64Cu-SAR-bisPSMA Positron Emission Tomography: A Phase 3 Study of Participants With Biochemical Recurrence of Prostate Cancer

Clinicaltrials.gov ID: NCT06970847
db-list-check Status RECRUITING
b-loader Phase PHASE3
b-people Age ≥ 18 Years
b-bullseye-arrow Enrollments 220

Conditions

Prostate Cancer, Prostate Cancer Patients With Detectable PSA Following Prostatectomy, Prostate Cancer Recurrent, Prostate Cancer Patients Who Have Brachytherapy Seed Implant, Prostate Cancer Patients Treated by Radiotherapy, Cryotherapy

Drugs

64Cu-SAR-bisPSMA

Summary

The aim for this study is to investigate the ability of 64Cu-SAR-bisPSMA PET/CT to detect recurrence of prostate cancer

Locations

3 locations Found with status Recruiting

Status

  • RECRUITING

Contact Person

  • Frankis Almaguel, MD

Status

  • RECRUITING

Contact Person

  • Luke Nordquist, MD

Status

  • RECRUITING

Contact Person

  • Naveen Kella, MD

Eligibility Criteria

Inclusion Criteria:

1. At least 18 years of age.
2. Signed informed consent.
3. Life expectancy ≥ 6 months as determined by the Investigator.
4. Histologically confirmed adenocarcinoma of prostate per original diagnosis and completed subsequent definitive therapy.
5. Participant potentially eligible for salvage therapy with curative intent.
6. PSA level after definitive therapy:

1. Post-radical prostatectomy: Detectable or rising PSA that is ≥ 0.2 ng/mL with a confirmatory PSA ≥ 0.2 ng/mL (per AUA recommendation) or
2. Post-radiation therapy, cryotherapy, or brachytherapy: Increase in PSA level that is elevated by ≥ 2 ng/mL above the nadir (per ASTRO-Phoenix consensus definition).
7. Participant willing to undergo biopsy of a 64Cu-SAR-bisPSMA PET-positive lesion for histological confirmation of PC, where this is safe and feasible.
8. An Eastern Cooperative Oncology performance status of 0-2.

Exclusion Criteria:

1. Participants who received investigational agent within 5 biological half-lives prior to Day 1.
2. Participants administered any high energy (>300 KeV) gamma-emitting radioisotope within 5 physical half-lives prior to Day 1.
3. Previous systemic therapy for PC (with the exception of neoadjuvant and adjuvant systemic therapy as part of the definitive therapy).
4. Ongoing treatment or treatment within 6 months of Day 1 with any systemic therapy (e.g. any investigational therapy, androgen-deprivation therapy, antiandrogen, gonadotropin-releasing hormone, luteinizing hormone-releasing hormone agonist or antagonist, chemotherapy, immunotherapy or radiotherapy) for PC.
5. Known or expected hypersensitivity to 64Cu-SAR-bisPSMA or any of its components.
6. Any serious medical condition or extenuating circumstance (including receiving the investigational product or not capable of having a PET scan) which the investigator feels may interfere with the procedures or evaluations of the study.

Study Plan

64Cu-SAR-bisPSMA 200MBq 64Cu-SAR-bisPSMA.

  • DRUG:

    64Cu-SAR-bisPSMA

    Description:

    All Patients will receive a single administration, a bolus injection of 200MBq 64Cu-SAR-bisPSMA

Outcome Measures

Primary Outcome Measures

Ability of 64Cu-SAR-bisPSMA PET/CT to detect recurrence of prostate cancer

Time Frame: Up to 52 Weeks

Secondary Outcome Measures

To investigate the safety and tolerability of 64-CuSAR-bisPSMA

Time Frame: Up to 52 Weeks

To assess the participants-level PPV of 64Cu-SAR-bisPSMA PET/CT

Time Frame: Up to 52 Weeks

To assess the participant-level DR of 64Cu-SAR-bisPSMA PET/CT

Time Frame: Up to 52 Weeks

To determine the efficacy of 64Cu-SAR-bisPSMA PET/CT in participants with negative or equivocal conventional imaging at baseline

Time Frame: Up to 52 Weeks

To determine the effect of the composition of Reference Standard on the performance of 64Cu-SAR-bisPSMA PET/CT

Time Frame: Up to 52 Weeks

To evaluate the consistency among readers and the reproducibility of the 64Cu-SAR-bisPSMA PET/CT readings

Time Frame: Up to 52 Weeks

To evaluate the consistency among readers and the reproducibility of the 64Cu-SAR-bisPSMA PET/CT readings

Time Frame: Up to 52 Weeks

To determine the efficacy of 64Cu-SAR-bisPSMA PET/CT in participants with negative or equivocal conventional imaging at baseline

Time Frame: Up to 52 Weeks

To determine the effect of the composition of Reference Standard on the performance of 64Cu-SAR-bisPSMA PET/CT

Time Frame: Up to 52 Weeks

Timeline

  • Last Updated
    July 17, 2025
  • Start Date
    May 14, 2025
  • Today
    November 9, 2025
  • Completion Date ( Estimated )
    December 31, 2026

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