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 @ 2:19 AM
Ignite Modification Date:
2025-12-26 @ 12:50 AM
NCT ID:
NCT02972034
Group ID:
EG008
Title:
Arm B: MK-8353 300 mg + Pembrolizumab
Description:
Participants received MK-8353 PO 300 mg once each day (QD) on Days 1 through 21 of each 21-day cycle PLUS pembrolizumab 200 mg IV on Day 1 of each 21-day cycle for up to 35 cycles.
Deaths Number Affected:
8
Deaths Number At Risk:
None
Serious Number Affected:
3
Serious Number At Risk:
10
Other Number Affected:
10
Other Number At Risk:
10
Study:
NCT02972034
Results Section:
NCT02972034
Adverse Events Module:
NCT02972034