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 @ 10:00 PM
Ignite Modification Date:
2025-12-25 @ 7:37 PM
NCT ID:
NCT05593432
Group ID:
EG001
Title:
Ruxolitinib Cream 1.5% BID
Description:
Participants who applied ruxolitinib cream 1.5% BID for 16 weeks during the Double-Blind, Vehicle-Controlled Period plus participants who completed the Week 16 assessments with no safety concerns, continued into the Open-label Extension Period, and applied ruxolitinib cream 1.5% BID for an additional 16 weeks
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
60
Other Number Affected:
14
Other Number At Risk:
60
Study:
NCT05593432
Results Section:
NCT05593432
Adverse Events Module:
NCT05593432