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 @ 3:59 PM
Ignite Modification Date:
2025-12-25 @ 2:02 PM
NCT ID:
NCT02595892
Group ID:
EG002
Title:
Arm II (Gemcitabine, ATR Kinase Inhibitor M6620) After Crossover
Description:
Per protocol, participants could cross-over from "Arm I (Gemcitabine Hydrochloride)" to "Arm II (Gemcitabine, ATR Kinase Inhibitor M6620)" if disease progression was experienced. This adverse event arm demonstrates the events which occurred during Arm II treatment for the 15 total participants who crossed over.
Deaths Number Affected:
11
Deaths Number At Risk:
None
Serious Number Affected:
3
Serious Number At Risk:
15
Other Number Affected:
15
Other Number At Risk:
15
Study:
NCT02595892
Results Section:
NCT02595892
Adverse Events Module:
NCT02595892