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 @ 5:40 PM
Ignite Modification Date:
2025-12-25 @ 3:10 PM
NCT ID:
NCT01253668
Group ID:
EG000
Title:
Arm 1
Description:
Patients receive oral brivanib alaninate daily in the absence of disease progression or unacceptable toxicity.
Brivanib alaninate: Brivanib by mouth daily at a dose of 800mg.
Polymerase chain reaction: Undergo 1241-cG250 PET/CT imaging (correlative studies)
Iodine I 124 chimeric monoclonal antibody G250: Undergo 124I-cG250 PET/CT imaging (correlative studies)
Positron emission tomography/computed tomography: Undergo 1241-cG250 PET/CT imaging (correlative studies)
Protein expression analysis: Correlative studies
Immunohistochemistry: correlative studies
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
0
Other Number Affected:
0
Other Number At Risk:
0
Study:
NCT01253668
Results Section:
NCT01253668
Adverse Events Module:
NCT01253668