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临床试验/NCT04348682
NCT04348682Approved For Marketing不适用

Expanded Access Protocol of 68Ga-PSMA-11 for Prostate Cancer PET Imaging

Jonsson Comprehensive Cancer Center1 个研究点 分布在 1 个国家开始时间: 2020年4月16日最近更新:
适应症

试验速览

阶段
不适用
状态
Approved For Marketing
试验地点
1

研究概览

简要总结

To provide expanded access to 68Ga-PSMA-11 PET imaging for eligible participants to detect and localize prostate cancer for initial and subsequent treatment strategy.

详细描述

Prostate-specific membrane antigen (PSMA) targeted Positron Emission Tomography (PET) imaging has been embraced enthusiastically worldwide. Given the unmet clinical need for accurately diagnosing and staging prostate cancer and the encouraging results of 68Ga-PSMA-11 PET worldwide, University of California Los Angeles (UCLA) and University of California San Francisco (UCSF) conducted pivotal registration trials to assess 68Ga-PSMA-11's safety and efficacy profile in detecting prostate cancer in adult patients. To gap the unmet clinical need of 68Ga-PSMA-11 PET during the period prior to FDA approval, UCLA Nuclear Medicine offers expanded access of this investigational PET drug to eligible participants.

研究设计

研究类型
Expanded Access

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Histopathological proven prostate adenocarcinoma.
  • Rising prostatic specific antigen(PSA) after definitive therapy with prostatectomy or radiation therapy.
  • Post radical prostatectomy (RP)
  • PSA equals to or greater than 0.2 ng/mL measured more than 6weeks after RP
  • Post-radiation therapy -ASTRO-Phoenix consensus definition
  • Nadir + greater than or equal to 2 ng/mL rise in PSA
  • Karnofsky performance status of ≥ 50 (or Eastern Cooperative Oncology Group (ECOG)/ World Health Organization (WHO) equivalent).
  • Ability to understand a written informed consent document, and the willingness to sign it.

排除标准

  • Concomitant investigational therapy.
  • Known inability to lie flat, remain still or tolerate a PET scan.
  • Patient undergoing active treatment for non-prostate malignancy, other than skin basal cell or cutaneous superficial squamous cell carcinoma that has not metastasized and superficial bladder cancer.
  • Preprostatectomy Staging Population:
  • ii. Inclusion criteria:
  • Biopsy proven prostate adenocarcinoma.
  • Considered for prostatectomy with lymph node dissection.
  • Intermediate to high-risk disease (as determined by elevated PSA [PSA>10], T-stage [T2b or greater], Gleason score [Gleason score > 6] or other risk factors).
  • Able to provide written consent.
  • Karnofsky performance status of ≥50 (or ECOG/WHO equivalent).
  • ii. Exclusion criteria:
  • Patients not capable of getting PET study due to weight, claustrophobia, or inability to lay still for the duration of the exam.
  • Neoadjuvant chemotherapy, radiation therapy or any definitive local therapy prior to prostatectomy including focal ablation techniques (HiFu).

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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