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 @ 3:57 PM
Ignite Modification Date:
2025-12-25 @ 2:00 PM
NCT ID:
NCT01316692
Group ID:
EG000
Title:
MLN8237
Description:
Patients receive oral Aurora A kinase inhibitor MLN8237 every 12 hours on days 1-7. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.
laboratory biomarker identification and analysis: Correlative studies
biopsy: Correlative studies
immunohistochemistry/tissue microarrays: Correlative studies
TdT-mediated dUTP nick end labeling assay: Correlative studies
mass spectrometry: Correlative studies
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
2
Serious Number At Risk:
15
Other Number Affected:
12
Other Number At Risk:
12
Study:
NCT01316692
Results Section:
NCT01316692
Adverse Events Module:
NCT01316692