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 @ 1:11 AM
Ignite Modification Date:
2025-12-25 @ 11:22 PM
NCT ID:
NCT02019693
Group ID:
EG000
Title:
Capmatinib (INC280)
Description:
Participants received a starting dose of 600mg twice a day (BID) of capmatinib initially; following a change in formulation during the study, the starting dose was changed to 400mg BID, based on pharmacokinetic (PK) studies that demonstrated that this corresponded to the starting dose of 600mg BID of the old formulation.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
6
Serious Number At Risk:
20
Other Number Affected:
20
Other Number At Risk:
20
Study:
NCT02019693
Results Section:
NCT02019693
Adverse Events Module:
NCT02019693