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 @ 11:18 PM
Ignite Modification Date:
2025-12-25 @ 8:58 PM
NCT ID:
NCT01896856
Group ID:
EG004
Title:
Phase 2: Arm A SGI-110 + Irinotecan
Description:
SGI-110 45 mg/m\^2 was administered as a subcutaneous injection on days 1-5 of each 28-day cycle. Irinotecan 125 mg/m\^2 was administered IV on days 8 and 15 of each 28-day cycle.
Growth factor support (filgrastim and peg-filgrastim) was given during cycle 1 with option to give additional growth factor support at subsequent cycles per clinician judgement.
Deaths Number Affected:
3
Deaths Number At Risk:
None
Serious Number Affected:
15
Serious Number At Risk:
62
Other Number Affected:
58
Other Number At Risk:
62
Study:
NCT01896856
Results Section:
NCT01896856
Adverse Events Module:
NCT01896856