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 @ 7:37 PM
Ignite Modification Date:
2025-12-25 @ 5:18 PM
NCT ID:
NCT03149003
Group ID:
EG001
Title:
Part 2 - Arm 1: DSP-7888 Dosing Emulsion Plus Bevacizumab
Description:
DSP-7888 Dosing Emulsion: DSP-7888 Dosing Emulsion will be administered i.d. every 7 ± 1 day for Doses 1 to 5, every 14 ± 3 days for Doses 6 to 15, and every 28 ± 7 days for Doses 16 and above.
Bevacizumab: Bevacizumab will be administered intravenously every 14 ± 3 days at 10 mg/kg.
Deaths Number Affected:
96
Deaths Number At Risk:
None
Serious Number Affected:
10
Serious Number At Risk:
108
Other Number Affected:
106
Other Number At Risk:
108
Study:
NCT03149003
Results Section:
NCT03149003
Adverse Events Module:
NCT03149003