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 @ 11:44 PM
Ignite Modification Date:
2025-12-25 @ 9:37 PM
NCT ID:
NCT01208051
Group ID:
EG003
Title:
Phase II Arm A (Cediranib Maleate)
Description:
Patients receive cediranib maleate 30 mg PO QD on days 1-28. Cycles repeat every 4 weeks in the absence of disease progression or unacceptable toxicity.
Cediranib: Given PO
Cediranib Maleate: Given PO
Laboratory Biomarker Analysis: Correlative studies
Deaths Number Affected:
8
Deaths Number At Risk:
None
Serious Number Affected:
16
Serious Number At Risk:
39
Other Number Affected:
38
Other Number At Risk:
39
Study:
NCT01208051
Results Section:
NCT01208051
Adverse Events Module:
NCT01208051