12 Participants NeededMy employer runs this trial

Topical Ruxolitinib for Pyoderma Gangrenosum

(TRIUMPH Trial)

AS
Overseen ByAlexandra Shinde, MSc
Age: 18+
Sex: Any
Trial Phase: Phase 2
Sponsor: Oregon Health and Science University
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This is a single-center, open-label, single-arm pilot study evaluating topical ruxolitinib (OPZELURA) as a treatment for adults with Pyoderma Gangrenosum (PG), a chronic inflammatory skin condition that causes painful ulcers. Approximately 12 participants will apply ruxolitinib cream twice daily for 24 weeks while continuing standard wound care, with the goal of determining whether the drug helps target ulcers heal completely without the need for systemic immunosuppressive therapy. Participants will be followed for a total of 28 weeks, with the option to continue treatment in a 48-week open-label extension if they respond well and remain safe on the drug. The study is sponsored by Oregon Health \& Science University and funded by Incyte Corporation.

Are You a Good Fit for This Trial?

This trial is for adults (18-99) with a confirmed diagnosis of pyoderma gangrenosum and at least one ulcer no larger than 10 cm². Participants must be able to follow study procedures, use reliable birth control if needed, and can continue certain stable medications but not strong immunosuppressants or other JAK inhibitors.

Inclusion Criteria

I am willing to follow all study procedures and requirements.
I am taking 10 mg or less of prednisone daily and my dose is stable.
I have at least one diagnosed PG ulcer no larger than 10 cm2.
See 7 more

What Are the Treatments Tested in This Trial?

Interventions

  • topical ruxolitinib

Trial Overview

The study tests ruxolitinib cream (1.5%) applied twice daily for up to 24 weeks on skin ulcers caused by pyoderma gangrenosum, alongside standard wound care. All participants receive the same treatment in this single-arm pilot study.

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: TreatmentExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Oregon Health and Science University

Lead Sponsor

Trials
1,024
Recruited
7,420,000+

Incyte Corporation

Industry Sponsor

Trials
408
Recruited
66,800+
Steven Stein profile image

Steven Stein

Incyte Corporation

Chief Medical Officer since 2015

MD from University of Witwatersrand

Hervé Hoppenot profile image

Hervé Hoppenot

Incyte Corporation

Chief Executive Officer since 2014

MBA from ESSEC Business School