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 @ 2:47 AM
Ignite Modification Date:
2025-12-26 @ 1:28 AM
NCT ID:
NCT03219333
Group ID:
EG000
Title:
Enfortumab Vedotin - Cohort 1
Description:
Participants in Cohort 1 had received prior treatment with platinum-containing chemotherapy. Enfortumab vedotin, at a dose of 1.25 mg/kg, was administered to participants as an IV infusion over approximately 30 minutes on Days 1, 8, and 15 of each 28-day cycle.
Deaths Number Affected:
104
Deaths Number At Risk:
None
Serious Number Affected:
59
Serious Number At Risk:
125
Other Number Affected:
123
Other Number At Risk:
125
Study:
NCT03219333
Results Section:
NCT03219333
Adverse Events Module:
NCT03219333