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Enfortumab Vedotin, Pembrolizumab and Quemliclustat for the Treatment of Unresectable Locally Advanced and Metastatic Urothelial Cancer

16 de septiembre de 2026 actualizado por: Fred Hutchinson Cancer Center

A Phase Ib/II Study to Evaluate the Safety and Efficacy of Enfortumab Vedotin Plus Pembrolizumab in Combination With Quemliclustat in Unresectable Locally Advanced and Metastatic Urothelial Carcinoma

This phase Ib/II trial tests the safety, side effects, and best dose of quemliclustat in combination with enfortumab vedotin and pembrolizumab, and to see how well the combination works for the treatment of bladder, renal pelvis, or ureter urothelial cancer that cannot be removed by surgery (unresectable), that has spread to nearby tissue or lymph nodes (locally advanced) or that has spread from where it first started (primary site) to other places in the body (metastatic). Enfortumab vedotin is a monoclonal antibody, enfortumab, linked to an anticancer drug called vedotin. It works by helping the immune system to slow or stop the growth of cancer cells. Enfortumab attaches to a protein called nectin-4 on cancer cells in a targeted way and delivers vedotin to kill them. It is a type of antibody-drug conjugate. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Quemliclustat may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving quemliclustat in combination with enfortumab vedotin and pembrolizumab and may be safe, tolerable and/or effective in treating patients with unresectable locally advanced and metastatic urothelial cancer.

Descripción general del estudio

Descripción detallada

OUTLINE:

Patients receive quemliclustat intravenously (IV) on day 1, enfortumab vedotin IV on days 1 and 8 and pembrolizumab IV on day 1 of each cycle. Cycles repeat every 21 days for 2 years in the absence of disease progression or unacceptable toxicity. Patients may undergo tumor biopsy during screening and optionally undergo throughout the study. Patients also undergo computed tomography (CT)/magnetic resonance imaging (MRI) and blood sample collection throughout the study.

After completion of study treatment, patients are followed up within 30 days and then every 12 weeks for 3 years.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

27

Fase

  • Fase 2
  • Fase 1

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

  • Nombre: Rosa Nadal Rios, MD, PhD
  • Número de teléfono: 206-598-3300
  • Correo electrónico: rnadalri@fredhutch.org

Ubicaciones de estudio

    • Washington
      • Seattle, Washington, Estados Unidos, 98109
        • Reclutamiento
        • Fred Hutch/University of Washington Cancer Consortium
        • Investigador principal:
          • Rosa Nadal Rios, MD, PhD
        • Contacto:

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

Inclusion Criteria:

  • Participants must be at least 18 years of age on the day of signing informed consent. Participant (or legally authorized representative if applicable) provides written informed consent for trial
  • Participants must have previously untreated locally advanced or metastatic bladder cancer including bladder cancer [stage IIIB: T1-T4N2-3M0, stage IVa: T4bAnyNM0 or AnyTAnyNM1a, and stage IVB: AnyTAnyNM1b clinical stage per American Joint Commission on Cancer (AJCC)] or renal pelvis or ureter cancer [stage IV: T4Nx-0M0, AnyTN1-2M0, AnyTAnyNM1 clinical stage per AJCC]. Lymph node with ≥ 15 mm short axis or biopsy-positive for carcinoma will be considered pathologically enlarged and measurable
  • Participants must have either conventional urothelial carcinoma or urothelial carcinoma variants. A review of pathology by a local expert genitourinary (GU) pathologist is required to confirm the diagnosis. Any component (%) of non-conventional urothelial noted on tumor specimen is allowed for only histologic subtypes listed below in up to 20% of participants enrolled in this study.

    • Urothelial carcinoma with squamous differentiation
    • Urothelial carcinoma with glandular differentiation
    • Urothelial carcinoma with trophoblastic differentiation
    • Nested urothelial carcinoma
    • Tubular and microcystic urothelial carcinoma
    • Micropapillary urothelial carcinoma
    • Lymphoepithelioma-like urothelial carcinoma
    • Plasmacytoid urothelial carcinoma
    • Sarcomatoid urothelial carcinoma
    • Giant cell urothelial carcinoma
    • Lipid-rich urothelial carcinoma
    • Clear cell (glycogen rich) urothelial carcinoma
    • Poorly differentiated urothelial carcinoma
    • Squamous cell neoplasms including pure squamous cell carcinomas, verrucous carcinomas and squamous cell papilloma
  • Measurable disease by RECIST v 1.1
  • Participants must have an Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0-2
  • Available baseline fresh biopsy tissue sample obtained in the protocol RG1712006 though clinically indicated procedures or participants must be willing to undergo a baseline research biopsy when safe and feasible
  • Participant must have an estimated life expectancy of at least 3 months
  • Hemoglobin ≥ 9 gr/dl
  • Absolute neutrophil count: ≥ 1500/ µL
  • White blood cell count: ≥ 3000/µL
  • Absolute lymphocyte count: ≥ 1000/µL
  • Platelet count: ≥ 100.000/µL (without transfusion support)
  • Serum aspartate aminotransferase (AST) and alanine aminotransferase (ALT): ≤ 2.5 x upper limit of normal (ULN)
  • Total bilirubin: ≤ 1.5 mg/dl except for patients with Gilbert's syndrome who must have a total bilirubin ≤ 3 mg/dl
  • Creatinine clearance: ≥ 30 ml/min/1.73m^2 by the method of Chronic Kidney Disease Epidemiology Collaboration (CKI-EPI) or ≥ 30 ml/min by the method of 24 hour (h) clearance of creatinine calculation
  • International Normalized Ratio (INR): < 1.5

