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Modified FOLFIRINOX and Pentamidine in Advanced and Metastatic Pancreatic Cancer (FALCON)

14 de septiembre de 2026 actualizado por: University of Oklahoma

Modified FOLFIRINOX and Pentamidine as First-line Treatment in Advanced and Metastatic Pancreatic Ductal Adenocarcinoma

The purpose of this research is to observe the effects of using a new combination of drugs to inhibit tumor growth.

Descripción general del estudio

Descripción detallada

The patients will undergo testing, exams, and procedures per the Protocol. On study, patients will be randomized into one of the two arms. In Arm A (up to 15 patients) will be treated with modified FOLFIRINOX every two weeks, delivered as follows:

  • Oxaliplatin 85mg/m2 IV over 2 hours on Day 1, followed by,
  • Irinotecan 150mg/m2 IV over 90 minutes on Day 1, followed by
  • Leucovorin 400mg/m2 IV over 2 hours on Day 1, followed by
  • 5FU 2400mg/m2 IV over 46-48 hours on Days 1-3

In arm B patients (up to 15), the same modified FOLFIRINOX regimen will be used, as above, plus 300 mg pentamidine will be administered IV over a one-hour infusion on Day 1 of each cycle.

In both arms, patients will be treated over eight two-week cycles, and the entire treatment is expected to last approximately 4 months.

After eight cycles, patients will undergo another EUS core biopsy. At the same time as the biopsy, an additional blood draw (for translational endpoints) will be done.

After the biopsy, patients will continue treatment per physician's discretion for an additional 2 months (or 4 cycles) for a total of 12 cycles (or 6 months of treatment) until disease progression or appearance of unacceptable toxicity.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

30

Fase

  • 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

Copia de seguridad de contactos de estudio

Ubicaciones de estudio

    • Oklahoma
      • Oklahoma City, Oklahoma, Estados Unidos, 73104
        • University of Oklahoma Health Campus
        • 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:

  • Written informed consent signed and dated by the patient
  • At least 18 years-of-age at the time of signature of the informed consent form (ICF)
  • Eastern Cooperative Oncology Group (ECOG) Performance Status score of 0 or 1
  • Patients with a confirmed diagnosis of locally advanced, unresectable and/or metastatic pancreatic cancer
  • Patients must have at least one measurable disease per RECIST v1.1,
  • Patients must have at least 1 tumor lesion amenable to biopsy and must be willing to undergo a biopsy prior to first treatment and after receiving 8th cycle of therapy.
  • Adequate bone marrow function defined as ANC> 1000/μL and platelets>75,000/μL
  • Adequate liver function defined as total bilirubin<1.5g/L
  • Adequate renal function defined as creatinine <1.5ULN or creatinine clearance greater than 30 ml/m2.
  • AST and ALT <2.5x ULN or AST and ALT<5xULN if liver function abnormalities are due to liver metastases
  • Male or female patients. Male patients with female partners of childbearing potential and female patients of childbearing potential are required to use two forms of acceptable contraception, including one barrier method, during their participation in the study and for 30 days following the last dose. Male patients must also refrain from donating sperm during their participation in the study.
  • Life expectancy ≥ 3 months according to the Investigator's judgment.

Exclusion Criteria:

  • Any systemic anti-cancer chemotherapy, small molecule, biologic, or from a previous treatment regimen or clinical study in a metastatic setting before the first dose of study drug.
  • Active bacterial infection
  • Women who are pregnant, nursing, or who plan to become pregnant while in the study and for at least 6 months after the last administration of study treatment
  • Men who plan to father a child while in the study and for at least 6 months after the last administration of study treatment
  • Any of the following cardiac criteria currently or within the last 6 months:

    1. Mean resting corrected QT interval (QTc) >480 msec
    2. Any clinically important abnormalities (as assessed by the Investigator) in rhythm, conduction, or morphology of resting electrocardiograms (ECGs), e.g., complete left bundle branch block, third degree heart block
    3. Congestive heart failure (New York Heart Association ≥ Grade 2
    4. Any factors that increase the risk of QTc prolongation or risk of arrhythmic events such as heart failure, hypokalemia, congenital long QT syndrome, family history of long QT syndrome or unexplained sudden death under 40 years-of-age, or any concomitant medication known to prolong the QT interval
  • Incidences of chronic hypokalemia that cannot be corrected.
  • As judged by the Investigator, any evidence of severe or uncontrolled systemic diseases, including uncontrolled hypertension, uncontrolled diabetes mellitus, active bleeding diatheses, or active infection requiring treatment including hepatitis B, hepatitis C, and human immunodeficiency virus. Screening for chronic conditions is not required.
  • Presence of other active invasive cancers other than the one treated in this study within 2 years prior to screening, except appropriately treated basal cell carcinoma of the skin, or in situ carcinoma of uterine cervix, or other local tumors considered cured by local treatment
  • Psychological, familial, sociological, or geographical conditions that do not permit compliance with the protocol and/or follow-up procedures outlined in the protocol.
  • Prisoners

