64Cu-SAR-bisPSMA PET for High-risk Prostate Cancer

Positron Emission Tomography Using 64Cu-SAR-bisPSMA in Participants With High-risk Prostate Cancer Prior to Radical Prostatectomy

Recruiting Phase 3 Interventional Study
Prostate Cancer Prostatic Neoplasms
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Pivotal Trial This treatment is in the last trial phase before FDA approval. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Male
Trial phase
Phase 3
Study type
Interventional
Purpose
Diagnostic
Participants needed
383 (estimated)
Sponsor
Clarity Pharmaceuticals Ltd · Industry
Who this trial is looking for

This trial is looking for men with untreated, high-risk prostate cancer. Participants will undergo a special scan called a PET scan to help find cancer spread before surgery.

Are You a Good Fit for This Trial?

You may be able to join if

  • I am at least 18 years old.
  • I have signed an informed consent form.
  • I have untreated prostate cancer that has been confirmed by a test.
  • I meet high-risk criteria for prostate cancer.
  • I plan to have surgery for my prostate cancer.

You may not be able to join if

  • I have received a high-energy radioisotope in the last several weeks.
  • I am allergic to 64Cu-SAR-bisPSMA or any of its parts.
  • I have a type of prostate cancer that is mostly small cell or neuroendocrine.

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.

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About This Trial

The aim for this study is to assess the diagnostic performance of 64Cu-SAR-bisPSMA PET to detect regional nodal metastases.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * At least 18 years of age. * Signed informed consent. * Untreated, histologically confirmed adenocarcinoma of the prostate. * High-risk or greater PC defined by National Comprehensive Cancer Network Guidelines Version 1.202327 (clinical stage ≥T3a, or Grade Group ≥4, or PSA \>2…
Contacts

Clarity Pharmaceuticals

+61 (0) 2 9209 4037

clinicaltrials@claritypharmaceuticals.com

CONTACT