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Testing Pasritamig Before Surgery for the Treatment of Localized Prostate Cancer

1 października 2026 zaktualizowane przez: Fred Hutchinson Cancer Center

A Neoadjuvant Trial of Pasritamig in Unfavorable Intermediate to Very High-Risk Localized Prostate Cancer

This phase I trial tests the safety and feasibility of giving pasritamig before surgery in patients with unfavorable intermediate-risk, high-risk, or very high-risk localized prostate cancer. Pasritamig is a bispecific antibody that works by bringing immune cells called T cells close to prostate cancer cells that express KLK2, which may help the immune system attack the cancer. Giving pasritamig before radical prostatectomy may help researchers determine how the drug affects prostate cancer and the immune cells within the tumor.

Przegląd badań

Status

Jeszcze nie rekrutacja

Warunki

Interwencja / Leczenie

Typ studiów

Interwencyjne

Zapisy (Szacowany)

18

Faza

  • Faza 1

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Kontakt w sprawie studiów

Lokalizacje studiów

    • Washington
      • Seattle, Washington, Stany Zjednoczone, 98109
        • Fred Hutch/University of Washington Cancer Consortium
        • Kontakt:
        • Główny śledczy:
          • Steven Blinka, MD, PhD

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

18 lat i starsze (Dorosły, Starszy dorosły)

Akceptuje zdrowych ochotników

Nie

Płeć kwalifikująca się do nauki

Męski

Opis

Inclusion Criteria:

  • Must be willing to provide informed consent prior to any study specific procedures.

  • Age ≥ 18 years.

  • Documented histologically confirmed adenocarcinoma of the prostate:

    • Unfavourable intermediate risk:

      --- Grade Group 1 with PSA 10-20 ng/mL, T2b-T2c OR Grade Group 2 with PSA 10-20 ng/mL, T2b-T2c, and/or ≥50% biopsy cores positive OR Grade Group 3 with PSA <20 ng/mL.

    • High-risk localized prostate cancer with no very-high-risk features and exactly one high-risk feature:

      • T3a OR
      • Grade Group 4 or 5 OR
      • PSA > 20 ng/dL
    • Very high-risk localized prostate cancer. At least one of the following:

      • T3b-T4
      • Primary Gleason pattern 5
      • 2 or 3 high-risk features
      • >4 cores with Grade Group 4 or 5
  • Negative for distant metastases on conventional (i.e. CT bone scan) and PSMA PET imaging within 60 days of enrollment. Patients with evidence of non-measurable (i.e. per RECIST v1.1) metastatic lymphadenopathy as detected by PSMA PET will be eligible if ≤3 radiation isocenters are detectable.

  • Eastern cooperative oncology group performance (ECOG) status 0-1.

  • Eligible and planned for radical prostatectomy.

  • Must have adequate archival biopsy tissue available for KLK2 assessment.

  • Participants who are sexually active with a partner of childbearing potential or a pregnant partner must agree to use contraception, including a condom, during study treatment and for at least 6 months after the last dose of pasritamig. Participants must also agree not to donate sperm during study treatment and for at least 6 months after the last dose of pasritamig.

  • Patients must have normal organ and bone marrow function measured within 28 days prior to administration of study treatment as defined below:

    • Hemoglobin ≥ 9 g/dL with no blood transfusion in the past 28 days

    • Absolute neutrophil count (ANC) ≥1.5 × 10⁹/L; however, participants with documented Duffy-null associated neutrophil count or other benign chronic neutropenia may be eligible with ANC ≥1.0 × 10⁹/L if clinically stable and without a history of recurrent or severe infections, at the discretion of the investigator. Platelet count ≥ 100 x 109/L

    • Total bilirubin ≤1.5 × institutional upper limit of normal (ULN), except participants with known or suspected Gilbert syndrome may be eligible with total bilirubin ≤3 × ULN, provided direct bilirubin is ≤1.5 × ULN and there is no clinical evidence of hepatic dysfunction.Aspartate aminotransferase (AST) (Serum Glutamic Oxaloacetic Transaminase (SGOT)) / Alanine aminotransferase (ALT) (Serum Glutamic Pyruvate Transaminase (SGPT)) ≤ 2.5 x institutional upper limit of normal unless liver metastases are present in which case they must be ≤ 5x ULN

    • Patients must have creatinine clearance estimated of ≥30 mL/min:

      • Estimated creatinine clearance = (140-age [years]) x weight (kg) / serum creatinine (mg/dL) x 72

Exclusion Criteria:

  • Subjects with small cell or neuroendocrine prostate cancer.

  • Active infection or condition that requires treatment with systemic antibiotics within 7 days prior to the first dose of study treatment. Prophylactic anti-infective agents are allowed.

  • Solid organ or bone marrow transplantation.

  • Suspected or known allergies, hypersensitivity, or intolerance to excipients of pasritamig (refer to the latest IB for pasritamig).

  • Received immunosuppressive doses of systemic medications, such as glucocorticoids (doses >10 mg/day prednisone or equivalent) within 3 days prior to the first dose of study treatment. A single course of glucocorticoids is permitted as prophylaxis for imaging contrast (i.e., for participants with allergies to contrast). If glucocorticoids were used to treat immune-related adverse events associated with prior therapy, ≥7 days must have elapsed since the last dose of corticosteroid.

  • Received or plans to receive any live, attenuated vaccine within 4 weeks before the first dose of study treatment. Live, attenuated influenza vaccines are permitted as late as 7 days before the study treatment.

