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Neoadjuvant Avutometinib/Defactinib and mFOLFIRINOX Combination Therapy in Pancreatic Adenocarcinoma (Panc 004)

11 september 2026 uppdaterad av: Matthew Reilley, University of Virginia

Neoadjuvant Avutometinib/Defactinib and mFOLFIRINOX Combination Therapy in Pancreatic Adenocarcinoma: A Phase IB/II Safety and Efficacy Study

The goal of this study is to find out if taking two oral study drugs (avutometinib and defactinib) are safe for patients with pancreatic ductal adenocarcinoma (PDAC). Researchers also want to see if the drugs can slow down tumor growth and shrink tumors for possible surgery. These drugs are approved by the FDA to treat a certain kind of ovarian cancer. This study has two parts:

  • Part A is for patients whose cancer has spread to other parts of the body.
  • Part B is for patients whose cancer has not spread, but who cannot have surgery.

Participants will take both drugs as told by their doctor with their regular cancer medicine. Participants will also give blood samples throughout the study. These samples will help researchers learn about how participants respond to treatment and about their pancreatic cancer.

Studieöversikt

Detaljerad beskrivning

Participants in part A will take the study drugs in 28-day cycles for up to 6 cycles with their chemotherapy. Participants whose cancer is not getting worse (known as disease control) may continue the study drugs in combination with maintenance chemotherapy until their disease worsens or negative side effects are noted.

Participants in part B will take the study drugs in 28-day cycles for up to 6 cycles with their chemotherapy. After cycle 4 and cycle 6, participants will have their disease re-assessed with consideration for surgery. Participants whose cancer is not getting worse (disease control) but are ineligible for surgery may continue the study drugs in combination with maintenance chemotherapy until their disease worsens or negative side effects are noted.

Studietyp

Interventionell

Inskrivning (Beräknad)

31

Fas

  • Fas 2
  • Fas 1

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

Studera Kontakt Backup

Studieorter

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Vuxen
  • Äldre vuxen

Tar emot friska volontärer

Nej

Beskrivning

Inclusion Criteria:

  1. Provision of signed and dated informed consent form.
  2. Individuals ≥ 18 years of age.
  3. Stated willingness to comply with all study procedures and availability for the duration of the study.
  4. Ability to take oral medication and be willing to adhere to the study intervention regimen.
  5. Ability to receive mFOLFIRINOX.
  6. Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.
  7. Adenocarcinoma of the pancreas, confirmed by histology or cytology.

    1. Part A: Metastatic pancreatic cancer
    2. Part B: Borderline resectable or locally advanced PDAC not eligible for primary surgical resection per institutional standards and following a multidisciplinary discussion at local tumor board
  8. No prior systemic or localized treatment for PDAC.
  9. Radiographically measurable disease of at least one site by computed tomography (CT) or magnetic resonance (MR) imaging, as defined by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1.
  10. Individuals must have adequate organ function defined by the following laboratory parameters:

    Absolute neutrophil count (ANC): ≥ 1500/mm3 Platelets: ≥100,000/mm3 Hemoglobin: ≥9 g/dL Serum Creatinine: ≤ 1.5 x ULN or creatinine clearance rate of ≥ 50 mL/min as calculated by the Cockcroft-Gault formula Bilirubin: ≤ 1.5 x ULN (except in patients with Gilbert's disease, where bilirubin to 3x ULN is allowed).

    AST and ALT: ≤ 2.5 x ULN or ≤ 5 x ULN for patients with liver metastasis INR: ≤ 1.5 x ULN in the absence of anticoagulation or therapeutic levels in the presence of anticoagulation Creatine phosphokinase (CPK): ≤ 2.5 x ULN

  11. Baseline corrected QT interval (QTc) interval ≤ 480 millisecond (ms) (CTCAE v5.0, Grade 0-1) using Fridericia's QT correction formula.

    • Patients with a left bundle branch block (LBBB) > 480 ms will need their QTc calculated by Bazett (QTc = QT(measured) - 0.5 × QRS(LBBB)).

Exclusion Criteria:

  1. Patients with pancreatic neuroendocrine tumors (PNET), islet cell tumors, mucinous cystic, acinar or squamous (≥ 50%) histology are excluded.
  2. Prior treatment for pancreatic ductal adenocarcinoma.
  3. Presence of distant metastases (Part B only).
  4. Presence of symptomatic ascites or the need for paracentesis within 2 weeks prior to registration.
  5. Major surgery within 4 weeks (excluding placement of vascular access) of registration.
  6. Patients with a prior or concurrent malignancy within past 5 years whose natural history or treatment has the potential to interfere with the safety or efficacy assessment of the investigational regimen. Examples of malignancies that may be permitted include non-melanoma skin cancer, localized prostate cancer treated with curative intent or under active surveillance, localized thyroid cancer (papillary or follicular), non-muscle invasive low-grade bladder cancer, resected gastrointestinal stromal tumor, stage I testicular cancer post orchiectomy, WHO (World Health Organization) grade 1 meningioma.
  7. Prior treatment with either inhibitors of the RAS/MAPK pathway [e.g., MEK inhibitors] or inhibitors of FAK within the last 6 months.
  8. Patients on treatment with warfarin within 5 days of registration. Patients on warfarin for deep vein thrombosis or pulmonary embolism can be converted to low-molecular-weight heparin or direct oral anticoagulants (DOACs).
  9. Participants requiring medications or supplements with potential for drug-drug interactions, specifically strong CYP3A4 or CYP2C9 inhibitors or inducers (Table 7). Participants must be off these medications for 7 days prior to the first dose of study intervention(s). These substances should also be avoided during the course of therapy.
  10. Patients with known UGT1A1 deficiency based on genetic analysis of the UGT1A1 gene.
  11. Receipt of live vaccines (not limited to the following: measles, mumps, rubella, chicken pox, yellow fever, rabies, BCG) within 30 days of registration. Seasonal influenza vaccines for injection are generally killed virus vaccines and are permitted. However, intranasal influenza vaccines (e.g., FluMist®) are live attenuated vaccines and are not permitted.
  12. Active, uncontrolled bacterial, viral, or fungal infection(s) requiring systemic therapy.
  13. Active Human Immunodeficiency Virus (HIV) infection, unless patient is on effective anti-retroviral therapy and was shown to have a negative viral load within 6 months of registration.
  14. Active Hepatitis B Virus (HBV) or Hepatitis C (HCV) infection, unless patient is on antiviral therapy and was shown to have a negative viral load test within 6 months of registration.
  15. Active skin disorder that requires current systemic therapy.
  16. Concurrent ocular disorders:

