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 @ 2:00 AM
Ignite Modification Date:
2025-12-26 @ 12:23 AM
NCT ID:
NCT03285594
Group ID:
EG002
Title:
Sotagliflozin 400 mg
Description:
Following a 4-week run-in period, participants were randomized to sotagliflozin 400 mg administered as 2 tablets, once daily, before the first meal of the day in the double-blind treatment period for up to 54.6 weeks. Background therapy with insulin glargine (with or without OADs) continued throughout the study.
Deaths Number Affected:
6
Deaths Number At Risk:
None
Serious Number Affected:
28
Serious Number At Risk:
285
Other Number Affected:
45
Other Number At Risk:
285
Study:
NCT03285594
Results Section:
NCT03285594
Adverse Events Module:
NCT03285594