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:
2025-12-26 @ 12:15 PM
Ignite Modification Date:
2025-12-26 @ 12:15 PM
NCT ID:
NCT04145700
Group ID:
EG000
Title:
Ramucirumab + Gemcitabine + Docetaxel
Description:
Participants received intravenous infusions of ramucirumab 9 mg/kg, gemcitabine 900 mg/m2 on days 1, 8, and docetaxel 75 mg/m2 on day 8 of a 21-day cycle until disease progression or a criterion for discontinuation were met.
Deaths Number Affected:
8
Deaths Number At Risk:
None
Serious Number Affected:
8
Serious Number At Risk:
16
Other Number Affected:
15
Other Number At Risk:
16
Study:
NCT04145700
Results Section:
NCT04145700
Adverse Events Module:
NCT04145700