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 @ 5:21 PM
Ignite Modification Date:
2025-12-25 @ 2:56 PM
NCT ID:
NCT03011450
Group ID:
EG002
Title:
K-877: 40-Week Extension
Description:
* Participants randomized to receive K-877 0.2 mg tablets twice daily in the 12-week Efficacy Period continued to receive K-877 0.2 mg tablets BID in the 40-week Extension Period
* Only AEs with onset in the 40-week extension period are included.
Deaths Number Affected:
3
Deaths Number At Risk:
None
Serious Number Affected:
25
Serious Number At Risk:
292
Other Number Affected:
2
Other Number At Risk:
292
Study:
NCT03011450
Results Section:
NCT03011450
Adverse Events Module:
NCT03011450