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 @ 3:36 PM
Ignite Modification Date:
2025-12-25 @ 1:48 PM
NCT ID:
NCT02864992
Group ID:
EG000
Title:
Part 1 & 2: Cohort A + B + C
Description:
Participants received 500 milligram (mg) of tepotinib once daily in cycles of 21-day duration until disease progression, death, adverse event (AE) leading to discontinuation or withdrawal of consent.
Deaths Number Affected:
200
Deaths Number At Risk:
None
Serious Number Affected:
169
Serious Number At Risk:
337
Other Number Affected:
331
Other Number At Risk:
337
Study:
NCT02864992
Results Section:
NCT02864992
Adverse Events Module:
NCT02864992