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 @ 7:12 PM
Ignite Modification Date:
2025-12-25 @ 4:47 PM
NCT ID:
NCT02803203
Group ID:
EG000
Title:
Osimertinib and Bevacizumab
Description:
Phases 1+2: Osimertinib + Bevacizumab 80 mg Osimertinib PO QD and 15 mg/kg Bevacizumab IV Q3W
This section accurately reflects the flow of participants as all participants were enrolled into the same dosing cohort.
Deaths Number Affected:
37
Deaths Number At Risk:
None
Serious Number Affected:
26
Serious Number At Risk:
49
Other Number Affected:
49
Other Number At Risk:
49
Study:
NCT02803203
Results Section:
NCT02803203
Adverse Events Module:
NCT02803203