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 @ 9:15 PM
Ignite Modification Date:
2025-12-25 @ 7:04 PM
NCT ID:
NCT02853604
Group ID:
EG001
Title:
ADXS11-001
Description:
Participants with HRLACC received ADXS11-001 at a dose of 1x10\^9 CFU by intravenous infusion for approximately 60 minutes every 3 weeks for 3 doses (Weeks 1, 4 and 7) and thereafter, every 8 weeks for 5 doses (Weeks 15, 23, 31, 39, and 47) during treatment phase or until disease recurrence. Participants received a 7-day course of either trimethoprim/sulfamethoxazole or ampicillin starting 72 hours post treatment in prime and maintenance phase.
Deaths Number Affected:
5
Deaths Number At Risk:
None
Serious Number Affected:
10
Serious Number At Risk:
72
Other Number Affected:
62
Other Number At Risk:
72
Study:
NCT02853604
Results Section:
NCT02853604
Adverse Events Module:
NCT02853604