Clinical trials

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Condition / disease
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Status: Not yet recruiting

A Phase 2 Trial of 61Cu-NU101 PET/CT Compared Against Current Standard-of-care 18F-piflufolastat (Pylarify®) PET/CT.

The purpose of this research is to test whether a new investigational Molecular Imaging (MI) agent called 61Cu-NU101 is equal to or better than a currently used MI agent, Pylarify, for the detection of prostate cancer metastases. 34 participants with biopsy-proven prostate cancer and cancer seen on a Pylarify PET scan will be enrolled in this study. The investigational 61Cu-NU101 PET/CT will be perfromed. If there is a difference between the standard Pylarify exam and the investigational 61Cu-NU101 exam, a biopsy of one lesion that is different between the two exams may be performed.

Participants needed: 34
Trial details
Phase: Phase 2Age: 18+Biological sex: MaleType: InterventionalSponsor: Hoag Memorial Hospital PresbyterianUpdated: Jun 9, 2026Locations: 2
Eligibility criteria

Biopsy proven prostate adenocarcinoma [+2]

Known allergy/hypersensitivity to PSMA-targeted imaging agents [+1]

Status: Recruiting

A Phase I Trial of 61Cu-NODAGA-PSMA for Patients with Prostate Cancer

Molecular Imaging (MI) uses tracers which emit radiation to provide clinically valuable imaging for patient with cancer. Most current MI agents utilize Fluorine 18 or Gallium 68 as the positron emitter for PET imaging. However, these isotopes have short half-lives which limit the geographic distribution range of tracers made with these isotopes. Copper 61 (61Cu) has a 3.3 hour half-life, which would allow for far greater distribution range following radiotracer production. This phase I trial will test the safety and effectiveness of a novel MI radiotracer that uses 61Cu as its positron emitting isotope and targets Prostate Specific Membrane Antigen (PSMA) for imaging prostate cancer. A successful trial will provide the ability to advance this novel 61Cu-NODAGA-PSMA radioisotope into phase II trials, as well as open a new paradigm into the production of MI radioisotopes with 61Cu.

Participants needed: 8
Trial details
Phase: Phase 1Age: 18+Biological sex: MaleType: InterventionalSponsor: Hoag Memorial Hospital PresbyterianUpdated: Dec 16, 2024Locations: 1
Eligibility criteria

Biopsy proven prostate adenocarcinoma [+4]

Known allergy/hypersensitivity to PSMA-targeted imaging agents [+1]

Status: Recruiting

Perioperative Mindfulness Proposal

The purpose of this study is to determine if a regular meditation and breath work practice started before surgery and continued through post-surgical recovery can improve anxiety and pain related to breast cancer and its treatment.

Participants needed: 24
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Hoag Memorial Hospital PresbyterianUpdated: Oct 15, 2024Locations: 1
Eligibility criteria

Females 18 years of age or older [+5]

Recurrent breast cancer [+9]

Status: Recruiting

PyL in Patients With High Risk and Biochemically Recurrent Prostate Cancer

The standard of care imaging of prostate cancer metastases recommended by the National Comprehensive Cancer Network (NCCN), CT of the chest/abdomen/pelvis and bone scan, may be suboptimal. PyL is a novel PET tracer designed to detect prostate specific membrane antigen (PSMA) expressed on prostate cancer cells. PyL PET/CT may provide improved evaluation of clinically significant metastases in patients with prostate cancer.

Participants needed: 184
Trial details
Phase: Phase 2Age: 18+Biological sex: MaleType: InterventionalSponsor: Hoag Memorial Hospital PresbyterianUpdated: Jul 27, 2021Locations: 1
Eligibility criteria

Male ≥ 18 years of age. [+1]

Presence of a condition or abnormality that in the opinion of the Investigator w... [+2]