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Phase II Trial of Zanzalitinib in Patients With Metastatic Castration Resistant Prostate Cancer

14 de septiembre de 2026 actualizado por: Pedro Barata, MD, MSc

A Single Arm Phase II Trial of Zanzalitinib in Patients With Metastatic Castration Resistant Prostate Cancer (mCRPC) With Soft Tissue or Visceral Metastases

This research study is for people with metastatic castrate-resistant prostate cancer (mCRPC). Zanzalintinib is a new drug that shows activity in mCRPC with soft tissue or visceral metastases who have progressed on prior treatment. Participants can stay in the research for up to 24 months as long as they experience clinical benefit from it. The purpose of this study is to learn if Zanzalinitib is effective in treating metastatic castrate-resistant prostate cancer.

Descripción general del estudio

Estado

Aún no reclutando

Intervención / Tratamiento

Descripción detallada

Prostate cancer is one of the most common cancers that affect males. Metastatic prostate cancer is treated at first with androgen deprivation therapy (ADT) and androgen receptor pathways inhibitors (ARPI). It is initially responsive to these treatments, but overtime it progresses from being hormone-sensitive to become castrate resistant, which leads to poorer outcomes. There have been other therapies that have been approved for treatment of metastatic castrate-resistant prostate cancer (mCRPC), but there are high-risk features such as high tumor burden, shorter time from diagnosis to metastatic disease, and presence of metastases that cause poor outcomes, with the overall survival being less than one year.

Zanzalintinib is a new drug that targets the receptors involved with cancer cell growth. The purpose of this study is to find out if Zanzalintinib is an effective treatment for participants with mCRPC with soft tissue or visceral metasteses who have progressed on prior ARPI treatments.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

19

Fase

  • Fase 2

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

Ubicaciones de estudio

    • Ohio
      • Cleveland, Ohio, Estados Unidos, 44106
        • University Hospitals Cleveland Medical Center, Case Comprehensive Cancer Center
        • Contacto:
        • Investigador principal:
          • Pedro Barata, MD, MSc

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 have histologically or cytologically confirmed metastatic castrate-resistant prostate cancer. Adenocarcinoma of prostate must be primary histology, but neuroendocrine features are allowed as long as <50% neuroendocrine histology. Tissue is not mandatory, but a pathologic report is required at time of participant enrollment.
  • Participants must have evidence of metastatic disease in soft tissue or visceral disease on conventional scans including CT and bone scans
  • Participants must have previously been treated with an ARPI (abiraterone, enzalutamide, apalutamide, darolutamide). Prior exposure to 1 line of taxane-based chemotherapy (docetaxel) is allowed.
  • Age ≥ 18 years.
  • Karnofsky Performance status ≥ 60%
  • Participants must have adequate organ and marrow function, based upon meeting all the following laboratory criteria within 14 days before first dose of study treatment as defined below:

    • Absolute neutrophil count (ANC) ≥ 1500/mm3 (≥ 1.5 GI/L) without granulocyte colony-stimulating factor support within 2 weeks of screening laboratory sample collection.
    • Platelets ≥ 100,000/mm3 (≥ 100 GI/L) without transfusion within 2 weeks of screening laboratory sample collection.
    • Hemoglobin ≥ 9 g/dL (≥ 90 g/L) without transfusion within 2 weeks prior to screening laboratory sample collection.
    • International Normalized Ratio (INR) ≤ 1.5 and activated partial thromboplastin time (aPTT) ≤ 1.2 x upper limit of normal (ULN).
    • Alanine aminotransferase (ALT), aspartate aminotransferase (AST), and alkaline phosphatase (ALP) ≤ 3 x ULN. For participants with documented bone metastasis ALP ≤ 5 x ULN. For participants with CRPC and bone metastasis ALP ≤ 10 x ULN if predominantly bone-specific ALP.
    • Total bilirubin ≤ 1.5 x ULN (for participants with Gilbert's disease ≤ 3 x ULN).
    • Serum creatinine ≤ 1.5 x ULN or calculated creatinine clearance ≥ 40 mL/min (≥ 0.67 mL/sec) using the Cockcroft Gault equation.
    • Urine protein-to-creatinine ratio (UPCR) ≤ 1 mg/mg (≤ 113.2 mg/mmol) creatinine.
  • Recovery to baseline or ≤ Grade 1 severity (CTCAE v5) from adverse events (AEs), including immune-related adverse events (irAEs), related to any prior treatments, unless AE(s) are clinically nonsignificant and/or stable on supportive therapy (eg, physiological replacement of corticosteroid). Low-grade or controlled toxicities such as alopecia, ≤ Grade 2 hypomagnesemia, ≤ Grade 2 neuropathy are permitted)
  • Participants must be capable of understanding and complying with the protocol requirements and must have signed the informed consent document.
  • Sexually active fertile participants and their partners must agree to use highly effective method of contraception (defined in Appendix III) during the course of the study and for the following durations after the last dose of treatment (whichever is later). An additional contraceptive method, such as a barrier method (eg, condom), is required. In addition, men must agree not to donate sperm and women must agree not to donate eggs (ova, oocyte) for the purpose of reproduction during these same periods:

