Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).
This page lists clinical trials related to Prostate Cancer from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 22
- Active, not recruiting: 19
- Completed: 2
- Other: 7
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT03805919 — Men at High Genetic Risk for Prostate Cancer
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 500 |
| Study Type | OBSERVATIONAL |
| Conditions | Prostatic Neoplasms |
Background:
Research studies have shown that genetic changes and family history may increase a man s risk for prostate cancer. Researchers want to follow the prostate health of men who have specific genetic changes associated with prostate cancer to help them learn more about which men are at higher risk for prostate cancer.
Objectives:
To study men with specific genetic changes and determin…
NCT04175431 — Prostate Specific Membrane Antigen (PSMA) or (FACBC) PET/CT Site-Directed Therapy for Treatment of Prostate Cancer, Flu-BLAST-PC Study
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | University of Washington |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostate Adenocarcinoma |
| Interventions | ; ; |
This phase II trial studies how well prostate specific membrane antigen (PSMA) or fluciclovine positron emission tomography (PET)/computed tomography (CT) site-directed therapy works for treating patients with prostate cancer. PSMA or fluciclovine PET/CT may detect prostate cancer early and may help to show whether patients benefit from site directed treatment to PET detected abnormalities.
NCT04765150 — Integrating Quantitative MRI and Artificial Intelligence to Improve Prostate Cancer Classification
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Jonsson Comprehensive Cancer Center |
| Enrollment | 275 |
| Study Type | OBSERVATIONAL |
| Conditions | Prostate Carcinoma |
| Interventions | ; |
This study evaluates how new magnetic resonance imaging (MRI) and artificial intelligence techniques improve the image quality and quantitative information for future prostate MRI exams in patients with suspicious of confirmed prostate cancer. The MRI and artificial intelligence techniques developed in this study may improve the accuracy in diagnosing prostate cancer in the future using less in…
NCT04706663 — Precision-Based Genomics in Prostate Cancer
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 2000 |
| Study Type | OBSERVATIONAL |
| Conditions | Prostate Cancer |
Background:
Prostate cancer is the most common cancer and the second leading cause of death in males in the United States. Researchers want to find additional gene mutations that may increase a man s risk for prostate cancer and may affect how aggressive the disease is.
Objective:
To look at gene mutations in men with prostate cancer as well as the course of their disease to better understan…
NCT05417594 — Study of AZD9574 as Monotherapy and in Combination With Anti-cancer Agents in Participants With Advanced Solid Malignancies
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | AstraZeneca |
| Enrollment | 695 |
| Study Type | INTERVENTIONAL |
| Conditions | Advanced Solid Malignancies |
| Interventions | ; ; |
This study will assess the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary efficacy of AZD9574 individually and in combination with anti-cancer agents in participants with advanced cancer that has recurred/progressed.
NCT05588128 — Prospective Monitoring of Subjects With Biochemically Recurrent Prostate Cancer Using 18FDCFPyL
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 350 |
| Study Type | OBSERVATIONAL |
| Conditions | Prostate Cancer; Biochemically Recurrent |
| Interventions |
Background:
Prostate cancer is the second leading cause of cancer-related death in American men. The disease recurs in up to 50,000 men each year after their early-stage disease was treated; however, at this stage, imaging scans are often unable to find the disease in the body. In this natural history study, researchers want to find out if a new radiotracer (18F-DCFPyL) injected before positro…
NCT05918263 — Exercise for Tumor Suppressive Impact in Men With Prostate Cancer at High-Risk of Progression on Active Surveillance: The REMOVE Trial
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Fred Hutchinson Cancer Center |
| Enrollment | 68 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostate Cancer; Prostatic Neoplasms |
| Interventions | ; |
The purpose of this study is to determine whether a 12-week, home-based, virtually supervised exercise program will slow cancer progression of prostate cancer among men with prostate cancer at high-risk of progression undergoing active surveillance.
