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 @ 9:44 PM
Ignite Modification Date:
2025-12-25 @ 7:25 PM
NCT ID:
NCT04311632
Group ID:
EG001
Title:
Arm 2
Description:
TCD601 (0.6mg/kg) administered with the standard of care (SoC) consisting of concentration-controlled tacrolimus (TAC) combined with mycophenolate mofetil (MMF) and corticosteroids (CS).
TCD601: Investigational Product
Tacrolimus (TAC): Standard of Care Concomitant Immunosuppression
Corticosteroids (CS): Standard of Care Concomitant Immunosuppression
Mycophenolate Mofetil (MMF): Standard of Care Concomitant Immunosuppression
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
1
Serious Number At Risk:
4
Other Number Affected:
4
Other Number At Risk:
4
Study:
NCT04311632
Results Section:
NCT04311632
Adverse Events Module:
NCT04311632