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 @ 11:38 PM
Ignite Modification Date:
2025-12-25 @ 9:29 PM
NCT ID:
NCT01118351
Group ID:
EG000
Title:
Arm I
Description:
Patients receive oral sunitinib malate once daily on days 1-28. Treatment repeats every 28 days for 3 courses in the absence of disease progression or unacceptable toxicity.
sunitinib malate: Given orally
immunohistochemistry staining method: Correlative studies
TdT-mediated dUTP nick end labeling assay: Correlative studies
light microscopy: Correlative studies
laboratory biomarker analysis: Correlative studies
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
3
Serious Number At Risk:
19
Other Number Affected:
19
Other Number At Risk:
19
Study:
NCT01118351
Results Section:
NCT01118351
Adverse Events Module:
NCT01118351