The name of the study intervention involved in this study is:
Aerobic high-intensity interval training (HIIT) (training exercise intervention)
NCT06205316 — SBRT Versus Hypofractionated Radiotherapy for Biochemically Recurrent or Oligometastatic Prostate Adenocarcinoma
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Mayo Clinic |
| Enrollment | 118 |
| Study Type | INTERVENTIONAL |
| Conditions | Biochemically Recurrent Prostate Carcinoma; Oligometastatic Prostate Carcinoma; Recurrent Prostate Adenocarcinoma; Stage IIB Prostate Cancer AJCC v8; Stage IIC Prostate Cancer AJCC v8 |
| Interventions | ; ; |
This phase III trial tests the side effects of stereotactic body radiation therapy (SBRT) compared to hypofractionated radiotherapy for treating patients with prostate adenocarcinoma that has come back after a period of improvement (recurrent) or that has spread from where it first started (primary site) to a limited number of sites (oligometastatic). SBRT is a type of external radiation therap…
NCT06217822 — First-in-human Study of 225Ac-PSMA-Trillium (BAY 3563254) in Participants With Advanced Metastatic Castration-resistant Prostate Cancer (mCRPC)
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Bayer |
| Enrollment | 198 |
| Study Type | INTERVENTIONAL |
| Conditions | Advanced Metastatic Castration-resistant Prostate Cancer; Prostate Specific Membrane Antigen (PSMA) Expression |
| Interventions |
Researchers are looking for a better way to treat participants who have metastatic castration-resistant prostate cancer (mCRPC).
mCRPC is a cancer of the prostate (male reproductive gland found below the bladder) that has spread to other parts of the body. This type of prostate cancer does not respond to hormone treatment used to lower the level of testosterone, a male sex hormone, to prevent …
NCT06465069 — A Study of LY4052031 in Participants With Advanced or Metastatic Urothelial Cancer or Other Solid Tumors
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Eli Lilly and Company |
| Enrollment | 420 |
| Study Type | INTERVENTIONAL |
| Conditions | Metastatic Solid Tumor; Recurrent Solid Tumor; Advanced Solid Tumor; Urinary Bladder Neoplasm; Triple Negative Breast Cancer |
| Interventions |
The purpose of this study is to find out whether the study drug, LY4052031, is safe, tolerable and effective in participants with advanced, or metastatic solid tumors including urothelial cancer. The study is conducted in two parts - phase Ia (dose-escalation, dose-optimization) and phase Ib (dose-expansion). The study will last up to approximately 4 years.
NCT06915909 — Robotic Prostatectomy Artificial Intelligence Low Pressure Pain (RALP) Trial
| Status | Recruiting |
| Phase | N/A |
| Sponsor | East and North Hertfordshire NHS Trust |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostate Cancer (Adenocarcinoma); Prostate Cancer (Post Prostatectomy); Prostate Cancer Surgery; Prostate Cancers; Prostate Neoplasm |
| Interventions |
The ‘Robotic Prostatectomy Artificial Intelligence Low Pressure Pain Study Trial’ aims to assess the feasibility of being able to review operative outcomes such as pain when comparing two commonly used surgical devices for the removal of prostate cancers. The data collected will inform methodologies for future, larger, multi-center trials investigating pain in patients undergoing prostate cance…
NCT06926283 — A Study of DXC008 in Patients With Prostate Cancer and Other Solid Tumors
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Hangzhou DAC Biotechnology Co., Ltd. |
| Enrollment | 110 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostate Cancer; Other Solid Tumors; Ewing Sarcoma |
| Interventions |
This is a phase I, open-label, first-in-human clinical study designed to evaluate the safety, tolerability, MTD, DLT, RP2D, the PK characteristics, preliminary anti-tumor activity, the immunogenicity of DXC008 in patients with prostate cancer and other solid tumors such as Ewing sarcoma.