    • through 186 days after the last dose of zanzalintinib for women of childbearing potential (WOCBP) or through 96 days after the last dose of zanzalintinib for men

Exclusion Criteria:

  • Evidence of hormone-sensitive prostate cancer (HSPC).
  • Evidence of small cell prostate cancer.
  • Prior treatment with any TKI (including zanzalintinib)
  • Receipt of any type of small molecule kinase inhibitor (including investigational kinase inhibitor) within 2 weeks before first dose of study treatment.
  • Receipt of any type of cytotoxic, biologic or other systemic anticancer therapy (including investigational) within 2 weeks before first dose of study treatment.

    • The antiandrogen abiraterone is permitted up to 1 week prior to first dose of study treatment. Concomitant use of megestrol acetate or leuprolide is permitted. Other types of hormonal therapies with similar use require prior approval from the Principal Investigator.
  • Another malignancy that requires active therapy and in the opinion of the Investigator would interfere with monitoring of radiologic assessments of response to Investigational Product, within 2 years before first dose of study treatment, except for superficial skin cancers, or localized, low-grade tumors deemed cured and not treated with systemic therapy.
  • Participants with BRCA-mutated mCRPC who have not previously received a PARP inhibitor
  • Participants with MSI-H mCRPC who have not previously received pembrolizumab or another immune-checkpoint inhibitor for treatment of MSI-H mCRPC
  • Radiation therapy for bone metastasis within 2 weeks, any other radiation therapy within 4 weeks before first dose of study treatment. Systemic treatment with radionuclides within 6 weeks before first dose of study treatment. Participants with clinically relevant ongoing complications from prior radiation therapy are not eligible.
  • Known brain metastases or cranial epidural disease unless adequately treated with radiotherapy and/or surgery (including radiosurgery) and stable for at least 4 weeks before first dose of study treatment. Note: Eligible participants must be neurologically asymptomatic and without corticosteroid treatment at the time of enrollment.

    • Base of skull lesions without definitive evidence of dural or brain parenchymal involvement are allowed.
  • Concomitant anticoagulation with oral anticoagulants (eg, warfarin, direct thrombin inhibitors ) and platelet inhibitors (eg, clopidogrel).

    • Allowed anticoagulants are the following:

      • Prophylactic use of low-dose aspirin for cardio-protection (per local applicable guidelines) and low-dose low molecular weight heparins (LMWH).
      • Therapeutic doses of LMWH or anticoagulation with direct factor Xa inhibitors rivaroxaban, edoxaban, or apixaban in participants without known brain metastases who are on a stable dose of the anticoagulant for at least 1 week before first dose of study treatment without clinically significant hemorrhagic complications from the anticoagulation regimen.

Note: Participants must have discontinued oral anticoagulants within 3 days or 5 half-lives prior to first dose of study treatment, whichever is longer.

  • The participant has uncontrolled, significant intercurrent or recent illness including, but not limited to, the following conditions:

    • Unstable or deteriorating cardiovascular disorders:
  • Congestive heart failure New York Heart Association Class 3 or 4, class 2 or higher, unstable angina pectoris, new-onset angina, serious cardiac arrhythmias (eg, ventricular flutter, ventricular fibrillation, Torsades de pointes).

