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 @ 11:50 PM
Ignite Modification Date:
2025-12-25 @ 9:45 PM
NCT ID:
NCT02336451
Group ID:
EG001
Title:
Arm 2 (PrALKi=Y, PrBRad=N)
Description:
Participants with metastases in the brain without evidence of LC, previously untreated with radiation to the brain but with prior exposure to an ALK-I. Previous treatment with ALK-I other than crizotinib was not allowed in this arm 2 as of protocol amendment 3 and had to present with active brain lesion defined as a lesion free of any local treatment (like stereotactic radiosurgery or whole brain radiation).
Deaths Number Affected:
5
Deaths Number At Risk:
None
Serious Number Affected:
17
Serious Number At Risk:
40
Other Number Affected:
40
Other Number At Risk:
40
Study:
NCT02336451
Results Section:
NCT02336451
Adverse Events Module:
NCT02336451