This Study Evaluates the Diagnostic Performance and Safety of 68Ga-NYM032 PET/CT Imaging in Patients With Suspected Recurrence of Prostate Cancer.

Starting soon · Phase 3

Conditions studied: Prostate Cancer

In brief

This study evaluates the diagnostic performance and safety of 68Ga-NYM032 PET/CT imaging in patients with suspected recurrence of prostate cancer.

Key facts

Study ID

NCT07649122

Run by

Norroy Bioscience Co., LTD

People needed

232

Starts

2026-06-30

Expected to finish

2028-07-31

Last updated by the study team

2026-06-16

Who can join

Age: 18 and older. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

• Patient is male and aged >18 years old.
• Participants with histopathologically confirmed prostate adenocarcinoma, who present with elevated PSA and suspected recurrence following radical prostatectomy and/or radiotherapy and/or other radical prostate cancer treatments (e.g., proton therapy, cryoablation, high-intensity focused ultrasound, etc.). (PSA must be measured within 30 days prior to screening.). (Meeting any one of the following criteria):
• Post-radical prostatectomy (RP): PSA ≥0.2 ng/mL on two consecutive measurements obtained ≥6 weeks after surgery;
• Post-radiotherapy (as defined by the ASTRO-Phoenix consensus): PSA rise ≥2 ng/mL above the PSA nadir;
• Participants with recurrence after other treatments: PSA rise ≥2 ng/mL above the PSA nadir.
• ECOG performance status 0-2; expected survival ≥ 6 months.
• Ability to understand a written informed consent document, and the willingness to sign it.

You may not qualify if…

• Participants who have previously participated in other interventional clinical trials and are within five physical half-lives, or have received radionuclide agents previously with an interval of less than ten physical half-lives prior to study drug injection.
• Participants administered any IV iodinated contrast medium within 24 hours, or any high density oral contrast medium (oral water contrast is acceptable) within 5 days, prior to study drug injection.
• Known hypersensitivity to the active ingredient or excipients of the study drug.
• Participants not capable of getting PET study , or inability to lay still for the duration of the exam.
• Any medical condition or circumstance that, in the investigator's judgment, may compromise study safety or patient compliance.

Full record on ClinicalTrials.gov

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