    • Uncontrolled hypertension defined as sustained blood pressure (BP) > 140 mm Hg systolic or > 90 mm Hg diastolic despite optimal antihypertensive treatment.
    • Stroke (including transient ischemic attack [TIA]), myocardial infarction, or other clinically significant arterial thrombotic and/or ischemic event within 6 months before first dose of study treatment.
    • Pulmonary embolism (PE) or deep vein thrombosis (DVT) or prior clinically significant venous events within 3 months before first dose of study treatment.

      • Note: Participants with a diagnosis of DVT within 6 months are allowed if asymptomatic and stable at screening and are on a stable dose of the anticoagulant for at least 1 week before first dose of study treatment without clinically significant hemorrhagic complications from the anticoagulation regimen.
      • Note: Participants who don't require prior anticoagulation therapy may be eligible but must be discussed and approved by the Principal Investigator.

        • Gastrointestinal (GI) disorders including those associated with a high risk of perforation or fistula formation:
    • Tumors invading the GI-tract from external viscera
    • Active peptic ulcer disease, inflammatory bowel disease, diverticulitis, cholecystitis, symptomatic cholangitis or appendicitis, or acute pancreatitis
    • Acute obstruction of the bowel, gastric outlet, or pancreatic or biliary duct within 6 months before first dose unless cause of obstruction is definitively managed and participant is asymptomatic
    • Abdominal fistula, gastrointestinal perforation, bowel obstruction, or intra-abdominal abscess within 6 months before first dose. Note: Complete healing of an intra-abdominal abscess must be confirmed before first dose of study treatment.
    • Known gastric or esophageal varices
    • Ascites, pleural effusion, or pericardial fluid requiring drainage in last 4 weeks
  • Clinically significant hematuria, hematemesis, or hemoptysis of > 0.5 teaspoon (2.5 ml) of red blood, or other history of significant bleeding (eg, pulmonary hemorrhage) within 12 weeks before first dose of study treatment.
  • Symptomatic cavitating pulmonary lesion(s) or endobronchial disease (asymptomatic or radiated lesions allowed)
  • Lesions invading major blood vessel including, but not limited to, inferior vena cava, pulmonary artery, or aorta. Note: Participants with intravascular tumor extension may be eligible following Principal Investigator approval.
  • Other clinically significant disorders that would preclude safe study participation:

    • Active infection requiring systemic treatment.

      • Note: Prophylactic antimicrobial treatments (antibiotics, antimycotic, antiviral) are allowed.
    • Known infection with acute or chronic hepatitis B or C, known human immunodeficiency virus (HIV) or acquired immunodeficiency syndrome (AIDS)-related illness except for participants meeting all of the following criteria: (1) on stable anti-retroviral therapy; (2) CD4+ T cell count ≥ 200/µL; and (3) an undetectable viral load.

      • Note: HIV testing will be performed at screening if and as required by local regulation.
      • Note: To be eligible, participants taking CYP inhibitors (eg, zidovudine, ritonavir, cobicistat, didanosine) or CYP3 inducers (efavirenz) must change to a different regimen not including these drugs 7 days prior to initiation of study treatment. Anti-retroviral therapies (ART) must have been received for at least 4 weeks prior to the first dose.
      • Note: CD4+ T cell counts, and viral load are monitored per standard of care by the local health care provider.
    • Serious non-healing wound/ulcer/bone fracture.

      • Note: non-healing wounds or ulcers are permitted if due to tumor-associated skin lesions.
    • Malabsorption syndrome.
    • Pharmacologically uncompensated, symptomatic hypothyroidism.
    • Moderate to severe hepatic impairment (Child-Pugh B or C).
    • Requirement for hemodialysis or peritoneal dialysis.
    • History of solid organ or allogeneic stem cell transplant.
  • Major surgery (as defined in Appendix IV; eg, GI surgery, removal or biopsy of brain metastasis) within 8 weeks prior to first dose of study treatment. Prior laparoscopic surgeries (ie nephrectomy) within 4 weeks prior to first dose of study treatment. Minor surgery (eg, simple excision, tooth extraction) within 5 days before first dose of study treatment. Complete wound healing from major or minor surgery must have occurred at least prior to first dose of study treatment.

