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 @ 7:16 PM
Ignite Modification Date:
2025-12-25 @ 4:53 PM
NCT ID:
NCT03206203
Group ID:
EG000
Title:
Arm 1 (Atezolizumab, Carboplatin)
Description:
Patients receive atezolizumab IV over 30-60 minutes and carboplatin IV on day 1. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.
Atezolizumab: Given by vein
Carboplatin: Given by vein
Laboratory Biomarker: Correlative study
Quality-of-Life Assessment: Ancillary studies
Deaths Number Affected:
38
Deaths Number At Risk:
None
Serious Number Affected:
23
Serious Number At Risk:
56
Other Number Affected:
54
Other Number At Risk:
56
Study:
NCT03206203
Results Section:
NCT03206203
Adverse Events Module:
NCT03206203