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Metastatic Prostate Cancer clinical trials

View clinical trials related to Metastatic Prostate Cancer.

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NCT ID: NCT06439225 Not yet recruiting - Clinical trials for Metastatic Castration-resistant Prostate Cancer

Platinum and Taxane Chemo in Met Castration Resistant Prostate Cancer Patients With Alterations in DNA Damage Response Genes

OPTION-DDR
Start date: July 31, 2024
Phase: Phase 3
Study type: Interventional

The usual approach for most patients who are not in a study is treatment with docetaxel. This study is being done to answer the following question: Can the chance of prostate cancer growing or spreading be lowered by adding a drug to the usual approach? This study is being done to find out if this approach is better or worse than the usual approach for prostate cancer. The usual approach is defined as the care most people get for prostate cancer.

NCT ID: NCT06429813 Not yet recruiting - Clinical trials for Metastatic Prostate Cancer

Remotely Monitored Exercise Interventions in Patients With mCSPC Undergoing ADT (Prostate 006)

Start date: July 2024
Phase: N/A
Study type: Interventional

This study consists of two home-based exercise programs: a stationary exercise bicycle intervention (Arm A), and a walking intervention (Arm B). The study will enroll 24 patients who are starting ADT (Androgen Deprivation Therapy)/ARSI (Androgen-Receptor Signaling Inhibitors) therapy for newly diagnosed metastatic castrate-sensitive prostate cancer (mCSPC). All participants will be asked to complete 1-2 training sessions at UVA prior to starting the exercise. All participants will be asked to complete aerobic and strength testing before and after the exercise program. Participants will be asked to answer questionnaires throughout the program. The at-home exercise will last for 12 weeks.

NCT ID: NCT06359821 Enrolling by invitation - Clinical trials for Metastatic Prostate Cancer

Evaluate Safety, Whole-Body Distribution and Radiation Dosimetry in Metastatic Castration Resistant Prostate Cancer

Start date: May 17, 2024
Phase: Early Phase 1
Study type: Interventional

A Study to Evaluate Safety, Whole-Body Distribution and Radiation Dosimetry of ZA-001, an Alpha-particle-emitting (At211) Radiopharmaceutical, in metastatic castration resistant prostate cancer

NCT ID: NCT06350825 Recruiting - Clinical trials for Metastatic Prostate Cancer

Cytoreductive Prostatectomy Combined With Triple or Dual Systemic Therapy in mHSPC Patients

Start date: January 1, 2016
Phase: Phase 3
Study type: Interventional

To evaluate: The radiographic progression-free survival (rPFS) of metastatic hormone-sensitive prostate cancer (mHSPC) patients treated with androgen deprivation therapy (ADT) + second-generation antiandrogens±chemotherapy combined with cytoreductive prostatectomy (CRP)

NCT ID: NCT06329830 Not yet recruiting - Clinical trials for Metastatic Castration-resistant Prostate Cancer

177Lu-PSMA, Niraparib/AA Plus Prednisone for Prostate Cancer

LUNAAR
Start date: May 2024
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this research study is to test the safety and possible side effects of Lutetium-177 (177Lu)-Prostate-Specific Membrane Antigen (PSMA)-617 along with niraparib and abiraterone acetate plus prednisone when it is given to people diagnosed with metastatic castration-resistant prostate cancer (prostate cancer that has spread to other parts of the body and does not improve with hormonal therapies) at different dose levels. Once an optimal dose is selected, the researchers want to find out what how well these treatments work to improve survival and control the growth of the tumor.

NCT ID: NCT06303713 Recruiting - Prostate Cancer Clinical Trials

LuCarbo - a Study of 177Lu-PSMA-617 Plus Carboplatin in Metastatic Castrate-resistant Prostate Cancer

Start date: May 22, 2024
Phase: Phase 1
Study type: Interventional

The purpose of this study is to see whether the combination of a chemotherapy drug, carboplatin, along with the radioligand treatment, 177Lu-PSMA-617, is safe in treating prostate cancer and whether the combination is effective in shrinking or preventing growth of prostate cancer. The names of the study drugs used in this research study are: - Carboplatin (A type of chemotherapy) - 177Lu-PSMA-617 (A type of radioligand therapy)

NCT ID: NCT06267729 Recruiting - Clinical trials for Metastatic Prostate Cancer

Study of AZD0754 in Participants With Metastatic Prostate Cancer

APOLLO
Start date: March 12, 2024
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety, tolerability, and antitumour activity of AZD0754 CAR T-cell therapy in participants with metastatic prostate cancer.

NCT ID: NCT06177015 Recruiting - Clinical trials for Metastatic Prostate Cancer

Intermittent Darolutamide Treatment in the Triple Therapy of mHSPC

Start date: December 11, 2023
Phase: Phase 3
Study type: Interventional

To evaluate the efficacy and safety of intermittent use of darolutamide compared to long-term use in combination with ADT and docetaxel in the treatment of mHSPC patients.

NCT ID: NCT06112990 Recruiting - Clinical trials for Metastatic Prostate Cancer

Creatine Supplementation and Resistance Training to Preserve Muscle Mass and Attenuate Cancer Progression

CREATINE-52
Start date: November 9, 2023
Phase: Phase 3
Study type: Interventional

The goal of this clinical trial is to test the use of creatine monohydrate supplementation with resistance training to preserve muscle mass and help lessen prostate cancer progression. The main question it aims to answer is if this treatment will help maintain muscle mass to help in reducing fatigue and improving physical function, independence, and quality of life. Participants will be asked to participate in a 52-week exercise intervention consisting of a twice weekly telehealth resistance training program.

NCT ID: NCT06062745 Not yet recruiting - Clinical trials for Metastatic Prostate Cancer

Pilot Study for Detection of PSMA-Low CRPC-NE Tumors With Fluciclovine PET/CT

Start date: February 2024
Phase: Phase 1
Study type: Interventional

This research study is studying a positron emission tomography (PET) agent called 18F-fluciclovine to evaluate how well 18F-fluciclovine-PET scans determine the extent of advanced prostate cancer that either has low prostate-specific membrane antigen (PSMA) expression or has neuroendocrine features. The name of the study interventions are: - 18F-fluciclovine-PET/CT scan - Two research blood collections