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 @ 5:23 PM
Ignite Modification Date:
2025-12-25 @ 2:58 PM
NCT ID:
NCT00676650
Group ID:
EG000
Title:
Sunitinib and Prednisone
Description:
Sunitinib capsules administered orally as a continuous daily dose in a continuous regimen, expressed as 4-week cycles; starting dose of 37.5 milligrams (mg) with option to increase dose to 50 mg at Cycle 3. Prednisone administered continuously at 5 mg orally twice a day (BID) as either a tablet, solution or concentrated solution.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
275
Serious Number At Risk:
581
Other Number Affected:
573
Other Number At Risk:
581
Study:
NCT00676650
Results Section:
NCT00676650
Adverse Events Module:
NCT00676650