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 @ 1:01 PM
Ignite Modification Date:
2025-12-25 @ 12:19 PM
NCT ID:
NCT02914561
Group ID:
EG006
Title:
Filgotinib 200 mg to Filgotinib 200 mg (Maintenance Study)
Description:
Participants who received filgotinib 200 mg in induction study and who achieved either clinical remission by PRO2 or endoscopic response at Week 10 were re-randomized to the maintenance study and received filgotinib 200 mg and PTM filgotinib 100 mg tablet orally once daily, up to Week 58.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
13
Serious Number At Risk:
118
Other Number Affected:
59
Other Number At Risk:
118
Study:
NCT02914561
Results Section:
NCT02914561
Adverse Events Module:
NCT02914561