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 @ 1:18 AM
Ignite Modification Date:
2025-12-25 @ 11:27 PM
NCT ID:
NCT01753193
Group ID:
EG000
Title:
Anifrolumab
Description:
Participants received intravenous (IV) infusion of anifrolumab (MEDI-546) 1000 milligrams (mg) every 4 weeks (Q4W) from Day 1 (Week 0) until 12-Feb-2015 (approval of protocol amendment 4); and thereafter received 300 mg Q4W for up to 3 years or until the sponsor discontinued development of anifrolumab, whichever came first.
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
50
Serious Number At Risk:
218
Other Number Affected:
164
Other Number At Risk:
218
Study:
NCT01753193
Results Section:
NCT01753193
Adverse Events Module:
NCT01753193