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 @ 5:13 PM
Ignite Modification Date:
2025-12-25 @ 2:51 PM
NCT ID:
NCT01981850
Group ID:
EG006
Title:
Main Phase Stage 2: RO7490677 10 mg/kg IV Q4W
Description:
Participants were treated with single agent PRM-151 at a dose of 10 mg/kg administered as a 60 minute IV infusion on Days 1, 3, and 5 of Cycle 1 and Day 1 of each subsequent 28 day cycle for nine cycles.
Deaths Number Affected:
9
Deaths Number At Risk:
None
Serious Number Affected:
14
Serious Number At Risk:
32
Other Number Affected:
31
Other Number At Risk:
32
Study:
NCT01981850
Results Section:
NCT01981850
Adverse Events Module:
NCT01981850