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 @ 2:43 AM
Ignite Modification Date:
2025-12-26 @ 1:22 AM
NCT ID:
NCT03835533
Group ID:
EG000
Title:
Cohort A: NKTR-214 + Nivolumab
Description:
NKTR-214 (Cohort A): NKTR-214 will be administered intravenously every 3 weeks for up to 2 years
Nivolumab (Cohort A, B and C): Nivolumab will be administered intravenously every 3 weeks for up to 2 years to cohort A, every 4 weeks for up to 2 years for cohort B and C.
Deaths Number Affected:
5
Deaths Number At Risk:
None
Serious Number Affected:
7
Serious Number At Risk:
14
Other Number Affected:
13
Other Number At Risk:
14
Study:
NCT03835533
Results Section:
NCT03835533
Adverse Events Module:
NCT03835533