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 @ 12:23 AM
Ignite Modification Date:
2025-12-25 @ 10:28 PM
NCT ID:
NCT03428958
Group ID:
EG006
Title:
NUC-3373 + Irinotecan Weekly (PK Sub-study)
Description:
Arm 2b (PK sub-study): NUC-3373+LV (400 mg/m2) administered weekly on Days 1, 8, 15 and 22 of 28-day cycles in combination with irinotecan (180 mg/m2) on Days 1 and 15.
NUFIRI: NUC-3373 + irinotecan
Deaths Number Affected:
6
Deaths Number At Risk:
None
Serious Number Affected:
2
Serious Number At Risk:
8
Other Number Affected:
8
Other Number At Risk:
8
Study:
NCT03428958
Results Section:
NCT03428958
Adverse Events Module:
NCT03428958