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 @ 1:39 AM
Ignite Modification Date:
2025-12-25 @ 11:55 PM
NCT ID:
NCT03397394
Group ID:
EG000
Title:
HRD Unknown
Description:
Patients with HRD status unknown who received continuous dosing with rucaparib 600 mg twice a day (BID) in 28-day cycles. Patients whose tumor genome-wide LOH was not tested or not determined were considered HRD unknown.
Deaths Number Affected:
9
Deaths Number At Risk:
None
Serious Number Affected:
20
Serious Number At Risk:
47
Other Number Affected:
45
Other Number At Risk:
47
Study:
NCT03397394
Results Section:
NCT03397394
Adverse Events Module:
NCT03397394