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Multitargeted Recombinant Ad5 PSA/MUC-1/Brachyury-Based Immunotherapy (TriAdeno) Vaccine With IL-15 Superagonist N-803 in Participants With Clinically Localized Prostate Cancer Undergoing Active Surveillance

2026年9月17日 更新者:National Cancer Institute (NCI)

Phase II Trial of a Multitargeted Recombinant Ad5 PSA/MUC-1/Brachyury-based Immunotherapy (TriAdeno) Vaccine With IL-15 Superagonist N-803 in Participants With Clinically Localized Prostate Cancer Undergoing Active Surveillance

Background:

Prostate cancer is the second most common cause of cancer-related death among men in the United States. Early-stage, low-grade prostate cancer is managed with active monitoring. However, 35% of men with this cancer will need treatment within 5 years because of tumor growth. Researchers want to know if a new vaccine that targets 3 anti-cancer proteins (TriAdeno) plus a drug (N-803) approved for bladder cancer can help stop prostate tumors from growing.

Objective:

To test TriAdeno and N-803 in people with early-stage prostate cancer.

Eligibility:

People aged 18 years and older with early-stage low- or medium-risk prostate cancer.

Design:

Participants will be screened. They will have a physical exam with blood tests. They will have a test of their heart function. They will have an imaging scan. They may have a rectal exam.

TriAdeno is injected under the skin of the upper thigh; N-803 is injected under the skin of the abdomen. Participants will be treated in up to four 21-day cycles. They will get both injections on the first day of each cycle.

Participants may opt to complete a memory aid: They may record all of their symptoms for 7 days after each injection. They may also complete a questionnaire about their prostate symptoms.

Blood tests, imaging scans, and other tests will be repeated during the study.

A tissue sample (biopsy) of the tumor will be collected during or after cycle 2; a second biopsy may be taken about 1 year later.

Participants will have follow-up phone calls for 5 years....

研究概览

详细说明

Background:

  • Prostate cancer (PCa) is the most common non-cutaneous cancer and second most common cause of cancer-related death among men living in the United States.
  • With increasing detection of localized, low-grade PCa in the prostate-specific antigen (PSA) screening era, active surveillance of PCa has emerged as a viable management strategy in selected, favorable risk population. Though active surveillance is the preferred management strategy for low-grade PCa and an option for selected favorable, intermediate risk disease according to the National Comprehensive Cancer Network (NCCN), up to 35 percent of men will need radical therapy within 5 years due to progression of PCa.
  • Vaccine strategies represent a novel therapeutic approach in the prevention and possible treatment of early-stage PCa. A new trivalent vaccine which targets 3 tumor associated antigens (PSA, brachyury, and MUC-1) has been shown to induce an immune response in a Phase I study of patients with metastatic castrate-resistant PCa.
  • N-803 is an IL-15 agonist that activates and expands T cells and NK cells. N-803 enhances anti-tumor activity in combination with tumor-targeted vaccines. Clinically, multiple studies have demonstrated the safety of tumor-targeted vaccine in combination with PD-1/PD-L1 blockade. Adding N-803 to PD-1/PD-L1 blockade can produce antitumor responses in disease states where responses to PD-1/PD-L1 alone would not be expected.
  • The TriAdeno vaccine has not been evaluated in populations with early stage, low grade PCa.

Primary Objective:

-To determine the effect of an Ad5 PSA/MUC-1/brachyury-based immunotherapy vaccine (TriAdeno) with IL-15 superagonist N-803 on immune infiltration of the local tumor environment by comparing pre- and post-treatment CD8+ and CD4+ T-cell density within the malignant portion of prostate biopsies in participants on active surveillance for low and intermediate risk prostate cancer

Eligibility:

  • Biopsy-proven, organ confined low or intermediate risk adenocarcinoma of the prostate
  • Age >=18 years
  • Serum PSA <20 ng/mL (or <10 ng/mL for participants being treated with 5-alpha reductase inhibitors)
  • Eastern Cooperative Oncology Group (ECOG) performance status <=1

Design:

  • This is an open-label, non-randomized Phase II trial of TriAdeno vaccine given concurrently with N-803 in participants with localized, early stage, low and intermediate risk PCa on active surveillance.
  • The TriAdeno vaccines will be administered subcutaneously (SC) at doses of 5x1011 viral particles (VP) on Day 1 of every 21-day cycle for up to four (4) cycles.
  • N-803 will be administered SC at 15 mcg/kg on Day 1 of every 21-day cycle for up to four (4) cycles.
  • Up to 49 participants may be treated.

