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 @ 2:12 AM
Ignite Modification Date:
2025-12-26 @ 12:40 AM
NCT ID:
NCT03432260
Group ID:
EG001
Title:
Moderate AH DUR-928 90 mg
Description:
Part A (Moderate AH) Middle dose of doses investigated: 30 mg, 90 mg, 150 mg
DUR-928: Dose escalation including 2 doses: 30mg and 90 mg (150 mg did not enroll)
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
3
Other Number Affected:
2
Other Number At Risk:
3
Study:
NCT03432260
Results Section:
NCT03432260
Adverse Events Module:
NCT03432260