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 @ 12:22 AM
Ignite Modification Date:
2025-12-25 @ 10:26 PM
NCT ID:
NCT05064358
Group ID:
EG002
Title:
Arm C: Belantamab Mafodotin 2.5 mg/kg Every 6 Weeks (Q6W)
Description:
Participants with RRMM received belantamab mafodotin as 2.5 mg/kg dose on Day 1 of every 6 weeks (Q6W) as a 30-60 minute IV infusion until confirmed disease progression, unacceptable toxicity or death.
Deaths Number Affected:
25
Deaths Number At Risk:
None
Serious Number Affected:
21
Serious Number At Risk:
39
Other Number Affected:
36
Other Number At Risk:
39
Study:
NCT05064358
Results Section:
NCT05064358
Adverse Events Module:
NCT05064358