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 @ 4:07 PM
Ignite Modification Date:
2025-12-25 @ 2:08 PM
NCT ID:
NCT03596866
Group ID:
EG000
Title:
Brigatinib
Description:
Participants were administered brigatinib 90 mg, tablets, orally, QD for 7 days, followed by brigatinib 180 mg, tablets, orally, QD until objective disease progression per RECIST v1.1, as assessed by the investigator, or intolerable toxicity, or up to 63.47 months.
Deaths Number Affected:
37
Deaths Number At Risk:
None
Serious Number Affected:
38
Serious Number At Risk:
125
Other Number Affected:
122
Other Number At Risk:
125
Study:
NCT03596866
Results Section:
NCT03596866
Adverse Events Module:
NCT03596866