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 @ 7:18 PM
Ignite Modification Date:
2025-12-25 @ 4:57 PM
NCT ID:
NCT03770403
Group ID:
EG000
Title:
Efgartigimod
Description:
Participants were administered efgartigimod IV 10 mg/kg over 1 hour every 7 days for 4 administrations per TP for 3 weeks in this study irrespective of whether they received efgartigimod or placebo in ARGX-113-1704. After the fourth infusion, participants entered an ITP of variable duration (minimum 4 weeks between treatment periods). Subsequent TPs were implemented according to clinical response.
Deaths Number Affected:
5
Deaths Number At Risk:
None
Serious Number Affected:
36
Serious Number At Risk:
145
Other Number Affected:
83
Other Number At Risk:
145
Study:
NCT03770403
Results Section:
NCT03770403
Adverse Events Module:
NCT03770403