研究类型

介入性

注册 (估计的)

52

阶段

  • 阶段2

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

  • 姓名:Peter A Pinto, M.D.
  • 电话号码:(240) 858-3700
  • 邮箱:pp173u@nih.gov

研究联系人备份

学习地点

    • Maryland
      • Bethesda、Maryland、美国、20892
        • National Institutes of Health Clinical Center
        • 接触:

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

  • INCLUSION CRITERIA:
  • Histologically confirmed diagnosis of organ confined, low- or intermediate-risk PCa (Gleason grade group 1 or 2) identified in at least one prostate biopsy core. Biopsies performed at outside institutions should have Gleason score confirmed at the NCI by a genitourinary (GU) pathologist.
  • Participants must be on active surveillance.
  • Pre-study treatment tissue availability (at least one formalin-fixed paraffin embedded [FFPE] biopsy core or one H and E-stained slide and at least 5 unstained slides) obtained between 3 and 24 months prior to treatment initiation is mandatory for study initiation.
  • Serum PSA level of <20 ng/mL (or <10ng/mL for participants being treated with 5- alpha-reductase inhibitors)
  • Clinical stage <=T2a by digital rectal exam (DRE)
  • Age >=18 years
  • Eastern Cooperative Oncology Group (ECOG) performance status <=1.
  • Adequate organ and marrow function as defined below:

    • Absolute neutrophil count (ANC) >=1.0 x 109/L
    • Hemoglobin (Hgb) >=9 g/dL
    • Platelets >=75,000/mcL
    • Prothrombin International Normalized Ratio (INR) <1.5 x upper limit of normal (ULN)
    • Partial thromboplastin time (PTT) <1.5 x ULN
    • Total bilirubin <1.5 x ULN
    • Aspartate aminotransferase (AST) <=2.5 x ULN
    • Alanine aminotransferase (ALT) <=2.5 x ULN
    • Creatinine <=1.5 x ULN

OR

--Calculated Creatinine clearance >=40 mL/min/1.73 m2 for individuals with creatinine levels above institutional normal (using either Chronic Kidney Disease Epidemiology Collaboration [CKD-EPI] equation)

  • Treatment with steroid therapy must have a washout of at least 6 weeks prior to initiation of study treatment. Physiologic (replacement) doses of steroids as well as nasal, topical, or inhaled steroids are allowed.
  • Vaccination with a live (attenuated) vaccine (e.g., FluMist(R)) or a killed (inactivated)/subunit vaccine (e.g., PNEUMOVAX(R), Fluzone(R)) must occur not sooner than 28 days or 14 days, respectively, prior to initiation of study treatment.
  • Participants must agree to use an effective method of contraception (barrier, surgical sterilization, abstinence) for the duration of the study treatment and up to one (1) month after the last vaccine injection. We also will recommend participants with female partners of childbearing potential to ask them to be on highly effective birth control (hormonal, intrauterine device [IUD], surgical sterilization). Participants must not freeze or donate sperm within the same period.
  • Participants must be able to understand and willing to sign a written informed consent document.

EXCLUSION CRITERIA:

  • Prior treatment for PCa by surgery, radiation, local ablative (i.e., cryosurgery or highintensity focused ultrasound), or androgen-deprivation therapy.
  • Evidence of PCa with metastatic disease.
  • Prior treatment with adenovirus-based vector immunotherapy, adenovirus-based vaccines, or investigational vaccines.
  • Prior solid organ or bone marrow transplant.
  • Immunodeficiency or splenectomy.
  • Presence of a known active acute or chronic infection, including human immunodeficiency virus (HIV), confirmed by PCR, and hepatitis B virus (HBV) and hepatitis C virus (HCV), as determined by hepatitis B surface antigen (HBsAg) and HCV serology.
  • History of autoimmune disease (active or past), except for autoimmune-related thyroid disease, type I diabetes, and vitiligo if the condition(s) is well controlled.
  • History of heart disease, such as congestive heart failure (class II, III, or IV defined by the New York Heart Association functional classification), history of unstable or poorly

controlled angina, or history (<1 year prior to initiation of study therapy) of ventricular arrhythmia.

