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 @ 11:48 PM
Ignite Modification Date:
2025-12-25 @ 9:42 PM
NCT ID:
NCT02787551
Group ID:
EG002
Title:
Fixed Ratio Combination Whole Study Period
Description:
Participants who completed core treatment period and met eligibility criteria entered in extension treatment period and received same treatment (FRC injected subcutaneously QD on top of OAD therapy) for 26 weeks (up to Week 52). Dose individually adjusted (median exposure: 365 days).
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
21
Serious Number At Risk:
206
Other Number Affected:
75
Other Number At Risk:
206
Study:
NCT02787551
Results Section:
NCT02787551
Adverse Events Module:
NCT02787551