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 @ 5:00 AM
Ignite Modification Date:
2025-12-26 @ 4:00 AM
NCT ID:
NCT04163718
Group ID:
EG000
Title:
Treatment With Umbralisib
Description:
Umbralisib: 800 mg Umbralisib will be self-administered on an outpatient basis. Umbralisib will be taken orally once daily within 30 minutes of a meal until removal from study. This treatment will be administered in 4 week (28-day) cycles.
Deaths Number Affected:
2
Deaths Number At Risk:
None
Serious Number Affected:
10
Serious Number At Risk:
12
Other Number Affected:
12
Other Number At Risk:
12
Study:
NCT04163718
Results Section:
NCT04163718
Adverse Events Module:
NCT04163718