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 @ 4:58 AM
Ignite Modification Date:
2025-12-26 @ 3:57 AM
NCT ID:
NCT01613118
Group ID:
EG004
Title:
All Sparsentan (Double-Blind and Open-Label Extension)
Description:
Double-blind and open-label extension data for all patients while on sparsentan (RE-021). This includes double-blind and open-label extension data for subjects randomized to sparsentan, and only open-label extension data for subjects randomized to irbesartan.
Sparsentan (RE-021): Oral, once-daily
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
48
Serious Number At Risk:
108
Other Number Affected:
104
Other Number At Risk:
108
Study:
NCT01613118
Results Section:
NCT01613118
Adverse Events Module:
NCT01613118