    • Note: Fresh tumor biopsies should be performed at least 5 days before the first dose of study treatment. Participants with clinically relevant ongoing complications from prior surgical procedures, including biopsies, are not eligible.
  • Corrected QT interval calculated by the Fridericia formula (QTcF) > 480 ms within 14 days per electrocardiogram (ECG) before first dose of study treatment.

    • Note: Triplicate ECG evaluations will be performed and the average of these 3 consecutive results for QTcF will be used to determine eligibility.
  • History of psychiatric illness likely to interfere with ability to comply with protocol requirements or give informed consent.
  • Inability to swallow tablets.
  • Previously identified allergy or hypersensitivity to components of the study treatment formulations.
  • Other conditions, which in the opinion of the Investigator, would compromise the safety of the participant or the participant's ability to complete the study.
  • Prior treatment toxicities not resolved to ≤ Grade 2 according to the NCI CTCAE Version 5.0.

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: Zanzalintiniib
Single-arm phase 2 trial of patients with mCRPC (metastatic castration-resistant prostate cancer). About 24 participants will be enrolled in the trial, 9 will initially be enrolled and if 3 participants are still alive and progression-free at 6 months, 15 more participants will be added. 1 cycle is 28 days. If a participant does not complete at least one cycle, the participant will be replaced. Participants who complete one cycle will not be replaced.
60mg zanzalinitib will be given daily starting on Cycle 1 Day 1 until disease progression or unacceptable toxicity

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Radiographic progression free survival (rPFS) at 6 months
Periodo de tiempo: 6 months
rPFS is defined as the duration of time from start of treatment to time of progression
6 months

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Prostate specific antigen (PSA) response
Periodo de tiempo: 6 months
PSA response is defined as the rate that patients achieve PSA decline of greater than or equal to 50% (PSA50). PSA decline will be measured by determining the ratio to PSA obtained on cycle 5 day 1 to baseline PSA obtained cycle 1 day 1.
6 months
Time to next systemic treatment
Periodo de tiempo: 24 months
Time to next systemic treatment is measured in months from the day of treatment initiation on this study (cycle 1 day 1) to the first day of subsequent systemic cancer-directed therapy.
24 months
Median progression free survival
Periodo de tiempo: 24 months
Median progression free survival is determined by Prostate Cancer Clinical Trials Working Group (PCWG3) response criteria, which incorporates PSA and imaging. For PSA, PCWG3 defines PSA progression as an increase in PSA greater than 25% and >2 ng/mL above the nadir. For imaging, RECIST version 1.1 will be used to asses the lymph nodes and solid organ disease.
24 months
Overall Survival (OS)
Periodo de tiempo: 24 months
Overall survival is defined as the time from start of treatment (cycle 1, day 1) until death from any cause (cancer-related or not)
24 months
Objective Response Rate (ORR)
Periodo de tiempo: 24 months
Objective response rate is defined as the percentage of treated patients who achieve either a complete response (CR) or partial response (PR) as their best overall response, as assessed on cross-sectional imaging according to Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1.
24 months

Colaboradores e Investigadores

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

Patrocinador

Investigadores

  • Investigador principal: Pedro Barata, MD, MSc, University Hospitals Cleveland Medical Center, Case Comprehensive Cancer Center

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)

1 de octubre de 2026

Finalización primaria (Estimado)

1 de mayo de 2029

Finalización del estudio (Estimado)

1 de mayo de 2030

Fechas de registro del estudio

Enviado por primera vez

20 de mayo de 2026

Primero enviado que cumplió con los criterios de control de calidad

20 de mayo de 2026

Publicado por primera vez (Actual)

27 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

16 de septiembre de 2026

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

14 de septiembre de 2026

Última verificación

1 de septiembre de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • CASE6825

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

SÍ

Marco de tiempo para compartir IPD

Data included in the peer-reviewed publication will be publicly available indefinitely. No raw data will be shared

Criterios de acceso compartido de IPD

A peer-reviewed publication will be made available according to the publishing journal's specifications. UH personnel will not share study data apart that which has been published publicly.

Tipo de información de apoyo para compartir IPD

  • PROTOCOLO DE ESTUDIO
  • SAVIA
  • CIF
  • RSC

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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