Esta página foi traduzida automaticamente e a precisão da tradução não é garantida. Por favor, consulte o versão em inglês para um texto fonte.

A Study to Evaluate Dermal Open-Flow Microperfusion and Plasma Pharmacokinetic Study of Multiple Doses of Oral Povorcitinib or Topical Ruxolitinib Cream in Healthy Adult Participants

1 de junho de 2026 atualizado por: Incyte Corporation

An Open-Label, Dermal Open-Flow Microperfusion and Plasma Pharmacokinetic Study of Multiple Doses of Oral Povorcitinib or Topical Ruxolitinib Cream in Healthy Adult Participants

The purpose of this study is to evaluate the interstitial concentrations using the open-flow microperfusion device and plasma pharmacokinetics following multiple doses of povorcitinib or topical ruxolitinib cream in healthy adult participants.

Visão geral do estudo

Status

Recrutamento

Tipo de estudo

Intervencional

Inscrição (Estimado)

24

Estágio

  • Fase 1

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

  • Nome: Incyte Corporation Call Center (US)
  • Número de telefone: 1.855.463.3463
  • E-mail: medinfo@incyte.com

Estude backup de contato

  • Nome: Incyte Corporation Call Center (ex-US)
  • Número de telefone: +800 00027423
  • E-mail: eumedinfo@incyte.com

Locais de estudo

    • Minnesota
      • Dilworth, Minnesota, Estados Unidos, 56529
        • Recrutamento
        • Axis Clinicals

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Sim

Descrição

Inclusion Criteria:

  • Ability to comprehend and willingness to sign a written ICF for the study.
  • Aged 18 to 65 years, inclusive, at the time of signing the ICF.
  • Body mass index between 18.0 and 30.5 kg/m2, inclusive.
  • No clinically significant findings on screening evaluations (clinical, laboratory, and ECG).
  • Ability to swallow and retain oral medication.
  • Willingness to avoid pregnancy or fathering children.

Exclusion Criteria:

  • History of uncontrolled or unstable cardiovascular, respiratory, renal, gastrointestinal, endocrine, hematopoietic, psychiatric, and/or neurological disease within 6 months of screening.
  • Participants with any history of an autoimmune disease diagnosis.
  • History of cardiovascular, cerebrovascular, peripheral vascular, or thrombotic disease or uncontrolled hypertension.
  • History or presence of an abnormal ECG.
  • Presence or history of a malabsorption syndrome possibly affecting drug absorption (eg, Crohn's disease or chronic pancreatitis).
  • Any malignancies or history of malignancies with the exception of adequately treated or excised nonmetastatic basal cell or squamous cell cancer of the skin, or cervical carcinoma in situ.
  • Current or recent (within 3 months of screening) clinically significant gastrointestinal disease or surgery (including cholecystectomy; excluding appendectomy and hernia repair) that could affect the absorption of study drug.
  • Any major surgery within 4 weeks of screening.
  • Donation of blood to a blood bank or participation in a clinical study (except a screening visit) within 4 weeks of screening (within 2 weeks for plasma-only donation).
  • Blood transfusion within 4 months of check-in (Day -1).
  • Chronic or current active infectious disease requiring systemic antibiotic, antifungal, or antiviral treatment (includes latent treated tuberculosis).
  • Known tuberculosis infection that is active or participant-reported history of tuberculosis or treatment thereof.
  • Positive test for HBV, HCV, or HIV. Participants whose results are compatible with prior immunization for or immunity due to infection with HBV may be included at the discretion of the investigator.
  • Has received a live vaccine (including attenuated) or anticipation of need for such a vaccine during the study within 3 months prior to the first dose of study drug. Note: Examples of live vaccines include but are not limited to the following: measles, mumps, rubella, chickenpox/zoster, yellow fever, rabies, Bacillus Calmette-Guérin, and typhoid. Seasonal influenza vaccines for injection are generally killed-virus vaccines and are allowed; however, intranasal influenza vaccines are live, attenuated vaccines and are not allowed.
  • Medical or self-reported history of alcoholism within 3 months of screening.
  • History of significant alcohol use within 3 months of screening, defined as regular alcohol consumption > 21 units per week for males and > 14 units for females (1 unit = 8 oz of beer or a 25 mL shot of 40% spirit, 1.5 to 2 units = 125 mL glass of wine, depending on type).
  • Positive urine or breath test for ethanol or positive urine or serum screen for drugs of abuse that are not otherwise explained by permitted concomitant medications or diet.
  • Current treatment or treatment within 30 days or 5 half-lives (whichever is longer) before the first dose of study treatment with another investigational medication or current enrollment in another investigational drug study.
  • Current treatment or treatment within 15 days or 5 half-lives (whichever is longer) before the first dose/application of study treatment with strong inducers or strong and moderate inhibitors of CYP3A4, P-gp, or BCRP (refer to the Drug Interaction Database for prohibited drugs.
  • Consumption of red wine, Seville oranges, grapefruit or grapefruit juice, pomelos, exotic citrus fruits, grapefruit hybrids, or fruit juices within 72 hours before the first dose of study drug.
  • History of any significant drug allergy (such as anaphylaxis or hepatotoxicity) deemed clinically relevant by the investigator.
  • Known hypersensitivity or severe reaction to povorcitinib or any excipients of povorcitinib, to ruxolitinib or any excipients of ruxolitinib or any JAK inhibitors.
  • Inability to undergo venipuncture or tolerate venous access.
  • History of tobacco or nicotine containing product use within 1 month of screening.
  • Use of prescription drugs (including hormonal contraceptives) within 14 days of study treatment administration/application or nonprescription medications/products (including vitamins, minerals, and phytotherapeutic/herbal/plant-derived preparations) within 7 days before study treatment administration/application. However, occasional and standard dose paracetamol, acetaminophen, ibuprofen, and standard dose vitamins are permitted. Mega dose vitamins or supplements are not permissible.
  • Women who are pregnant or breastfeeding.
  • Any condition that would interfere with full participation in the study, including administration/application of study treatment and attending required study visits; pose a significant risk to the participant; or interfere with interpretation of study data.
  • Excessive exercise (ie Iron man®, triathlon, etc) within 7 days before check-in (Day -1).
  • Tattoo or scarring at skin sample sites.
  • Participants prone to keloid or hypertrophic scar formation or any known wound healing disorder.
  • Not willing to avoid excessive sun exposure, steam baths, sauna, swimming, and other strenuous activities for 14 days after Day 12 to ensure good tissue regeneration.
  • Pronounced hairiness on the planned application sites, dOFM probe insertion sites, and skin biopsy collection sites, that may negatively affect dose application, probe placement, and/or sample testing.
  • Not willing to refrain from shaving the planned application sites, dOFM probe insertion sites, and skin biopsy collection sites, or using skin care products on the planned application sites, dOFM probe insertion sites, and skin biopsy collection sites, for at least 5 days before Day 1.
  • Not willing to avoid sunbathing, using tanning salons, or using spray/lotion tanning agents within 7 days prior to Day 1 dose administration/application.
  • Presence of needle phobia.
  • Increased risk of thrombosis (eg, personal or first-degree relative[s] history of deep vein thrombosis).

