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Topical Ruxolitinib in the Treatment of Adults With Pyoderma Gangrenosum (TRIUMPH)

20 sierpnia 2026 zaktualizowane przez: Alex Ortega Loayza, Oregon Health and Science University
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.

Przegląd badań

Status

Jeszcze nie rekrutacja

Szczegółowy opis

Pyoderma Gangrenosum is a rare, ulcerative inflammatory skin condition most commonly treated with systemic corticosteroids or cyclosporine, both of which carry significant long-term toxicity risks. Topical therapy has shown effectiveness for smaller lesions, but existing topical options (corticosteroids, calcineurin inhibitors) also carry risks with prolonged use and lack robust long-term safety data. Emerging evidence implicates the JAK-STAT signaling pathway in PG pathogenesis, with JAK1/2/3 and TYK2 found to be overexpressed in PG lesions and several PG-associated inflammatory cytokines (IFN-γ, IL-6, IL-12, IL-15, IL-23) acting through JAK-STAT-dependent mechanisms. Ruxolitinib, a selective JAK1/JAK2 inhibitor already FDA-approved as a topical cream for atopic dermatitis, has not previously been studied for PG in a clinical trial; prior evidence is limited to case reports of oral JAK inhibitors used off-label for PG.

This investigator-initiated trial will enroll approximately 12 adults (ages 18-99) with a PARACELSUS score >10 and a target ulcer ≤10 cm². Participants will apply ruxolitinib cream twice daily via a Topi-Click applicator for 24 weeks, continuing standard-of-care wound care throughout (cleansing, antimicrobial and hyper-absorbent dressings, compression, and debridement as needed). No additional systemic immunosuppressive therapy will be introduced during the study, though participants may remain on a stable pre-existing dose of a biologic for an associated autoimmune comorbidity.

The study includes 10 scheduled visits over 28 weeks (Screening, Weeks 0, 2, 4, 6, 8, 12, 16, 20, 24, 28), with select later visits available via telemedicine for participants living more than 30 miles from OHSU. Assessments include full body skin exams with ulcer measurement, high-frequency ultrasound imaging at Weeks 0, 6, 12, and 24, blood draws for safety labs (CBC, CMP, eGFR, ESR, CRP, G6PD, lipid panel) and infectious disease screening (HIV, HBV, HCV, TB), wound fluid collection for cytokine analysis, and patient-reported outcome measures (Skindex Mini, pain NRS, PHQ-9, GAD-7).

The primary endpoint is the proportion of participants achieving complete re-epithelialization of the target ulcer at Week 24. Secondary endpoints assessed by the investigator include Physician Global Assessment (PGA) scores, percent reduction in ulcer area, time to healing, time to recurrence, and treatment failure rate; secondary endpoints assessed by the participant include quality-of-life measured by Skindex Mini and pain reduction measured by NRS. Exploratory/mechanistic endpoints include changes in pro-inflammatory cytokine and chemokine expression in blood and lesional tissue, and ultrasound-based assessment of tissue remodeling during healing.

Participants who complete the study through Week 24 with a PGA score of 1-3 and no significant safety concerns will be eligible to enroll in a 48-week open-label extension, with continued dosing for as long as clinical benefit is observed, re-evaluated annually.

Typ studiów

Interwencyjne

Zapisy (Szacowany)

12

Faza

  • Faza 2

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Kontakt w sprawie studiów

  • Nazwa: Alexandra Shinde, MSc
  • Numer telefonu: 971-442-1620
  • E-mail: shindea@ohsu.edu

Kopia zapasowa kontaktu do badania

  • Nazwa: Chloe Vignola
  • Numer telefonu: 8-9045 503-418-9045
  • E-mail: vignola@ohsu.edu

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dorosły
  • Starszy dorosły

Akceptuje zdrowych ochotników

Nie

Opis

Inclusion Criteria:

