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:
2025-12-26 @ 4:04 PM
Ignite Modification Date:
2025-12-26 @ 4:04 PM
NCT ID:
NCT02990806
Group ID:
EG002
Title:
Stage 2 and Stage 3: Remicade US to Remicade-US Group
Description:
Participants who received Remicade US during stage 1; were re-randomized during stage 2 to continue Remicade-US dose 3 mg/kg from Week 22 through Week 54 with every 8 weeks dosing intervals. Participants were followed up to Week 62 (Stage 3).
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
28
Serious Number At Risk:
254
Other Number Affected:
80
Other Number At Risk:
254
Study:
NCT02990806
Results Section:
NCT02990806
Adverse Events Module:
NCT02990806