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 @ 12:56 AM
Ignite Modification Date:
2025-12-25 @ 11:11 PM
NCT ID:
NCT03781167
Group ID:
EG001
Title:
ABBV-951 High Dose Subgroup
Description:
After a 4-week Optimization Period, participants continued receiving ABBV-951 by continuous subcutaneous infusion (CSCI) during the 48-week Maintenance Period. Participants whose modal total daily dose (most frequent dose) over the entire study was ≥ 2530 mg of Foslevodopa/day were analyzed as the High Dose Subgroup.
Deaths Number Affected:
5
Deaths Number At Risk:
None
Serious Number Affected:
31
Serious Number At Risk:
113
Other Number Affected:
107
Other Number At Risk:
113
Study:
NCT03781167
Results Section:
NCT03781167
Adverse Events Module:
NCT03781167