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An External Control Arm Study Comparing Survival Among Metastatic Castration-Resistant Prostate Cancer (mCRPC) Patients Treated With 177Lu-PSMA-617 vs Androgen Receptor Pathway Inhibitor (ARPI) Switch in Routine Care

2026年9月28日 更新者:Novartis Pharmaceuticals

Comparing the Lutetium (177Lu) Vipivotide Tetraxetan Arm of the PSMAfore Clinical Trial to a Switch in Androgen Receptor Pathway Inhibitor (ARPI) as External Control Arm (ECA) Using a Real-world Data Source for Patients With Metastatic Castration-Resistant Prostate Cancer (mCRPC) After Progression on Prior ARPI

The aim of this study is to assess the effectiveness of 177Lu-PSMA-617 (lutetium (177Lu) vipivotide tetraxetan) on survival in patients randomized to receive treatment following progression on one ARPI from the PSMAfore trial compared to the effectiveness of a change in ARPI treatment on survival in a real-world setting in patients with mCRPC who are taxane-naive but have progressed after a switch in ARPI.

研究概览

地位

完全的

研究类型

观察性的

注册 (实际的)

1525

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。

学习地点

      • Basel、瑞士、CH-4056
        • Novartis

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

18年 至 100年 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

男性

取样方法

非概率样本

研究人群

PSMAfore trial patients with mCRPC who progressed once after treatment with an ARPI and were taxane-naive, and real-world data (RWD) mCRPC patients from the United States (US)-based health research database who were taxane-naive and had evidence of treatment with a change in ARPI immediately following progression.

描述

Inclusion criteria:

  1. Had an International Classification of Diseases, 9th or 10th Revision, Clinical Modification (ICD-9-CM or ICD-10-CM) diagnosis of prostate cancer (PC) (ICD-9-CM 185x or ICD-10-CM C61x).
  2. Had at least two documented clinical visits, on different days, occurring on or after 01 Jan 2013.
  3. Included in probabilistic sample of patients queued for review via abstraction.
  4. Had diagnosis of metastatic disease on or after 01 Jan 2013.
  5. Histology was confirmed as adenocarcinoma of the prostate.
  6. Had confirmed mCRPC diagnosis.
  7. Treated with an ARPI-containing line of therapy (LOT; i.e., index therapy) in the mCRPC setting immediately after progression on one previous ARPI-containing line (in any setting, Hormone Sensitive PC or castration-resistant PC), as defined per the health research database's LOT rules and confirmed via abstraction.
  8. 18 years of age or older at the start of index therapy.
  9. Had an Eastern Cooperative Oncology Group Performance Score (ECOG PS) of 0-1 within 30 days before or up to 7 days after index date, or unknown ECOG PS.

Exclusion criteria:

  1. Female sex.
  2. Had evidence of untreated brain metastases.
  3. Had history of cardiac comorbidities, infection with hepatitis B or C, or spinal cord compression that would indicate significant risk to PSMAfore trial participation.
  4. Diagnosis of an active additional malignancy (i.e., other than prostate cancer).
  5. Evidence of biomarker status that would indicate eligibility for treatment other than ARPI, or better prognosis.
  6. Evidence of prior treatment with therapies that potentially affect study outcomes (e.g., radiopharmaceuticals, taxane, immunotherapy or biological therapy, clinical study drug (CSD), or 177Lu-PSMA-617).
  7. Had evidence of inadequate organ function.
  8. Had evidence of low levels of albumin (< 2.5 g/dL).
  9. Had evidence of a negative PSMA-PET scan.

Other protocol-defined inclusion/exclusion criteria may apply.

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

  • 观测模型:COHORT
  • 时间观点:RETROSPECTIVE

队列和干预

团体/队列
External Control Arm (ECA)

RWD patients with mCRPC who were treated with a change in ARPI after progression on prior ARPI and before taxane treatment.

PSMAfore Trial Treatment Arm (TTA)

PSMAfore trial patients with mCRPC who were treated with 177Lu-PSMA-617 after progression on one ARPI.

PSMAfore Trial Control Arm (TCA)

PSMAfore trial patients with mCRPC who switched to a subsequent ARPI after progression on a prior ARPI.

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
Overall Survival (OS) of the TTA Group
大体时间:Up to approximately 3 years and 6 months

OS defined as time from randomization to death due to any cause.

Up to approximately 3 years and 6 months
Real-world Overall Survival (rwOS) of the ECA Group (for the Primary Measure)
大体时间:Up to approximately 7 years

rwOS is defined as the time from initiation of the index ARPI to death due to any cause.

Up to approximately 7 years

次要结果测量

结果测量
大体时间
OS of the TCA Group
大体时间:Up to approximately 3 years and 6 months
Up to approximately 3 years and 6 months
rwOS of the ECA Group (for the Secondary Measure)
大体时间:Up to approximately 7 years
Up to approximately 7 years

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

  • 研究主任:Novartis Pharmaceuticals、Novartis Pharmaceuticals

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 (实际的)

2024年3月1日

初级完成 (实际的)

2025年10月1日

研究完成 (实际的)

2025年10月1日

研究注册日期

首次提交

2026年9月21日

首先提交符合 QC 标准的

2026年9月21日

首次发布 (实际的)

2026年9月28日

研究记录更新

最后更新发布 (实际的)

2026年10月1日

上次提交的符合 QC 标准的更新

2026年9月28日

最后验证

2026年9月1日

更多信息

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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