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

14 settembre 2026 aggiornato da: 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.

Panoramica dello studio

Descrizione dettagliata

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 di studio

Interventistico

Iscrizione (Stimato)

30

Fase

  • Fase 1

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Luoghi di studio

    • Oklahoma
      • Oklahoma City, Oklahoma, Stati Uniti, 73104
        • University of Oklahoma Health Campus
        • Contatto:

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

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

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Comparatore attivo: 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
Sperimentale: 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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Number and proportion of patients with Grade 3 and higher adverse events deemed related to pentamidine during trial treatment, using CTCAE v.6.0.
Lasso di tempo: 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

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Evaluation of the objective response rate in modified FOLFIRINOX (arm A) versus modified FOLFIRINOX plus Pentamidine (arm B)
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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.
Lasso di tempo: 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

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Susanna Ulahannan, MD, University of Oklahoma

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 dicembre 2026

Completamento primario (Stimato)

1 dicembre 2029

Completamento dello studio (Stimato)

1 dicembre 2030

Date di iscrizione allo studio

Primo inviato

14 settembre 2026

Primo inviato che soddisfa i criteri di controllo qualità

14 settembre 2026

Primo Inserito (Effettivo)

18 settembre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

18 settembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

14 settembre 2026

Ultimo verificato

1 settembre 2026

Maggiori informazioni

Termini relativi a questo studio

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

Sì

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

prodotto fabbricato ed esportato dagli Stati Uniti

Sì

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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