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 @ 2:30 AM
Ignite Modification Date:
2025-12-26 @ 1:05 AM
NCT ID:
NCT02117934
Group ID:
EG000
Title:
HEPLISAV
Description:
0.5 mL HEPLISAV (20 mcg HBsAg and 3000 mcg 1018)
HEPLISAV and/or Placebo: Intramuscular (IM) injections at Week 0, Week 4, plus a placebo (saline) injection at Week 24
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
345
Serious Number At Risk:
5587
Other Number Affected:
1097
Other Number At Risk:
5587
Study:
NCT02117934
Results Section:
NCT02117934
Adverse Events Module:
NCT02117934