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临床试验/2024-512754-16-00
2024-512754-16-00撤回3 期

A Phase 3, Multicenter, Open-label Study to Test the Diagnostic Performance of Copper Cu 64 PSMA I&T PET/CT in Staging of Men with Newly Diagnosed Unfavorable Intermediate-risk, High-risk or Very High-risk Prostate Cancer Electing to Undergo Radical Prostatectomy with Pelvic Lymph Node Dissection

Curium US LLC29 个研究点 分布在 3 个国家目标入组 150 人开始时间: 2024年9月16日最近更新:
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相关药物

试验速览

阶段
3 期
状态
撤回
发起方
Curium US LLC
入组人数
150
试验地点
29
主要终点
1. The sensitivity of copper Cu 64 PSMA I&T PET/CT to determine the presence of metastatic pelvic lymph nodes relative to histopathology reference standard. At least one positive pelvic lymph node on the PET scan and one positive lymph node as determined by histopathology on the same side of the pelvis (left or right) will be counted a true positive at the patient level.

研究概览

简要总结

Primary Objective and Endpoints To determine the diagnostic performance of copper Cu 64 PSMA I&T PET/CT for the detection of presence or absence of pelvic lymph node metastasis in pre-prostatectomy patients with unfavorable intermediate-risk, high-risk or very high-risk PC.

入排标准

年龄范围
18 years 至 65+ years(18-64 Years, 65+ Years)
性别
Male
接受健康志愿者

入选标准

  • Patients with histologically proven prostate adenocarcinoma.
  • Planned prostatectomy with pelvic lymph node dissection.
  • Unfavorable intermediate-risk, high-risk, or very high-risk disease defined by NCCN Guidelines Version 1.2023 and previous versions.
  • Male aged ≥18 years.
  • Able to understand and provide signed written informed consent.

排除标准

  • Androgen deprivation therapy, neoadjuvant chemotherapy, radiation therapy (including local ablation techniques), or any investigational therapy against PC prior to prostatectomy.
  • Patients participating in an interventional clinical trial within 30 days and having received an IP within five (5) biological half-lives prior to administration.
  • Patients with any medical condition or circumstance (including receiving an IP or capable of having a PET study) that the investigator believes may compromise the data collected or lead to a failure to fulfil the study requirements.
  • Patients who are planned to have an x-ray contrast within 24 hours or other PET radiotracer < within 10 physical half-lives prior to the PET scan. If Barium contrast is administered this should be cleared before the PET scan.
  • Patients who are administered any high energy (>300 KeV) gamma emitting radioisotopes within five (5) physical half-lives prior to copper Cu 64 PSMA I&T administration.
  • Patients with known hypersensitivity to the active substance or any of the excipients of the IP.
  • Patients who had a PSMA PET as part of their standard medical care within 90 days prior to enrollment

结局指标

主要结局

1. The sensitivity of copper Cu 64 PSMA I&T PET/CT to determine the presence of metastatic pelvic lymph nodes relative to histopathology reference standard. At least one positive pelvic lymph node on the PET scan and one positive lymph node as determined by histopathology on the same side of the pelvis (left or right) will be counted a true positive at the patient level.

1. The sensitivity of copper Cu 64 PSMA I&T PET/CT to determine the presence of metastatic pelvic lymph nodes relative to histopathology reference standard. At least one positive pelvic lymph node on the PET scan and one positive lymph node as determined by histopathology on the same side of the pelvis (left or right) will be counted a true positive at the patient level.

2. The specificity of copper Cu 64 PSMA I&T PET/CT to determine the absence of metastatic pelvic lymph nodes relative to histopathology reference standard. Negative pelvic lymph node on the PET scan and negative pelvic lymph nodes as determined by histopathology on the same side of the pelvis (Left or Right) will be counted a true negative at the patient level.

2. The specificity of copper Cu 64 PSMA I&T PET/CT to determine the absence of metastatic pelvic lymph nodes relative to histopathology reference standard. Negative pelvic lymph node on the PET scan and negative pelvic lymph nodes as determined by histopathology on the same side of the pelvis (Left or Right) will be counted a true negative at the patient level.

次要结局

  • 1. Reader kappa statistics of copper Cu 64 PSMA I&T PET/CT scan interpretation by the blinded independent readers.
  • 2. Treatment-emergent adverse events from the time of IP administration up to 72 hours.

研究者

发起方
Curium US LLC
申办方类型
Pharmaceutical company
责任方
Principal Investigator
主要研究者

Anni Morsing, Curium Denmark

Scientific

Curium US LLC

研究点 (29)

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