Overview

Assess the Long Term Efficacy and Safety of Ruxolitinib Cream in Participants With Vitiligo

Status:
Recruiting
Trial end date:
2024-01-18
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to evaluate the duration of response following withdrawal of ruxolitinib cream (Cohort A vehicle group), safety and maintenance of response with continued use of ruxolitinib cream in participants who have completed either Study NCT04052425 or NCT04057573 (parent studies) in which the participants will have been using ruxolitinib cream BID for the previous 28 to 52 weeks depending on their initial randomization in the parent study.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Incyte Corporation
Criteria
Inclusion Criteria:

- Currently enrolled and receiving treatment in INCB 18424-306 (NCT04052425) or INCB
18424-307 (NCT04057573) studies evaluating ruxolitinib cream in participants with
vitiligo.

- Currently tolerating ruxolitinib cream in the parent study and no safety concerns per
investigators judgment.

- Has demonstrated compliance, as assessed by the investigator, with the parent study
protocol requirements.

- Willingness and ability to comply with scheduled visits, treatment plans, and any
other study procedures indicated in this protocol.

- Male and female participants must be willing to take appropriate contraceptive
measures to avoid pregnancy or fathering a child.

- Ability to comprehend and willingness to sign an ICF or written informed consent of
the parent(s) or legal guardian and written assent from the participant when possible.

Exclusion Criteria:

- Has been permanently discontinued from study treatment in the parent study for any
reason.

- Participants with an uncontrolled intercurrent illness or any concurrent condition
that, in the investigator's opinion, would jeopardize the safety of the participant or
compliance with the Protocol.

- Pregnant or breastfeeding woman.

- Participants who live with anyone participating in any current Incyte-sponsored
ruxolitinib cream study.