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 @ 10:19 PM
Ignite Modification Date:
2025-12-25 @ 7:52 PM
NCT ID:
NCT03875235
Group ID:
EG001
Title:
Placebo + Gemcitabine + Cisplatin
Description:
Drug: Placebo IV infusion every 3 weeks with gemcitabine plus cisplatin up to 8 cycles followed by monotherapy every 4 weeks until disease progression or other discontinuation criteria.
Deaths Number Affected:
226
Deaths Number At Risk:
None
Serious Number Affected:
149
Serious Number At Risk:
342
Other Number Affected:
330
Other Number At Risk:
342
Study:
NCT03875235
Results Section:
NCT03875235
Adverse Events Module:
NCT03875235