Adenocarcinoma of the Prostate

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Review clinical trials related to Adenocarcinoma of the Prostate. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Study of PSMA-targeted Therapy and Androgen Receptor Suppression in Low-volume Metastatic ProstatE Cancer: SPARKLE Trial

This phase II trial tests leuprolide acetate alone versus in combination with 177Lu-PSMA-617, with or without abiraterone acetate and prednisone, for the treatment of hormone-sensitive prostate cancer has spread to a limited number of anatomic sites at the time of initial diagnosis (de novo low volume metastasis) or that has come back after a period of improvement (recurrent). Standard of care treatment for prostate cancer usually includes androgen deprivation therapy, with or without abiraterone acetate and prednisone. Leuprolide acetate is a form of androgen deprivation therapy. It blocks the body from making testosterone (a male hormone) and estradiol (a female hormone). It may stop the growth of prostate cancer cells that need testosterone to grow. 177Lu-PSMA-617 is a type of radioconjugate drug. Upon administration, vipivotide tetraxetan targets and binds to prostate specific membrane antigen (PSMA)-expressing tumor cells. Upon binding, PSMA-expressing tumor cells are destroyed by 177Lu through the specific delivery of radiation. PSMA, a tumor-associated antigen and type II transmembrane protein, is overexpressed on prostate tumor cells. Abiraterone acetate is a type of anti-androgen drug. It blocks tissues from making androgens (male hormones), such as testosterone. This may cause the death of cancer cells that need androgens to grow. Prednisone is in a class of medications called corticosteroids. It is used to reduce inflammation and lower the body's immune response to help lessen the side effects of chemotherapy drugs. Giving 177Lu-PSMA-617 in combination with leuprolide acetate, with or without abiraterone acetate and prednisone, may be more effective at treating patients with recurrent or de novo low volume metastatic hormone-sensitive prostate cancer than giving leuprolide acetate alone.

Participants needed: 202
Trial details
Phase: Phase 2Age: 18+Biological sex: MaleType: InterventionalSponsor: Mayo ClinicUpdated: Jun 17, 2026Locations: 1
Eligibility criteria

Male patients aged 18 years or older [+20]

PSMA-undetectable disease defined as rising prostate specific antigen (PSA) with... [+12]

Status: Recruiting

Prospective Prostate Cancer and Patient-reported Outcomes Registry

This study aims to evaluate the use of a digital solution, integrated into the electronic health record, for prospective and structured reporting of clinical and patient-reported outcomes for patients diagnosed with localized or locally advanced prostate cancer.

Participants needed: 5,000
Trial details
Age: 18+Biological sex: MaleType: ObservationalSponsor: Universitaire Ziekenhuizen KU LeuvenUpdated: May 22, 2024Locations: 4Duration: 10 Years
Eligibility criteria

Pathology confirmed diagnosis of localized or locally advanced prostate cancer [+2]

Patients with prior treatment for prostate malignancies will be excluded. [+3]