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 @ 4:55 PM
Ignite Modification Date:
2025-12-25 @ 2:37 PM
NCT ID:
NCT02926950
Group ID:
EG001
Title:
Sotagliflozin 400 mg + Metformin
Description:
Following a 2-week run-in period, Sotagliflozin 400 mg was administered as 2 tablets, once daily, before the first meal of the day plus Metformin as prescribed by the Principal Investigator for up to 26 weeks in the double-blind Core Treatment Period, and participants continued the same treatment in the double-blind Extension Period for up to 53 weeks.
Deaths Number Affected:
3
Deaths Number At Risk:
None
Serious Number Affected:
19
Serious Number At Risk:
259
Other Number Affected:
85
Other Number At Risk:
259
Study:
NCT02926950
Results Section:
NCT02926950
Adverse Events Module:
NCT02926950