    • Patients with history of glaucoma or history of retinal vein occlusion (RVO).
    • Patients with history of retinal pathology or evidence of visible retinal pathology that is considered a risk factor for RVO.
    • Patients with active or chronic, visually significant corneal disorders, other active ocular conditions requiring ongoing therapy that prevent adequate monitoring of drug-induced keratopathy. Examples of visually significant corneal disorders include corneal degeneration, active or recurrent keratitis, and other forms of serious ocular surface inflammatory conditions. Visually significant corneal disorders do NOT include dry eyes, blepharitis, and uncomplicated corneal erosions.
  17. Patients with history of interstitial lung disease (ILD) or pulmonary fibrosis.
  18. Patients with history of severe obstructive pulmonary disease on long-term, home oxygen.
  19. Patients with congestive heart failure III/ IV cardiac disease (New York Heart Association [NYHA]), myocardial infarction within the last 6 months, unstable arrhythmias or unstable angina.
  20. Patients receiving immunosuppressive or myelosuppressive medications that, in the opinion of the investigator, would increase the risk of serious neutropenic complications. Subjects receiving replacement therapy of ≤10 mg of prednisone (or the equivalent hydrocortisone dose) per day are eligible.
  21. History of prior allogeneic stem cell or solid organ transplantation.
  22. Patients with impaired gastrointestinal absorption due to gastrectomy or active inflammatory bowel disease.
  23. Patients with pre-existing peripheral neuropathy of CTCAE Grade ≥2 (severe symptoms limiting self-care ADL (activity of daily living)).
  24. Patients with a history of allergy or known hypersensitivity to any of the study treatments or any of their excipients as outlined in the respective package insert.
  25. Individuals with reproductive potential who do not agree to use highly effective method of contraceptive as described in Lifestyle Considerations (sections 5.4.2 and 5.4.3).
  26. Patients who are pregnant or breastfeeding.
  27. Treatment with another investigational drug during the study participation.
  28. Any other medical condition, related to the underlying disease (e.g., cardiac, gastrointestinal, pulmonary, psychiatric, neurological) that in the opinion of the investigator would place the patient at unacceptably high risk for toxicity.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: N/A
  • Interventionsmodell: Sekventiell tilldelning
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: Neoadjuvant avutometinib + defactinib with standard of care chemotherapy
Avutometinib and defactinib will be taken for 3 weeks, followed by a 1-week rest period in each 4 week cycle.
Participants will receive avutometinib and defactinib in combination with mFOLFIRINOX (standard of care chemotherapy) in 28-day cycles for up to 6 cycles.

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Dose limiting toxicities (DLTs) - Part A
Tidsram: 1 cycle (28 days)
For each participant, we will determine DLTs during first cycle of neoadjuvant therapy
1 cycle (28 days)
Objective response (OR) - Part B
Tidsram: through 6 cycles (each cycle is 28 days)
PR (partial response) or CR (complete response) per RECIST criteria
through 6 cycles (each cycle is 28 days)

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
TRAEs (Treatment-related adverse events)
Tidsram: Up to 30 days after completion of study treatment (average of 6 months)
Cumulative incidence of adverse events as defined by CTCAE v5 tabulating frequency, proportion, and severity
Up to 30 days after completion of study treatment (average of 6 months)
(Part B only): Surgical resection rate
Tidsram: after all participants complete up to 6 cycles (each cycle is 28 days)
We will determine the number of participants eligible for surgical resection out the total number of study participants.
after all participants complete up to 6 cycles (each cycle is 28 days)
EFS (event free-survival)
Tidsram: through study completion (an average of a year)
disease progression, disease recurrence after surgery, or death
through study completion (an average of a year)

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Samarbetspartners

Utredare

  • Huvudutredare: Matthew Reilley, MD, University of Virginia

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Beräknad)

1 oktober 2026

Primärt slutförande (Beräknad)

1 april 2029

Avslutad studie (Beräknad)

1 april 2030

Studieregistreringsdatum

Först inskickad

2 september 2026

Först inskickad som uppfyllde QC-kriterierna

11 september 2026

Första postat (Faktisk)

17 september 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

17 september 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

11 september 2026

Senast verifierad

1 september 2026

Mer information

Termer relaterade till denna studie

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Ja

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

produkt tillverkad i och exporterad från U.S.A.

Nej

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