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 @ 5:02 PM
Ignite Modification Date:
2025-12-25 @ 2:42 PM
NCT ID:
NCT00326950
Group ID:
EG000
Title:
E7389
Description:
E7389 will be administered intravenously on Days 1 and 8 of a 21-day cycle. Initial dose level will be 0.7 mg/m\^2, with planned dose levels of 1.0, 1.4, \& 2.0 mg/m\^2.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
5
Serious Number At Risk:
15
Other Number Affected:
15
Other Number At Risk:
15
Study:
NCT00326950
Results Section:
NCT00326950
Adverse Events Module:
NCT00326950