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 @ 3:26 PM
Ignite Modification Date:
2025-12-25 @ 1:43 PM
NCT ID:
NCT02641392
Group ID:
EG002
Title:
GED-0301 160 mg 4 Weeks Alt
Description:
Participants received one of three dose regimens up to week 208:
1\) alternating placebo daily for 4 weeks and GED-0301 160 mg daily for 4 weeks or (2) alternating GED-0301 160 mg daily for 4 weeks and placebo daily for 4 weeks or (3) GED-0301 160 mg daily for 12 weeks, followed by alternating placebo daily for 4 weeks and GED-0301 160 mg daily for 4 weeks
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
41
Serious Number At Risk:
293
Other Number Affected:
92
Other Number At Risk:
293
Study:
NCT02641392
Results Section:
NCT02641392
Adverse Events Module:
NCT02641392