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 @ 3:50 PM
Ignite Modification Date:
2025-12-25 @ 1:56 PM
NCT ID:
NCT03059992
Group ID:
EG000
Title:
Ibrexafungerp (SCY-078)
Description:
Ibrexafungerp (SCY-078), orally administered QD for up to 180 days.
Ibrexafungerp: Experimental Study Drug
Deaths Number Affected:
15
Deaths Number At Risk:
None
Serious Number Affected:
102
Serious Number At Risk:
233
Other Number Affected:
215
Other Number At Risk:
233
Study:
NCT03059992
Results Section:
NCT03059992
Adverse Events Module:
NCT03059992