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 @ 5:35 PM
Ignite Modification Date:
2025-12-25 @ 3:06 PM
NCT ID:
NCT02539368
Group ID:
EG002
Title:
Switched From Remicade to CT-P13
Description:
Participants diagnosed with either CD or UC and who were previously treated with Remicade continuously as per usual clinical practice of IBD, switched to CT-P13 once, either at enrollment or during the study were observed for a duration of approximately 24 months.
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
57
Serious Number At Risk:
358
Other Number Affected:
90
Other Number At Risk:
358
Study:
NCT02539368
Results Section:
NCT02539368
Adverse Events Module:
NCT02539368