Other protocol-defined Inclusion/Exclusion Criteria may apply.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Não randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Cohort 1: Ruxolitinib 1.5 % Cream
Ruxolitinib cream applied topically twice daily.
Ruxolitinib cream applied topically.
Experimental: Cohort 2: Povorcitinib
Povorcitinib will be administered at the protocol defined dose.
Oral; Tábua
Outros nomes:
  • INCB054707
Experimental: Cohort 3: Povorcitinib
Povorcitinib will be administered at the protocol defined dose.
Oral; Tábua
Outros nomes:
  • INCB054707

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Pharmacokinetics Parameter (PK): Cmax of dermal interstitial fluid (dISF) ruxolitinib
Prazo: Up to Day 12
Defined as the maximum observed plasma concentration.
Up to Day 12
Pharmacokinetics Parameter: AUClast of dISF ruxolitinib
Prazo: Up to Day 12
Defined as the area under the concentration-time curve from time zero to the last quantifiable concentration.
Up to Day 12
Pharmacokinetics Parameter: AUC∞ of dISF ruxolitinib
Prazo: Up to Day 12
Defined as the area under the plasma concentration-time curve extrapolated to time of infinity.
Up to Day 12
Pharmacokinetics Parameter: Cmax of dISF povorcitinib
Prazo: Up to Day 12
Defined as the maximum observed plasma concentration.
Up to Day 12
Pharmacokinetics Parameter: AUClast of dISF povorcitinib
Prazo: Up to Day 12
Defined as the area under the concentration-time curve from time zero to the last quantifiable concentration.
Up to Day 12
Pharmacokinetics Parameter: AUC∞ of dISF povorcitinib
Prazo: Up to Day 12
Defined as the area under the plasma concentration-time curve extrapolated to time of infinity.
Up to Day 12
Pharmacokinetics Parameter: Cmax of plasma ruxolitinib
Prazo: Up to Day 12
Defined as the maximum observed plasma concentration.
Up to Day 12
Pharmacokinetics Parameter: AUClast of plasma ruxolitinib
Prazo: Up to Day 12
Defined as the area under the concentration-time curve from time zero to the last quantifiable concentration.
Up to Day 12
Pharmacokinetics Parameter: AUC∞ of plasma ruxolitinib
Prazo: Up to Day 12
Defined as the area under the plasma concentration-time curve extrapolated to time of infinity.
Up to Day 12
Pharmacokinetics Parameter: Cmax of plasma povorcitinib
Prazo: Up to Day 12
Defined as the maximum observed plasma concentration.
Up to Day 12
Pharmacokinetics Parameter: AUClast of plasma povorcitinib
Prazo: Up to Day 12
Defined as the area under the concentration-time curve from time zero to the last quantifiable concentration.
Up to Day 12
Pharmacokinetics Parameter: AUC∞ of plasma povorcitinib
Prazo: Up to Day 12
Defined as the area under the plasma concentration-time curve extrapolated to time of infinity.
Up to Day 12

