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:
2025-12-25 @ 2:45 AM
Ignite Modification Date:
2025-12-26 @ 1:25 AM
NCT ID:
NCT03852433
Group ID:
EG001
Title:
Bulevirtide 2 mg/Day + PEG-IFN Alfa
Description:
Participants received bulevirtide 2 mg once a day in combination with PEG-IFN alfa 180 mcg once a week for 48 weeks followed by bulevirtide 2 mg once a day for 48 weeks.
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
3
Serious Number At Risk:
50
Other Number Affected:
49
Other Number At Risk:
50
Study:
NCT03852433
Results Section:
NCT03852433
Adverse Events Module:
NCT03852433