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 @ 3:53 PM
Ignite Modification Date:
2025-12-25 @ 1:58 PM
NCT ID:
NCT02525692
Group ID:
EG003
Title:
Arm D
Description:
Patients with confirmed WHO Grade IV glioma with H3 K27M mutation (any number of recurrences were allowed).
Patients received 625 mg oral ONC201 once weekly (Days 1, 8, and 15 of each cycle).
Deaths Number Affected:
20
Deaths Number At Risk:
None
Serious Number Affected:
11
Serious Number At Risk:
30
Other Number Affected:
29
Other Number At Risk:
30
Study:
NCT02525692
Results Section:
NCT02525692
Adverse Events Module:
NCT02525692