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 @ 10:44 PM
Ignite Modification Date:
2025-12-25 @ 8:14 PM
NCT ID:
NCT02607735
Group ID:
EG002
Title:
SOF/VEL/VOX (Deferred Treatment Substudy)
Description:
Participants who completed placebo treatment were eligible for open-label Deferred Treatment Substudy.
SOF/VEL/VOX (400/100/100 mg) FDC tablet orally once daily with food for 12 weeks
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
6
Serious Number At Risk:
147
Other Number Affected:
87
Other Number At Risk:
147
Study:
NCT02607735
Results Section:
NCT02607735
Adverse Events Module:
NCT02607735