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 @ 8:02 PM
Ignite Modification Date:
2025-12-25 @ 5:35 PM
NCT ID:
NCT03099304
Group ID:
EG004
Title:
Ruxolitinib Cream 1.5% BID
Description:
All participants who received at least one dose of ruxolitinib cream 1.5% BID. Treatment was received by (1) participants randomized to ruxolitinib cream 1.5% BID through Week 156, (2) participants who were randomized to the vehicle group or were randomized to ruxolitinib cream 0.15% QD and did not achieve 25% improvement in F-VASI score at Week 24 and crossed over to 1.5% BID for 28 weeks (Week 24 to Week 52 \[continued double-blind treatment period\]), and (3) participants who were (a) randomized to the vehicle group, (b) to ruxolitinib cream 0.15% QD and achieved 25% improvement in F-VASI score at Week 24, (c) to ruxolitinib cream 0.5% QD, and (d) to ruxolitinib cream 1.5% QD who crossed over to 1.5% BID during the open-label extension period.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
4
Serious Number At Risk:
130
Other Number Affected:
45
Other Number At Risk:
130
Study:
NCT03099304
Results Section:
NCT03099304
Adverse Events Module:
NCT03099304