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 @ 1:17 AM
Ignite Modification Date:
2025-12-25 @ 11:26 PM
NCT ID:
NCT03920293
Group ID:
EG000
Title:
Randomized-Controlled Period: Ravulizumab
Description:
Participants received a weight-based single loading dose (2400 to 3000 mg) of ravulizumab IV on Day 1, followed by regular maintenance IV weight-based doses (3000 to 3600 mg) of ravulizumab beginning on Day 15 q8w during the 26-week Randomized-Controlled Period of the study.
Deaths Number Affected:
2
Deaths Number At Risk:
None
Serious Number Affected:
20
Serious Number At Risk:
86
Other Number Affected:
77
Other Number At Risk:
86
Study:
NCT03920293
Results Section:
NCT03920293
Adverse Events Module:
NCT03920293