434
Adverse Events Module:
NCT02592434