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 @ 12:18 PM
Ignite Modification Date:
2025-12-25 @ 12:02 PM
NCT ID:
NCT04418661
Group ID:
EG001
Title:
Part 1- SAR442720 200mg BIW + Pembrolizumab
Description:
Participants were administered SAR442720 200 mg orally BIW on Days 1 and 2 along with pembrolizumab 200 mg via IV infusion Q3W in 21-day cycles until disease progression, unacceptable AEs, or the participant's or investigator's decision to stop the treatment.
Deaths Number Affected:
6
Deaths Number At Risk:
None
Serious Number Affected:
7
Serious Number At Risk:
13
Other Number Affected:
13
Other Number At Risk:
13
Study:
NCT04418661
Results Section:
NCT04418661
Adverse Events Module:
NCT04418661