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

Sponsor: Jonsson Comprehensive Cancer Center

Expanded Access
Approved for Marketing
Sponsor score: 40
Inactive

ClinicalTrials ID:NCT04348682

Patient View

This expanded access protocol allows eligible patients with prostate cancer to undergo 68Ga-PSMA-11 PET imaging for accurate detection and staging. Participants include those with biochemical recurrence or preprostatectomy staging. The intervention involves a single intravenous dose of 68Ga-PSMA-11, followed by PET/CT imaging after 50-100 minutes.

Patient Parameters

Program Overview

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.

Description

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.

Eligibility Criteria

Inclusion Criteria

  • 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).

  • Age > 18.

  • Ability to understand a written informed consent document, and the willingness to sign it.

    i.

Exclusion Criteria

  • 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).

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