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 @ 4:14 AM
Ignite Modification Date:
2025-12-26 @ 3:14 AM
NCT ID:
NCT03747120
Group ID:
EG002
Title:
Arm C: TH-Pembrolizumab
Description:
Arm C: Paclitaxel weekly x12 + Trastuzumab + Pembrolizumab
All subjects may receive standard of care systemic therapy after surgery per their treating physician's discretion.
Paclitaxel: All subjects will receive Paclitaxel weekly for 12 weeks
Trastuzumab: All subjects will receive Trastuzumab every 3 weeks
Pembrolizumab: Arm B and Arm C subjects will receive Pembrolizumab every 3 weeks
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
1
Serious Number At Risk:
20
Other Number Affected:
11
Other Number At Risk:
20
Study:
NCT03747120
Results Section:
NCT03747120
Adverse Events Module:
NCT03747120