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 @ 3:40 PM
Ignite Modification Date:
2025-12-25 @ 1:50 PM
NCT ID:
NCT03672292
Group ID:
EG000
Title:
SCY-078 Plus Voriconazole
Description:
Either IV voriconazole (loading dose of 6 mg/kg BID on Day 1 followed by maintenance dose of 4 mg/kg BID from Day 2 onwards) OR oral voriconazole (loading dose of 400 mg BID on Day 1 followed by maintenance dose of 200 mg BID from Day 2 onwards).
PLUS Oral SCY-078 tablets (loading dose of 500 mg BID on Days 1 and 2 followed by maintenance dose of 500 mg QD from Day 3 onwards). Treatment duration = minimum 6 weeks/Max 13 weeks
SCY-078: Oral tablets of SCY-078
Voriconazole: Voriconazole IV vials or oral tablets
Deaths Number Affected:
3
Deaths Number At Risk:
None
Serious Number Affected:
6
Serious Number At Risk:
10
Other Number Affected:
10
Other Number At Risk:
10
Study:
NCT03672292
Results Section:
NCT03672292
Adverse Events Module:
NCT03672292