  • Acute or chronic skin disorders that will interfere with injection into the skin of the extremities or subsequent assessment of potential skin reactions.
  • Second malignancy within 3 years prior to initiation of study therapy. Note: Individuals with curatively treated non-melanoma skin cancers or non-muscle invasive bladder cancer will not be excluded.
  • History of herbal products that may decrease PSA levels (e.g., saw palmetto).
  • Participants who have undergone surgery within 4 weeks prior to initiation of study therapy.
  • Participants receiving any other investigational agents within 30 days prior to initiation of study therapy.
  • History of allergic reaction attributed to compounds of similar chemical or biological composition to the study drugs.
  • Uncontrolled intercurrent illness that would limit compliance with study requirements suggested by medical history, physical examination, or standard clinical assessments such as imaging, EKG, and laboratory studies.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Arm 1
TriAdeno vaccine with N-803
The TriAdeno vaccine will be administered on Day 1 of every 21-day cycle for up to 4 cycles.
N-803 will be administered on Day 1 of every 21-day cycle for up to 4 cycles.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
To determine the effect of TriAdeno vaccine with N-803 on immune infiltration of the local tumor environment
大体时间:Baseline/prior to treatment, C2D14 (or as late as C4D21), and optionally at 1 year
Change in the density of T-cell immune infiltrates in the malignant portions of prostate using a paired two sample t-test
Baseline/prior to treatment, C2D14 (or as late as C4D21), and optionally at 1 year

次要结果测量

结果测量
措施说明
大体时间
To assess the adverse events associated with TriAdeno vaccine and N-803
大体时间:Day 1 of each cycle, and through at least 30 days after last treatment
Toxicities will be reported in a descriptive fashion per type, frequency, and grade
Day 1 of each cycle, and through at least 30 days after last treatment
To determine the effect of the TriAdeno vaccines with N-803 on the change in PSA
大体时间:Day 1 of each cycle after C1, 30 days after last treatment, and in follow-up about every 3 months for 1 year and every 6 months for the subsequent 4 years after the end of study therapy
Change in PSA will be analyzed using a paired two sample t-test.
Day 1 of each cycle after C1, 30 days after last treatment, and in follow-up about every 3 months for 1 year and every 6 months for the subsequent 4 years after the end of study therapy

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Peter A Pinto, M.D.、National Cancer Institute (NCI)

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年9月23日

初级完成 (估计的)

2027年6月15日

研究完成 (估计的)

2028年6月15日

研究注册日期

首次提交

2026年5月7日

首先提交符合 QC 标准的

2026年5月7日

首次发布 (实际的)

2026年5月8日

研究记录更新

最后更新发布 (实际的)

2026年9月18日

上次提交的符合 QC 标准的更新

2026年9月17日

最后验证

2026年8月17日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

是的

IPD 计划说明

This study will comply with the NIH Data Management and Sharing (DMS) Policy, which applies to all new and ongoing NIH-funded research in the IRP, as of January 25, 2023, that is associated with a ZIA, with a clinical protocol that undergoes scientific review and/or will involve genomic data sharing.

IPD 共享时间框架

Data will be made available as soon as possible or at the time of associated publication. Data not published in a manuscript will be shared via public source once the data set completes QC.

IPD 共享访问标准

Clinical data will be made available upon request and with the permission of the study Pl. Genomic data are made available via dbGAP through requests to the data custodians.

IPD 共享支持信息类型

  • 研究方案
  • 树液
  • 国际碳纤维联合会

药物和器械信息、研究文件

研究美国 FDA 监管的药品

是的

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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