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:
EG001
Title:
RE-021 (Sparsentan) 400 mg - Double-Blind Period
Description:
Sparsentan (RE-021) administered as a single oral morning dose. In this ARM the sparsentan (RE-021) dose was 400mg.
Patients at \</= 50kg received half the sparsentan (RE-021) dose for the 8 week duration.
Sparsentan (RE-021): Oral, once-daily
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
26
Other Number Affected:
17
Other Number At Risk:
26
Study:
NCT01613118
Results Section:
NCT01613118
Adverse Events Module:
NCT01613118