  • Distant metastasis based on conventional imaging (clinical stage M1) and PSMA PET within 60 days of enrollment. Nodal disease below the iliac bifurcation (clinical stage N1) is not an exclusion. Diagnosis of distant metastasis (clinical M stage; M0 versus M1a, M1b, M1c) and pelvic nodal disease (clinical N stage; N1 versus N0) will be assessed by central radiological review. Participants are considered eligible only if the central radiological review confirms clinical stage M0. As noted above, non-measurable nodal metastases detected on PSMA PET will be allowed to enroll if radiation isocenters are detectable.

  • cT4 disease (tumor is fixed or invades adjacent structures other than seminal vesicles) is excluded.

  • Prior androgen deprivation therapy or other systemic treatment for prostate cancer.

  • Prior treatment with KLK2-targeted therapy and/or with any CD3-directed therapy

  • Patients considered a poor medical risk due to a serious, uncontrolled medical disorder, non-malignant systemic disease or active, uncontrolled infection. This includes, but not limited to, the following:

    • Patients with positive HIV titers or active hepatitis (i.e., Hepatitis B or C) due to risk of transmitting the infection through blood or other body fluids.
    • Evidence of serious and/or unstable pre-existing medical, psychiatric or other condition (including laboratory abnormalities) that could interfere with patient safety or provision of informed consent to participate in this study.
    • Any psychological, familial, sociological, or geographical condition that could potentially interfere with compliance with the study protocol and follow-up schedule.
  • Any of the following within 6 months prior to first dose of study treatment:

    • Myocardial infarction,
    • Severe or unstable angina,
    • Clinically significant ventricular arrhythmias,
    • Congestive heart failure (New York Heart Association class II to IV),
    • Transient ischemic attack,
    • Cerebrovascular accident
  • Active autoimmune disease within the 12 months prior to signing consent that requires systemic immunosuppressive medications (e.g., chronic corticosteroid, methotrexate, or tacrolimus).

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Nie dotyczy
  • Model interwencyjny: Zadanie dla jednej grupy
  • Maskowanie: Brak (otwarta etykieta)

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: Neoadjuvant Pasritamig

Participants receive pasritamig IV on days 1, 8, 15, and 57. Participants then undergo standard of care radical prostatectomy. Participants also undergo blood and tissue sample collection on study.

Given IV

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Feasibility of neoadjuvant pasritamig
Ramy czasowe: From first dose through radical prostatectomy, approximately 70 days

Proportion of participants who complete planned neoadjuvant pasritamig and undergo radical prostatectomy within the protocol-defined surgical window without treatment-related delay.

From first dose through radical prostatectomy, approximately 70 days
Change in intratumoral CD3+ T-cell density
Ramy czasowe: Baseline to radical prostatectomy, approximately 70 days

Measured as CD3-positive T cells per mm² of evaluable tumor area

Baseline to radical prostatectomy, approximately 70 days

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Adverse pathologic features
Ramy czasowe: At radical prostatectomy, approximately Day 70

Number and proportion of evaluable participants with extraprostatic extension (≥ypT3a), seminal vesicle invasion (ypT3b), regional lymph node involvement (ypN1), positive surgical margins, and any adverse pathologic feature.

At radical prostatectomy, approximately Day 70
Change in prostate-specific antigen (PSA)
Ramy czasowe: Screening through approximately 12 weeks following radical prostatectomy
Screening through approximately 12 weeks following radical prostatectomy
Time to biochemical recurrence or death
Ramy czasowe: From radical prostatectomy through up to 3 years of follow-up

Time from radical prostatectomy to biochemical recurrence or death, whichever occurs first. Biochemical recurrence is defined as postoperative PSA ≥0.2 ng/mL, confirmed by a second PSA ≥0.2 ng/mL when clinically feasible.

From radical prostatectomy through up to 3 years of follow-up
Pathologic complete response (pCR)
Ramy czasowe: At radical prostatectomy, approximately Day 70

Proportion of evaluable participants with no residual viable tumor identified on standard H&E evaluation of the radical prostatectomy specimen.

At radical prostatectomy, approximately Day 70
Pathologic downstaging
Ramy czasowe: At radical prostatectomy, approximately Day 70

Proportion of evaluable participants with a lower pathologic T stage at radical prostatectomy compared with baseline clinical T stage.

At radical prostatectomy, approximately Day 70
Proportion of participants with pathologic minimal residual disease (pMRD)
Ramy czasowe: At radical prostatectomy, approximately Day 70

Proportion of evaluable participants with residual viable carcinoma ≤5 mm in the greatest dimension of the largest residual tumor lesion and prostate-confined, lymph-node-negative disease (≤ypT2, ypN0).

At radical prostatectomy, approximately Day 70
Pathologic minimal residual disease (pMRD)
Ramy czasowe: At radical prostatectomy, approximately Day 70

pMRD is defined as residual viable carcinoma ≤5 mm in the greatest dimension of the largest residual tumor lesion with ≤ypT2 and ypN0 disease.

At radical prostatectomy, approximately Day 70
Residual cancer burden (RCB)
Ramy czasowe: At radical prostatectomy, approximately Day 70

RCB will also be quantified, with favorable RCB defined as ≤0.25 cm³ with ≤ypT2 and ypN0 disease.

At radical prostatectomy, approximately Day 70

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Sponsor

Współpracownicy

Śledczy

  • Główny śledczy: Steven Blinka, MD, PhD, Fred Hutchinson Cancer Center

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Szacowany)

30 listopada 2026

Zakończenie podstawowe (Szacowany)

30 listopada 2028

Ukończenie studiów (Szacowany)

30 listopada 2028

Daty rejestracji na studia

Pierwszy przesłany

1 października 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

1 października 2026

Pierwszy wysłany (Rzeczywisty)

6 października 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

6 października 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

1 października 2026

Ostatnia weryfikacja

1 października 2026

Więcej informacji

Terminy związane z tym badaniem

Inne numery identyfikacyjne badania

  • RG1126867

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

NIE

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Tak

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .