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Testing Pasritamig Before Surgery for the Treatment of Localized Prostate Cancer

1 octobre 2026 mis à jour par: 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.

Aperçu de l'étude

Statut

Pas encore de recrutement

Les conditions

Intervention / Traitement

Type d'étude

Interventionnel

Inscription (Estimé)

18

Phase

  • La phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Lieux d'étude

    • Washington
      • Seattle, Washington, États-Unis, 98109
        • Fred Hutch/University of Washington Cancer Consortium
        • Contact:
        • Chercheur principal:
          • Steven Blinka, MD, PhD

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans et plus (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Homme

La description

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 d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: N / A
  • Modèle interventionnel: Affectation à un seul groupe
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: 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

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Feasibility of neoadjuvant pasritamig
Délai: 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
Délai: 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

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Adverse pathologic features
Délai: 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)
Délai: Screening through approximately 12 weeks following radical prostatectomy
Screening through approximately 12 weeks following radical prostatectomy
Time to biochemical recurrence or death
Délai: 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)
Délai: 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
Délai: 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)
Délai: 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)
Délai: 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)
Délai: 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

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Collaborateurs

Les enquêteurs

  • Chercheur principal: Steven Blinka, MD, PhD, Fred Hutchinson Cancer Center

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

30 novembre 2026

Achèvement primaire (Estimé)

30 novembre 2028

Achèvement de l'étude (Estimé)

30 novembre 2028

Dates d'inscription aux études

Première soumission

1 octobre 2026

Première soumission répondant aux critères de contrôle qualité

1 octobre 2026

Première publication (Réel)

6 octobre 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

6 octobre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

1 octobre 2026

Dernière vérification

1 octobre 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Oui

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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