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:
2025-12-25 @ 2:08 AM
Ignite Modification Date:
2025-12-26 @ 12:35 AM
NCT ID:
NCT00560560
Group ID:
EG000
Title:
Figitumumab 20 mg/kg
Description:
Figitumumab (CP-751,871) was given in 3-week cycles for a total of up to 17 cycles. Participants can receive treatment beyond 17 cycles provided clinical benefit is being achieved. Figitumumab 20 milligram/kilogram (mg/kg) was administered as an intravenous (IV) infusion on Day 1 and 2 in Cycle 1 (loading dose), and on Day 1 of every cycle thereafter.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
56
Serious Number At Risk:
85
Other Number Affected:
85
Other Number At Risk:
85
Study:
NCT00560560
Results Section:
NCT00560560
Adverse Events Module:
NCT00560560