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 @ 4:41 PM
Ignite Modification Date:
2025-12-25 @ 2:30 PM
NCT ID:
NCT05288166
Group ID:
EG001
Title:
Placebo
Description:
Participants received placebo BID in combination with standard doses of 1000 mg abiraterone once daily and 5 mg prednisone BID administered orally on a continuous dosing schedule on days 1 through 28 of a 28-day cycle until radiographic and/or symptomatic progression or until another discontinuation criterion is met.
Deaths Number Affected:
32
Deaths Number At Risk:
None
Serious Number Affected:
68
Serious Number At Risk:
460
Other Number Affected:
380
Other Number At Risk:
460
Study:
NCT05288166
Results Section:
NCT05288166
Adverse Events Module:
NCT05288166