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 @ 1:39 AM
Ignite Modification Date:
2025-12-25 @ 11:54 PM
NCT ID:
NCT04732494
Group ID:
EG001
Title:
Arm B: Tislelizumab Plus Placebo
Description:
Participants received 200 mg tislelizumab plus placebo intravenously once every 3 weeks until disease progression, unacceptable toxicity, or withdrawal of informed consent, whichever occurred first.
Deaths Number Affected:
36
Deaths Number At Risk:
None
Serious Number Affected:
28
Serious Number At Risk:
63
Other Number Affected:
54
Other Number At Risk:
63
Study:
NCT04732494
Results Section:
NCT04732494
Adverse Events Module:
NCT04732494