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:
EG002
Title:
Cohort B: Pembrolizumab First Course
Description:
Participants in Cohort B previously received no prior systemic treatment for metastatic breast cancer AND had a programmed cell death-ligand 1 (PD-L1) positive tumor expression. Participants were administered pembrolizumab 200 mg IV on Day 1 of each 3-week cycle (Q3W) for up to 35 cycles (up to \~2 years).
Deaths Number Affected:
63
Deaths Number At Risk:
None
Serious Number Affected:
19
Serious Number At Risk:
84
Other Number Affected:
79
Other Number At Risk:
84
Study:
NCT02447003
Results Section:
NCT02447003
Adverse Events Module:
NCT02447003