Exclusion Criteria:

  • Participants who are receiving any other investigational agents or concurrent anticancer treatment. Participants must have adequate treatment washout period before treatment, defined as: Major surgery (≥ 4 weeks), palliative radiation therapy (≥ 1 weeks from completion of treatment if they have recovered from the acute toxic effect of radiotherapy), prior adjuvant immunotherapy (≥ 4 weeks)
  • Participants whose tumors have any % neuroendocrine or small cell histology, glandular neoplasms, urachal carcinomas, tumor of mullerian type, mesenchymal tumors or urothelial tract hematopoietic and lymphoid tumors
  • Participants considered to be medically unfit for EV-P regimen as per Investigator discretion
  • Participants with concurrent use of systemic steroids (within 10 days of enrollment), except for physiologic doses of systemic steroid replacement or local (topical, nasal, intraarticular or inhaled) steroid use
  • Participants who have experienced disease progression following neoadjuvant or adjuvant systemic therapy within 12 months prior to enrollment will not be eligible
  • Patients with Fridericia's corrected QT interval (QTcF) interval at screening of > 480 milliseconds.

    • Note: For any QTcF > 480 milliseconds on initial electrocardiogram (ECG), a follow-up ECG will be performed to confirm QTcF interval prolongation and exclude the patient from this study
  • Participants with active systemic autoimmune disease (e.g., lupus erythematosus, rheumatoid arthritis, Addison's disease, autoimmune disease associated with lymphoma, inflammatory bowel disease). Participants with autoimmune endocrine disorders controlled by medical management (e.g. thyroid disorders, type 1 diabetes, or adrenal insufficiency) will not be excluded
  • Participants who are known to be serologically positive for human immunodeficiency virus (HIV) and a CD4 count < 350 cells/microliter
  • Participants with known active hepatitis (i.e. Hepatitis B or C). Prior hepatitis (Hep) C infection is allowed as long as polymerase chain reaction (PCR) test is negative
  • Participants with clinically inactive brain metastases may be included. Participants with treated brain metastases that are no longer symptomatic and who require no treatment with corticosteroids or anticonvulsants may be included in the study if they have recovered from the acute toxic effect of radiotherapy. A minimum of 2 weeks must have elapsed between the end of whole-brain radiation therapy and study treatment
  • Participants with new or progressive brain metastases (less or equal of 1 cm of larger diameter) are eligible if the treating physician determines that immediate central nervous system (CNS) specific treatment is not required and is unlikely to be required for at least 4 weeks (or scheduled assessment after the first cycle of treatment), and a risk-benefit analysis (discussion) by the participant and the investigator favors participation in the clinical trial. Patients with leptomeningeal disease will be excluded
  • History or current evidence of any condition, therapy, or laboratory abnormality that might confound the results, interfere with the participant's participation for the full duration of the trial, or is not in the best interest of the participant to participate, in the opinion of the treating investigator
  • Participants with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy of assessment of the investigational regimen are eligible for this trial
  • Woman of childbearing potential with positive serum pregnancy test within 72 hours prior to enrollment. Active lactation is an exclusion criterion

