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RECRUITING Phase 1

64Cu-SAR-bisPSMA and 67Cu-SAR-bisPSMA for Identification and Treatment of PSMA-expressing Metastatic Castrate Resistant Prostate Cancer (SECuRE)

NCT04868604 · View on ClinicalTrials.gov ↗

Study Summary

The aim of this study is to determine the safety and efficacy of 67Cu-SAR-bisPSMA in participants with PSMA-expressing metastatic castrate resistant prostate cancer.

Interventions

  • DRUG 64Cu-SAR-bisPSMA
  • DRUG 67Cu-SAR-bisPSMA

Study Locations (7)

California

  • Stanford Cancer Institute — Stanford

Louisiana

  • East Jefferson General Hospital — River Ridge

Michigan

  • BAMF Health — Grand Rapids

Minnesota

  • Mayo Clinic — Rochester

Missouri

  • Washington University School of Medicine at Barnes-Jewish Hospital — St Louis

Nebraska

  • XCancer — Omaha

New York

  • Weill Cornell Medicine at New York-Presbyterian — New York

Trial Details

FieldValue
Enrollment Target 54 participants
Start Date 2021-08-11
Est. Completion 2026-09
Phase Phase 1

Sponsor

Clarity Pharmaceuticals

3 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04868604

The ClinicalTrials.gov registry entry for NCT04868604 describes a study currently listed as recruiting. It is categorized as Phase 1, 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 54 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 1 condition, with Prostatic Neoplasms, Castration-Resistant appearing as the primary indexed condition, and to 2 interventions — 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: NCT04868604 reports 7 study locations spanning 7 distinct geographic areas — top geographies include California, Louisiana, Michigan. 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 NCT04868604 about?

NCT04868604 is a clinical study titled "64Cu-SAR-bisPSMA and 67Cu-SAR-bisPSMA for Identification and Treatment of PSMA-expressing Metastatic Castrate Resistant Prostate Cancer (SECuRE)". The aim of this study is to determine the safety and efficacy of 67Cu-SAR-bisPSMA in participants with PSMA-expressing metastatic castrate resistant prostate cancer.

What is the current status of trial NCT04868604?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 54 participants. The study started on 2021-08-11. Estimated completion is 2026-09.

What conditions does trial NCT04868604 study?

This clinical trial studies the following conditions: Prostatic Neoplasms, Castration-Resistant. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04868604?

The interventions under investigation include: 64Cu-SAR-bisPSMA (DRUG), 67Cu-SAR-bisPSMA (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04868604?

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 NCT04868604 being conducted?

This trial has 7 study locations across California, Louisiana, Michigan, Minnesota, Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial