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 @ 6:35 PM
Ignite Modification Date:
2025-12-25 @ 4:05 PM
NCT ID:
NCT00788957
Group ID:
EG005
Title:
Part 3: Ganitumab
Description:
Participants randomized to Panitumumab Alone in Part 2 who had disease progression (radiographic or clinical) or intolerability were re-randomized in Part 3 to receive ganitumab 12 mg/kg every 2 weeks until disease progression, intolerability, withdrawal, death, or sponsor decision.
Deaths Number Affected:
8
Deaths Number At Risk:
None
Serious Number Affected:
2
Serious Number At Risk:
11
Other Number Affected:
9
Other Number At Risk:
11
Study:
NCT00788957
Results Section:
NCT00788957
Adverse Events Module:
NCT00788957