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 @ 7:40 PM
Ignite Modification Date:
2025-12-25 @ 5:19 PM
NCT ID:
NCT01115803
Group ID:
EG006
Title:
Arm B - 50 mg LY2584702 BID + 10 mg Everolimus QD
Description:
50 mg LY2584702 administered orally BID plus 150 mg everolimus administered orally QD for 2 28-day cycles.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
2
Serious Number At Risk:
6
Other Number Affected:
6
Other Number At Risk:
6
Study:
NCT01115803
Results Section:
NCT01115803
Adverse Events Module:
NCT01115803