  • Willingness to comply with study procedures/requirements
  • Capable of giving informed consent
  • Diagnosis of at least one PG ulcer by clinical, histological and laboratory assessments with a maximum wound size of 10 cm2.
  • Male age 18-99 who agree to not father a child or donate sperm while on study and at least 1 week following last dose of the study drug. If subject is a sexually active male and could cause a pregnancy, subject must be sure that female partner(s) are using birth control that works well or not have sex.
  • Female age 18-99; either of non-childbearing potential or of childbearing potential who test negative for pregnancy and agree to use at least two reliable methods of birth control or remain abstinent during the study and for at least 1 week following the last dose of ruxolitinib.
  • Classic type of PG defined with PARACELSUS score >10
  • Are candidates for topical therapy. Subjects on existing immunosuppression for managing underlying comorbidities associated with PG will be considered for trial and allowed to continue these medications while on trial
  • Patients on potent immunosuppressants (azathioprine, cyclosporine) or Janus kinase inhibitors will not be considered in the study
  • Patients may be on stable dose of prednisone 10 mg or less
  • Undergoing at least once a week standard of care wound care at home or wound care facility.
  • Willingness to travel to OHSU for all study visits, or living >30 miles from OHSU and willing/able to participate in remote videoconferencing visits with access to a computer with internet and webcam capabilities.

Exclusion Criteria:

  • Patients with pyoderma gangrenosum who have more than 3 ulcers measuring total >30 cm2
  • Have history of malignancy or lymphoproliferative disease; or have signs or symptoms suggestive of possible lymphoproliferative disease, including lymphadenopathy or splenomegaly; or have active primary or recurrent malignant disease; or have been in remission from clinically significant malignancy for < 5years.
  • Patients with cervical carcinoma in situ, basal cell carcinoma or squamous cell carcinomas who have had active disease within 3 years of screening for this study.
  • Active, untreated, acute or chronic infection (such as untreated tuberculosis), or immunocompromised to an extent that such that participation in the study would pose an unacceptable risk to the subject. (Treated infections such as latent tuberculosis after completion of the appropriate therapy are not excluded.)
  • Clinically serious infection or received intravenous antibiotics for an infection, within 4 weeks of randomization.
  • Active viral infection that, based on the investigator's clinical assessment, makes the subject and unsuitable candidate for the study.
  • Positive for human immunodeficiency virus, hepatitis B virus, or hepatitis C virus.
  • Symptomatic herpes zoster infection within 12 weeks of screening or recurrent or disseminated (even a single episode) herpes zoster.
  • Symptomatic herpes simplex at the time of randomization or disseminated (even a single episode) herpes simplex
  • History of disseminated opportunistic infections (e.g., listeriosis and histoplasmosis).
  • Have a history of VTE, or are considered at high risk for VTE as deemed by the investigator, or have 2 or more of the following risk factors for VTE:

    1. Aged >65 years.
    2. BMI >35 kg/m2.
    3. Oral contraceptive use and current smoker.
  • Wound care debridement of any PG ulcer within 2 weeks
  • Patients receiving regular intralesional corticosteroid treatment to manage PG or underlying comorbidities associated with PG will be allowed to continue intralesional corticosteroid treatment during screening and while on study
  • Previous exposure to a systemic JAK inhibitor (ruxolitinib, tofacitinib, upadacitinib, filgotinib) or topical JAK inhibior.
  • Clinically significant (per investigator's judgement) drug or alcohol abuse within the last 6 months preceding the Baseline Visit.
  • Had any major surgery within 8 weeks prior to baseline or will require major surgery during the study, which in the opinion of the investigator would pose an unacceptable risk to the subject.
  • Recent (within past 6 months) cerebrovascular accident, myocardial infarction, coronary stenting. Uncontrolled hypertension - confirmed systolic blood pressure >160 mmHg or diastolic blood pressure >100 mm Hg.
  • Presence of significant uncontrolled respiratory, hepatic, renal, endocrine, hematologic, neurologic, or neuropsychiatric disorders, or abnormal laboratory screening values that, in the opinion of the investigator, pose an unacceptable risk to the subject if participating in the study or of interfering with the interpretation of the data.
  • Have clinical laboratory test results at screening that are outside the normal reference range of the population and are considered clinically significant, or have any of the following specific abnormalities:
  • Neutrophil count <1500 cells/µL
  • lymphocyte count <500 cells/µL
  • platelet count <100,000 cells/µL,
  • AST or ALT > 2.5 Women who are lactating or breastfeeding.
  • Have any other condition that precludes the subject from following and completing the protocol, in the opinion of the investigator.
  • Are investigator site personnel directly affiliated with this study and/or their immediate families (spouse, parent, child, or sibling).
  • Are currently enrolled in, or discontinued from a clinical trial involving an investigational product or non-approved use of a drug or device within the last 4 weeks or a period of at least 5 half-lives of the last administration of the drug, whichever is longer, or concurrently enrolled in any other type of medical research judged not to be scientifically or medically compatible with this study
  • Have and/or are managing a substance use disorder involving opioids and/or cannabinoids