NCT06995898 — The Vanguard Study: Testing a New Way to Screen for Cancer
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 24000 |
| Study Type | INTERVENTIONAL |
| Conditions | Bladder Carcinoma; Breast Carcinoma; Colorectal Carcinoma; Esophageal Carcinoma; Gastric Carcinoma |
| Interventions | ; ; |
The Vanguard Study is a feasibility study to explore several aspects of evaluating multi-cancer detection (MCD) tests in a future definitive randomized controlled trial. An MCD test measures markers in the blood in order to screen for multiple cancers simultaneously. There is a need to understand how MCDs may work as cancer screening tools. The goal of cancer screening is to reduce the burden o…
NCT06825715 — Multilevel Intervention for Precision Oncology
| Status | Recruiting |
| Phase | N/A |
| Sponsor | VA Office of Research and Development |
| Enrollment | 2653 |
| Study Type | INTERVENTIONAL |
| Conditions | Advanced Cancers of the Prostate; Cancers of the Lung |
| Interventions |
The investigators are rolling out a 3 level intervention designed to improve the use of Precision Oncology at 8 VA medical centers. The 3 components of the intervention are 1: a short educational video for patients, 2: audit and feedback to providers on their Precision Oncology practice patterns, and 3: a change in the electronic medical record to make it easier to order and review results of P…
NCT06927635 — Stereotactic Body Radiotherapy or Standard of Care for Prostate Oligoprogressive Cancer
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | University Health Network, Toronto |
| Enrollment | 75 |
| Study Type | INTERVENTIONAL |
| Conditions | Castrate Resistance Prostate Cancer; OligoProgressive Metastatic Disease |
| Interventions | ; |
This is a single centre, interventional, randomized Phase II, two-arm prospective trial investigating if Stereotactic Body Radiotherapy (SBRT) to all sites of Oligopressive (OP) disease while remaining on current Systemic Therapy (ST) will improve biochemical control compared to Standard of Care (SoC) (which involves a change in ST) for patients with OP Castrate Resistance Prostate Cancer (CRPC).
NCT07406282 — A Study to Learn About Real-world Utilization and Outcomes of Darolutamide and Other Androgen Receptor Pathway Inhibitors (ARPIs) for Newly Diagnosed Metastatic Hormone-sensitive Prostate Cancer (de Novo mHSPC) in US Urology Clinics
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Bayer |
| Enrollment | 1400 |
| Study Type | OBSERVATIONAL |
| Conditions | Prostatic Neoplasms; Metastatic Hormone-Sensitive Prostate Cancer |
| Interventions | ; ; |
Prostate cancer is the most common non-skin cancer among men in the United States. For some men, the cancer has already spread to other parts of the body at the time of diagnosis; this is called metastatic hormone-sensitive prostate cancer (mHSPC). Treatment for mHSPC has advanced significantly, with new standards of care involving androgen deprivation therapy (ADT) combined with drugs known as…
NCT07114601 — A Study of LY4257496 in Participants With Cancer (OMNIRAY)
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Eli Lilly and Company |
| Enrollment | 421 |
| Study Type | INTERVENTIONAL |
| Conditions | Breast Neoplasms; Colorectal Neoplasms; Prostate Neoplasm; Endometrial Neoplasms; Neoplasm Metastasis |
| Interventions | ; ; |
The main purpose of this study is to evaluate safety, tolerability, and efficacy of LY4257496 alone and as part of relevant standard of care (SOC) combination therapy in participants with Gastrin-releasing Peptide Receptor (GRPR)-positive advanced cancer, including but not limited to breast, colorectal, prostate, endometrial, esophageal, gastroesophageal (GE) junction, and gastric cancer. The s…
NCT07288359 — Study of GVV858 as a Single Agent or in Combination With Endocrine Therapy in Patients With HR+/HER2- Breast Cancer and Other Advanced Solid Tumors
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Novartis Pharmaceuticals |
| Enrollment | 205 |
| Study Type | INTERVENTIONAL |
| Conditions | Advanced HR+/HER2- Breast Cancer; Advanced CCNE1-amplified Solid Tumors; Metastatic Castration-resistant Prostate Cancer |
| Interventions | ; ; |
Phase I: Characterize safety and tolerability of GVV858 as a single agent and in combination with fulvestrant or letrozole. Identify dose range for optimization/recommended dose for further clinical evaluation.