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: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Comparador activo: modified FOLFIRINOX

In Arm A (up to 15 patients) will be treated with modified FOLFIRINOX every two weeks, delivered as follows:

  • Oxaliplatin 85mg/m2 IV over 2 hours on Day 1, followed by,
  • Irinotecan 150mg/m2 IV over 90 minutes on Day 1, followed by
  • Leucovorin 400mg/m2 IV over 2 hours on Day 1, followed by
  • 5FU 2400mg/m2 IV over 46-48 hours on Days 1-3

Patients will be treated over eight two-week cycles, and the entire treatment is expected to last approximately 4 months.

In Arm A (up to 15 patients) will be treated with modified FOLFIRINOX every two weeks, delivered as follows:

  • Oxaliplatin 85mg/m2 IV over 2 hours on Day 1, followed by,
  • Irinotecan 150mg/m2 IV over 90 minutes on Day 1, followed by
  • Leucovorin 400mg/m2 IV over 2 hours on Day 1, followed by
  • 5FU 2400mg/m2 IV over 46-48 hours on Days 1-3
Experimental: modified FOLFIRINOX + Pentamidine

In arm B patients (up to 15), the same modified FOLFIRINOX regimen will be used, as above, plus 300 mg pentamidine will be administered IV over a one-hour infusion on Day 1 of each cycle.

Patients will be treated over eight two-week cycles, and the entire treatment is expected to last approximately 4 months.

In Arm A (up to 15 patients) will be treated with modified FOLFIRINOX every two weeks, delivered as follows:

  • Oxaliplatin 85mg/m2 IV over 2 hours on Day 1, followed by,
  • Irinotecan 150mg/m2 IV over 90 minutes on Day 1, followed by
  • Leucovorin 400mg/m2 IV over 2 hours on Day 1, followed by
  • 5FU 2400mg/m2 IV over 46-48 hours on Days 1-3
In arm B patients (up to 15), the same modified FOLFIRINOX regimen will be used, as above, plus 300 mg pentamidine will be administered IV over a one-hour infusion on Day 1 of each cycle.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Number and proportion of patients with Grade 3 and higher adverse events deemed related to pentamidine during trial treatment, using CTCAE v.6.0.
Periodo de tiempo: 3 years
To evaluate the safety in patients with metastatic or nonresectable locally advanced pancreatic cancer treated with modified FOLFIRINOX (arm A) versus modified FOLFIRINOX plus Pentamidine (arm B)
3 years

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Evaluation of the objective response rate in modified FOLFIRINOX (arm A) versus modified FOLFIRINOX plus Pentamidine (arm B)
Periodo de tiempo: 3 years
Proportion of patients with Objective response rate and partial response as measured by RECIST version 1.1 to be evaluated by imaging study and radiology review.
3 years
Evaluation of the rate of progression-free survival in both arms
Periodo de tiempo: 3 years
Proportion of patients with a response rate measurement of Progression-free survival determined by the number of days from the start of study treatment to date of imaging-confirmed tumor progression, death or last time of follow up
3 years
Evaluation of the duration of response in both arms
Periodo de tiempo: 3 years
Proportion of patients with Duration of response determined as the number of days from the onset of the first response to disease progression or death
3 years
Evaluation of genetic mutations that predict patient response to modified FOLFIRINOX plus Pentamidine
Periodo de tiempo: 3 years
Proportion of patients with expression levels of MUC1, SAT1, and other metabolic genes by performing transcriptomic analysis of biopsies.
3 years
Evaluation of potential utility of N1-acetylspermidine and nucleotide pools as a biomarker of efficacy of the combination therapy.
Periodo de tiempo: 3 years
Proportion of patients with circulating N'acetylspermidine1levels, other circulating polyamines levels, tumor tissue uptake of pentamidine by quantitating N1-acetylspermidine levels by liquid chromatography-coupled tandem mass spectrometry, and quantitate nucleotide pools in biopsy tissues by liquid chromatography-coupled tandem mass spectrometry
3 years

Colaboradores e Investigadores

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

Patrocinador

Investigadores

  • Investigador principal: Susanna Ulahannan, MD, University of Oklahoma

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 diciembre de 2026

Finalización primaria (Estimado)

1 de diciembre de 2029

Finalización del estudio (Estimado)

1 de diciembre de 2030

Fechas de registro del estudio

Enviado por primera vez

14 de septiembre de 2026

Primero enviado que cumplió con los criterios de control de calidad

14 de septiembre de 2026

Publicado por primera vez (Actual)

18 de septiembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

18 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

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

producto fabricado y exportado desde los EE. UU.

Sí

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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