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Nie dotyczy
  • Model interwencyjny: Zadanie dla jednej grupy
  • Maskowanie: Brak (otwarta etykieta)

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: Treatment
Treated with topical ruxolitinib thin laywer twice daily for 24 weeks.
topical ruxolitinib 1.5% cream applied to wound bed twice daily for 24 weeks.
Inne nazwy:
  • OPZELURA

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Complete healing of target ulcer
Ramy czasowe: Up to 24 weeks
The proportion of patients with complete re-epithelization, defined as 100% re-epithelialization without any drainage, of the target ulcer at week 24.
Up to 24 weeks

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
PGA between 0-1
Ramy czasowe: Through week 24

1. Assessing the proportion of patients that show target ulcer healing in response to study treatment as measured by achieving PGA between 0 and 1 after treatment with baricitinib at week-24. This scale has been used in previous trials: 0 = total resolution of target ulcer with no signs of active PG

1= almost completely healed target ulcer with only minimal signs of active PG 2 = evidence of target ulcer healing which involves at least 50% of ulcer/ulcer margin 3 = evidence of target ulcer healing which involves less than 50% of ulcer/margin 4 = no evidence of target healing ulcer

Through week 24
Number of participants with treatment-related adverse events as assessed by CTCAE v4.0
Ramy czasowe: Through week 24
To determine the safety of ruxolitinib for the treatment of subjects with PG who are candidates for systemic therapy, by the number of participants who experienced treatment-related adverse events while on study.
Through week 24
Impact of skin disease on quality of life using Skindex Mini
Ramy czasowe: By week 28
A 3-item questionnaire assessing three domains of quality of life impact; symptoms, emotions, and function related to skin disease on a scale of 0 (never bothered) to 5 (always bothered)
By week 28
Quality of life via Participant Global Assessment
Ramy czasowe: By week 28
Measures an individual's overall impression of their health, disease severity, or treatment response on a scale of clear to severe.
By week 28
Quality of life via Participant Physical Function Assessment
Ramy czasowe: By week 28
Evaluates an individual's ability to perform daily activities, mobility, strength, balance, and overall functional capacity on a scale from "no difficulty at all" to "can't do because of ulcer"
By week 28
Patient Health Questionnaire-9
Ramy czasowe: By week 28
Measures the presence and severity of depressive symptoms over the past two weeks in 9 questions ranking on a scale of "Not at all" to "Nearly every day".
By week 28
Generalized Anxiety Disorder Assessment
Ramy czasowe: By week 28
Measures the severity of generalized anxiety disorder symptoms over the past two weeks in 7 questions ranking on a scale of "not at all" to "nearly every day".
By week 28
Pain improvement determined by Numeric Rating Scale (NRS)
Ramy czasowe: Through week 24
To determine the improvement in pain by NRS scale in the last 7 days and the peak pain by NRS scale in the last 24 hours from 0 (no pain/sensation) to 10 (worst possible pain/sensation)
Through week 24
Time to healing
Ramy czasowe: Through week 24
Determine time to healing
Through week 24
Time to recurrence
Ramy czasowe: Through week 24
Determine time to recurrence, appearance of new ulcer after complete closure
Through week 24

Inne miary wyników

Miara wyniku
Opis środka
Ramy czasowe
Cytokine markers changed due to treatment
Ramy czasowe: Through week 24
Evaluation of cytokine gene expression before and after treatment in skin and blood samples
Through week 24
Evaluate imaging structures using HFUS
Ramy czasowe: Through week 24
Use high-frequency ultrasound imaging to predict healing via the presence of hyperechoic oval structures, hair tracts, and U-shaped vessels.
Through week 24

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Publikacje i pomocne linki

Osoba odpowiedzialna za wprowadzenie informacji o badaniu dobrowolnie udostępnia te publikacje. Mogą one dotyczyć wszystkiego, co jest związane z badaniem.

Publikacje ogólne

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Szacowany)

1 września 2026

Zakończenie podstawowe (Szacowany)

1 września 2029

Ukończenie studiów (Szacowany)

1 grudnia 2029

Daty rejestracji na studia

Pierwszy przesłany

29 lipca 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

20 sierpnia 2026

Pierwszy wysłany (Rzeczywisty)

24 sierpnia 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

24 sierpnia 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

20 sierpnia 2026

Ostatnia weryfikacja

1 sierpnia 2026

Więcej informacji

Terminy związane z tym badaniem

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

NIEZDECYDOWANY

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Tak

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

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