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 @ 10:31 PM
Ignite Modification Date:
2025-12-25 @ 8:04 PM
NCT ID:
NCT01695135
Group ID:
EG002
Title:
Placebo + Prednisone (DB) to AA + Prednisone (Open-label)
Description:
Participants with disease progression during the double-blind treatment phase received abiraterone acetate 1000 mg once daily + prednisone 5 mg twice daily in open-label extension treatment phase based on the participant's choice and treating physician's decision if they met the criteria for subsequent abiraterone acetate treatment until they no longer derive clinical benefit, unacceptable toxicity, initiation of a subsequent anticancer therapy, or serious protocol violation.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
25
Serious Number At Risk:
49
Other Number Affected:
35
Other Number At Risk:
49
Study:
NCT01695135
Results Section:
NCT01695135
Adverse Events Module:
NCT01695135