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 @ 12:33 PM
Ignite Modification Date:
2025-12-25 @ 12:10 PM
NCT ID:
NCT03277261
Group ID:
EG000
Title:
Ublituximab + Oral Placebo
Description:
Participants were administered ublituximab 150 mg, IV infusion over 4 h on Day 1 followed by 450 mg over 1 h on Days 15, 168, 336 and 504 (Week 72) along with the oral placebo QD from Day 1 up to the last day of Week 95.
Deaths Number Affected:
2
Deaths Number At Risk:
None
Serious Number Affected:
31
Serious Number At Risk:
273
Other Number Affected:
197
Other Number At Risk:
273
Study:
NCT03277261
Results Section:
NCT03277261
Adverse Events Module:
NCT03277261