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64Cu-SAR-bisPSMA Positron Emission Tomography: A Phase 3 Study of Participants With Biochemical Recurrence of Prostate Cancer
NCT06970847 · View on ClinicalTrials.gov ↗
Study Summary
The aim for this study is to investigate the ability of 64Cu-SAR-bisPSMA PET/CT to detect recurrence of prostate cancer
Conditions Studied
Interventions
- DRUG 64Cu-SAR-bisPSMA
Study Locations (20)
California
- UC Irvine — Irvine
- Comprehensive Urology Medical Group — Los Angeles
- Alarcon Urology Center — Montebello
Florida
- University of Florida Health- Jacksonville — Jacksonville
- Biogenix Molecular — Miami
Arizona
- East Valley Urology Center of Arizona — Mesa
Arkansas
- Arkansas Urology Research Center — Little Rock
Illinois
- Endeavor Health — Evanston
Indiana
- Indiana University Health-IU Simon Cancer Center — Indianapolis
Kansas
- Wichita Urology Group — Wichita
Louisiana
- XCancer Research Network / LCMC Health EJGH — Metairie
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 220 participants |
| Start Date | 2025-05-16 |
| Est. Completion | 2026-12-31 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06970847
The ClinicalTrials.gov registry entry for NCT06970847 describes a study currently listed as recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 220 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Clarity Pharmaceuticals, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 6 conditions, with Prostate Cancer appearing as the primary indexed condition, and to 1 intervention — of which 64Cu-SAR-bisPSMA is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06970847 reports 20 study locations spanning 17 distinct geographic areas — top geographies include California, Florida, Arizona. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06970847 about?
NCT06970847 is a clinical study titled "64Cu-SAR-bisPSMA Positron Emission Tomography: A Phase 3 Study of Participants With Biochemical Recurrence of Prostate Cancer". The aim for this study is to investigate the ability of 64Cu-SAR-bisPSMA PET/CT to detect recurrence of prostate cancer
What is the current status of trial NCT06970847?
This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 220 participants. The study started on 2025-05-16. Estimated completion is 2026-12-31.
What conditions does trial NCT06970847 study?
This clinical trial studies the following conditions: Prostate Cancer, Prostate Cancer Recurrent, Prostate Cancer Patients Treated by Radiotherapy, Prostate Cancer Patients With Detectable PSA Following Prostatectomy, Prostate Cancer Patients Who Have Brachytherapy Seed Implant. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06970847?
The interventions under investigation include: 64Cu-SAR-bisPSMA (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06970847?
This trial is sponsored by Clarity Pharmaceuticals, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06970847 being conducted?
This trial has 20 study locations across Arizona, Arkansas, California, Florida, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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