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 @ 8:02 PM
Ignite Modification Date:
2025-12-25 @ 5:35 PM
NCT ID:
NCT04199104
Group ID:
EG000
Title:
Pembrolizumab + Lenvatinib First Course
Description:
Participants were administered Pembrolizumab 200mg by intravenous IV infusion on Day 1 of each 21-day cycle (Q3W) plus Lenvatinib 20 mg orally once a day (QD).
Deaths Number Affected:
152
Deaths Number At Risk:
None
Serious Number Affected:
152
Serious Number At Risk:
254
Other Number Affected:
244
Other Number At Risk:
254
Study:
NCT04199104
Results Section:
NCT04199104
Adverse Events Module:
NCT04199104