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Treatment (enfortumab vedotin, pembrolizumab, quemliclustat)
Patients receive quemliclustat IV on day 1, enfortumab vedotin IV on days 1 and 8 and pembrolizumab IV on day 1 of each cycle. Cycles repeat every 21 days for 2 years in the absence of disease progression or unacceptable toxicity. Patients may undergo tumor biopsy during screening and optionally undergo throughout the study. Patients also undergo CT/MRI and blood sample collection throughout the study.
Someterse a una resonancia magnética
Otros nombres:
  • Resonancia magnética
  • Resonancia magnetica
  • Exploración de imágenes por resonancia magnética
  • Imágenes Médicas, Resonancia Magnética / Resonancia Magnética Nuclear
  • SRES
  • Imágenes de RM
  • Imágenes de RMN
  • RMN
  • Imágenes de resonancia magnética nuclear
  • Imágenes por resonancia magnética (IRM)
  • resonancia magnética nuclear
  • Imágenes por resonancia magnética (procedimiento)
  • Resonancias magnéticas
  • Resonancia magnética estructural
Dado IV
Otros nombres:
  • Keytruda
  • MK-3475
  • Lambrolizumab
  • SCH 900475
  • MK3475
  • SCH-900475
  • BCD-201
  • Pembrolizumab Biosimilar BCD-201
  • Pembrolizumab Biosimilar QL2107
  • QL2107
  • GME 751
  • GME751
  • Pembrolizumab Biosimilar GME751
  • MK 3475
  • SCH900475
  • Pembrolizumab Biosimilar RPH-075
  • RPH 075
  • RPH-075
  • RPH075
  • Pembrolizumab biosimilar SB27
  • SB 27
  • SB-27
  • SB27
Someterse a la recolección de muestras de sangre
Otros nombres:
  • Recolección de muestras biológicas
  • Muestra biológica recolectada
  • Coleccion de especimenes
  • Recolección de muestras
Someterse a una tomografía computarizada
Otros nombres:
  • Connecticut
  • GATO
  • Análisis de gato
  • Tomografía Axial Computarizada
  • Tomografía axial computarizada
  • Tomografía computarizada
  • tomografía
  • Tomografía axial computarizada (procedimiento)
  • Tomografía computarizada (TC)
  • Escaneo de gato de diagnóstico
  • Tipo de servicio de escaneo de gato de diagnóstico
Dado IV
Otros nombres:
  • ASG-22CE
  • Padcev
  • AGS22ME
  • AGS-22M6E
  • Anti-Nectina 4 ADC ASG-22CE
  • Conjugado de fármaco-anticuerpo monoclonal anti-nectina-4 AGS-22M6E
  • Enfortumab Vedotin-ejfv
  • ASG 22CE
  • ASG22CE
Someterse a biopsia tumoral
Otros nombres:
  • Caja
  • BIOPSIA_TIPO
Given IV
Otros nombres:
  • AB680
  • AB 680
  • AB-680
  • Inhibidor CD73 AB680

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Incidence of treatment related adverse events (Phase Ib)
Periodo de tiempo: From baseline, up to 21 days after last dose of investigational product
As measured by Common Terminology Criteria for Adverse Events version (v) 6.
From baseline, up to 21 days after last dose of investigational product
Overall response rate (ORR) (Phase II)
Periodo de tiempo: From baseline, up to disease progression or unacceptable side effects, up to 3 years after completion of study treatment
Assessed by Response Evaluation Criteria in Solid Tumors (RECIST) v 1.1. Will calculate the count and percentage with a 95% confidence interval (CI).
From baseline, up to disease progression or unacceptable side effects, up to 3 years after completion of study treatment

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
ORR (Phase Ib)
Periodo de tiempo: From baseline, up to disease progression or unacceptable side effects, up to 3 years after completion of study treatment
Assessed by RECIST v 1.1. Will calculate the count and percentage with a 95% CI.
From baseline, up to disease progression or unacceptable side effects, up to 3 years after completion of study treatment
Complete response rate (Phase II)
Periodo de tiempo: From baseline, up to disease progression or unacceptable side effects, up to 3 years after completion of study treatment
Assessed by RECIST v 1.1. Will calculate the count and percentage with a 95% CI.
From baseline, up to disease progression or unacceptable side effects, up to 3 years after completion of study treatment
Duration of response (Phase II)
Periodo de tiempo: From response (ORR) until disease progression or unacceptable side effects or death which occurs earlier, up to 3 years after completion of study treatment
Will use Kaplan Meier method to estimate the survival curve, median and its corresponding 95% CI.
From response (ORR) until disease progression or unacceptable side effects or death which occurs earlier, up to 3 years after completion of study treatment
Progression free survival (Phase II)
Periodo de tiempo: From date of registration to date of first documentation of progression assessed by local review or symptomatic deterioration, or death due to any cause, up to 3 years after completion of study treatment
Will use Kaplan Meier method to estimate the survival curve, median and its corresponding 95% CI.
From date of registration to date of first documentation of progression assessed by local review or symptomatic deterioration, or death due to any cause, up to 3 years after completion of study treatment
Rate of consolidative therapy with cystectomy or chemoradiation with stage 3b (Phase II)
Periodo de tiempo: Up to 6 months
Will calculate the count and percentage with a 95% CI.
Up to 6 months

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Investigadores

  • Investigador principal: Rosa Nadal Rios, MD, PhD, Fred Hutch/University of Washington Cancer Consortium

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

15 de octubre de 2026

Finalización primaria (Estimado)

16 de julio de 2029

Finalización del estudio (Estimado)

16 de julio de 2029

Fechas de registro del estudio

Enviado por primera vez

18 de junio de 2026

Primero enviado que cumplió con los criterios de control de calidad

18 de junio de 2026

Publicado por primera vez (Actual)

25 de junio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

17 de septiembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

16 de septiembre de 2026

Última verificación

1 de junio de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

Sí

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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