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 @ 7:24 PM
Ignite Modification Date:
2025-12-25 @ 5:05 PM
NCT ID:
NCT02447003
Group ID:
EG000
Title:
Cohort A: Pembrolizumab First Course
Description:
Participants in Cohort A previously received at least one prior systemic treatment for metastatic breast cancer. Participants were administered pembrolizumab 200 mg intravenously (IV) on Day 1 of each 3-week cycle (Q3W) for up to 35 cycles (up to \~2 years).
Deaths Number Affected:
154
Deaths Number At Risk:
None
Serious Number Affected:
46
Serious Number At Risk:
170
Other Number Affected:
147
Other Number At Risk:
170
Study:
NCT02447003
Results Section:
NCT02447003
Adverse Events Module:
NCT02447003