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 @ 11:41 PM
Ignite Modification Date:
2025-12-25 @ 9:32 PM
NCT ID:
NCT01140451
Group ID:
EG001
Title:
Placebo/Ataluren
Description:
Participants who received double-blind placebo during Study 009 received open-label ataluren TID: 10 mg/kg of body weight with breakfast, 10 mg/kg with lunch, and 20 mg/kg with dinner (total dose 40 mg/kg/day), for up to 96 weeks. Participants were followed for 4 weeks after treatment.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
57
Serious Number At Risk:
96
Other Number Affected:
94
Other Number At Risk:
96
Study:
NCT01140451
Results Section:
NCT01140451
Adverse Events Module:
NCT01140451