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 @ 7:34 PM
Ignite Modification Date:
2025-12-25 @ 5:15 PM
NCT ID:
NCT03940703
Group ID:
EG000
Title:
Tepotinib and Osimertinib
Description:
Participants received a single oral dose of Tepotinib 500 milligrams (mg) followed by Omisertinib 80 mg once daily until disease progression, death, adverse event leading to discontinuation, study withdrawal or consent withdrawal.
Deaths Number Affected:
59
Deaths Number At Risk:
None
Serious Number Affected:
49
Serious Number At Risk:
128
Other Number Affected:
123
Other Number At Risk:
128
Study:
NCT03940703
Results Section:
NCT03940703
Adverse Events Module:
NCT03940703