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Number of participants with Treatment-emergent Adverse Events (TEAEs)
Prazo: Up to Day 28
Defined as any adverse event, either reported for the first time or the worsening of a pre-existing event, occurring after first dose of study treatment.
Up to Day 28
Pharmacokinetics Parameter: tmax of dISF ruxolitinib
Prazo: Up to Day 12
Defined as the time to maximum concentration.
Up to Day 12
Pharmacokinetics Parameter: t½ of dISF ruxolitinib
Prazo: Up to Day 12
Defined as the apparent terminal-phase disposition half-life.
Up to Day 12
Pharmacokinetics Parameter: CL/F of dISF ruxolitinib
Prazo: Up to Day 12
Defined as the apparent clearance.
Up to Day 12
Pharmacokinetics Parameter: Vz/F of dISF ruxolitinib
Prazo: Up to Day 12
Defined as the apparent volume of distribution.
Up to Day 12
Pharmacokinetics Parameter: λz of dISF ruxolitinib
Prazo: Up to Day 12
Defined as the terminal-phase disposition rate constant.
Up to Day 12
Pharmacokinetics Parameter: tmax of dISF povorcitinib
Prazo: Up to Day 12
Defined as the time to maximum concentration.
Up to Day 12
Pharmacokinetics Parameter: t½ of dISF povorcitinib
Prazo: Up to Day 12
Defined as the apparent terminal-phase disposition half-life.
Up to Day 12
Pharmacokinetics Parameter: CL/F of dISF povorcitinib
Prazo: Up to Day 12
Defined as the apparent clearance.
Up to Day 12
Pharmacokinetics Parameter: Vz/F of dISF povorcitinib
Prazo: Up to Day 12
Defined as the apparent volume of distribution.
Up to Day 12
Pharmacokinetics Parameter: λz of dISF povorcitinib
Prazo: Up to Day 12
Defined as the terminal-phase disposition rate constant.
Up to Day 12
Pharmacokinetics Parameter: tmax of plasma ruxolitinib
Prazo: Up to Day 12
Defined as the time to maximum concentration.
Up to Day 12
Pharmacokinetics Parameter: t½ of plasma ruxolitinib
Prazo: Up to Day 12
Defined as the apparent terminal-phase disposition half-life.
Up to Day 12
Pharmacokinetics Parameter: CL/F of plasma ruxolitinib
Prazo: Up to Day 12
Defined as the apparent clearance.
Up to Day 12
Pharmacokinetics Parameter: Vz/F of plasma ruxolitinib
Prazo: Up to Day 12
Defined as the apparent volume of distribution.
Up to Day 12
Pharmacokinetics Parameter: λz of plasma ruxolitinib
Prazo: Up to Day 12
Defined as the terminal-phase disposition rate constant.
Up to Day 12
Pharmacokinetics Parameter: tmax of plasma povorcitinib
Prazo: Up to Day 12
Defined as the time to maximum concentration.
Up to Day 12
Pharmacokinetics Parameter: t½ of plasma povorcitinib
Prazo: Up to Day 12
Defined as the apparent terminal-phase disposition half-life.
Up to Day 12
Pharmacokinetics Parameter: CL/F of plasma povorcitinib
Prazo: Up to Day 12
Defined as the apparent clearance.
Up to Day 12
Pharmacokinetics Parameter: Vz/F of plasma povorcitinib
Prazo: Up to Day 12
Defined as the apparent volume of distribution.
Up to Day 12
Pharmacokinetics Parameter: λz of plasma povorcitinib
Prazo: Up to Day 12
Defined as the terminal-phase disposition rate constant.
Up to Day 12

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Patrocinador

Investigadores

  • Diretor de estudo: Incyte Medical Monitor, Incyte Corporation

Publicações e links úteis

A pessoa responsável por inserir informações sobre o estudo fornece voluntariamente essas publicações. Estes podem ser sobre qualquer coisa relacionada ao estudo.

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

18 de maio de 2026

Conclusão Primária (Estimado)

3 de setembro de 2026

Conclusão do estudo (Estimado)

19 de setembro de 2026

Datas de inscrição no estudo

Enviado pela primeira vez

8 de maio de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

8 de maio de 2026

Primeira postagem (Real)

14 de maio de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

3 de junho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

1 de junho de 2026

Última verificação

1 de junho de 2026

Mais Informações

Termos relacionados a este estudo

Palavras-chave

Termos MeSH relevantes adicionais

Outros números de identificação do estudo

  • INCB054707-113

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Sim

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

Se inscrever