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Testing Pasritamig Before Surgery for the Treatment of Localized Prostate Cancer

1 ottobre 2026 aggiornato da: 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.

Panoramica dello studio

Stato

Non ancora reclutamento

Condizioni

Intervento / Trattamento

Tipo di studio

Interventistico

Iscrizione (Stimato)

18

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

Luoghi di studio

    • Washington
      • Seattle, Washington, Stati Uniti, 98109
        • Fred Hutch/University of Washington Cancer Consortium
        • Contatto:
        • Investigatore principale:
          • Steven Blinka, MD, PhD

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

18 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Maschio

Descrizione

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).

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: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 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

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Feasibility of neoadjuvant pasritamig
Lasso di tempo: 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
Lasso di tempo: 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

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Adverse pathologic features
Lasso di tempo: 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)
Lasso di tempo: Screening through approximately 12 weeks following radical prostatectomy
Screening through approximately 12 weeks following radical prostatectomy
Time to biochemical recurrence or death
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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

Collaboratori e investigatori

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

Sponsor

Collaboratori

Investigatori

  • Investigatore principale: Steven Blinka, MD, PhD, Fred Hutchinson Cancer Center

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)

30 novembre 2026

Completamento primario (Stimato)

30 novembre 2028

Completamento dello studio (Stimato)

30 novembre 2028

Date di iscrizione allo studio

Primo inviato

1 ottobre 2026

Primo inviato che soddisfa i criteri di controllo qualità

1 ottobre 2026

Primo Inserito (Effettivo)

6 ottobre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

6 ottobre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

1 ottobre 2026

Ultimo verificato

1 ottobre 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • RG1126867

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

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

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 .