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 @ 1:04 PM
Ignite Modification Date:
2025-12-25 @ 12:20 PM
NCT ID:
NCT01784861
Group ID:
EG004
Title:
Phase I Dose Level 4: X-82 + Everolimus
Description:
* Everolimus 10mg by mouth once daily for each cycle MUST BE TAKEN FIRST
* X-82 400 mg by mouth once daily 2 HOURS AFTER everolimus dose
* 28 days =1 cycle
X-82
Everolimus
Deaths Number Affected:
2
Deaths Number At Risk:
None
Serious Number Affected:
2
Serious Number At Risk:
3
Other Number Affected:
3
Other Number At Risk:
3
Study:
NCT01784861
Results Section:
NCT01784861
Adverse Events Module:
NCT01784861