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 @ 3:31 AM
Ignite Modification Date:
2025-12-26 @ 2:13 AM
NCT ID:
NCT00548405
Group ID:
EG003
Title:
Alemtuzumab (Pooled)
Description:
Included all participants who received alemtuzumab 12 mg or 24 mg per day IV infusion on 5 consecutive days at Month 0, followed by alemtuzumab 12 mg or 24 mg per day IV infusion on 3 consecutive days at Month 12.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
115
Serious Number At Risk:
596
Other Number Affected:
586
Other Number At Risk:
596
Study:
NCT00548405
Results Section:
NCT00548405
Adverse Events Module:
NCT00548405