Phase II: Further characterize the safety and tolerability of GVV858 in combination with fulvestrant in patients with hormone receptor-positive/human epidermal growth factor receptor 2-…
NCT07690579 — Social, Structural, and Lifestyle Drivers of Prostate Cancer Disparities
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of California, San Francisco |
| Enrollment | 350 |
| Study Type | OBSERVATIONAL |
| Conditions | Prostate Cancer; Prostate Cancer Recurrent; Prostate Metastases |
| Interventions | ; |
Prostate Cancer (PC) is the most common non-cutaneous malignancy diagnosed and second leading cause of cancer death among men across the United States. PC among Black men accounts for a higher proportion alike of cancer diagnoses and deaths. In the prostate specific antigen (PSA)-based screening era, mortality rates improved at a similar velocity among Black and White men, but the 2- to 3-fold …
NCT07296887 — CARE Tool Study Aim 3
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Washington University School of Medicine |
| Enrollment | 430 |
| Study Type | INTERVENTIONAL |
| Conditions | Gynecologic Cancer; Prostate Cancer; Lung Cancer; Colorectal Cancer |
| Interventions | ; ; |
This study is a multi-site randomized trial to study the implementation of the CARE Tool and evaluate the CARE Tool. The CARE Tool is a web-based tool that gives people information about cancer care costs, health insurance, and resources to help with costs. Overall, the study aims to help patients with cancer overcome barriers they face navigating insurance and accessing financial resources.
NCT07689656 — A Clinical Study of [68Ga]Ga-ELI421 Injection PET Imaging in Patients With Prostate Cancer
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Union Hospital, Tongji Medical College, Huazhong University of Science and Technology |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostate Cancer |
| Interventions |
Primary Objective:
To evaluate the safety and tolerability of PET imaging following a single intravenous infusion of [⁶⁸Ga]Ga-ELI421 injection in patients with prostate cancer.
Secondary Objectives:
To evaluate the biodistribution characteristics of [⁶⁸Ga]Ga-ELI421 injection; To evaluate the radiation dosimetry characteristics of [⁶⁸Ga]Ga-ELI421 injection; To evaluate the diagnostic ef…
NCT07690917 — A Study of a New PET Scanner in People With Cancer
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Memorial Sloan Kettering Cancer Center |
| Enrollment | 90 |
| Study Type | OBSERVATIONAL |
| Conditions | Non Small Cell Lung Carcinoma NSCLC; Head and Neck Cancer; Prostate Cancer |
| Interventions | ; |
The researchers are doing this study to test the capabilities of a new total-body PET scanner called the Biograph Vision Quadra. The researchers want to learn whether this scanner can produce better PET/CT images and provide more useful imaging information than standard PET/CT scanners.
Active, Not Recruiting
NCT00352924 — Agriculture Health Study
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 89655 |
| Study Type | OBSERVATIONAL |
| Conditions | Prostate Cancer; Pesticide Exposures; Lymphoma; Multiple Myeloma |
The “Agricultural Health Study” (AHS) is a collaborative effort between the National Cancer Institute and the National Institute of Environmental Health Sciences. The U.S. Environmental Protection Agency and the National Institute for Occupational Safety and Health are providing support for a limited exposure assessment effort.
Initial data collection on a prospective cohort of 89,658 study su…
NCT00339495 — Prostate Lung Colorectal and Ovarian (PLCO) Cancer Screening Trial
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 154900 |
| Study Type | OBSERVATIONAL |
| Conditions | Cancer; Death |
The Division of Cancer Preventionl (DCP, formerly DCPC), under extramural contracts to 10 U.S. clinical centers, is evaluating the effectiveness of screening for prostate, lung, colorectal and ovarian cancer (The PLCO Trial). In 1996 the NCI Executive Committee approved the expansion of the PLCO Trial to collect additional materials and to conduct additional studies. About, 74,000 men and 74,00…
NCT01140373 — Adoptive Transfer of Autologous T Cells Targeted to Prostate Specific Membrane Antigen (PSMA) for the Treatment of Castrate Metastatic Prostate Cancer (CMPC)
| Status | Active, not recruiting |
| Phase | Phase 1 |
| Sponsor | Memorial Sloan Kettering Cancer Center |
| Enrollment | 13 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostate Cancer |
| Interventions | ; |
This is a phase I study which will test the safety of different doses of the patients own immune cells which have been changed to help recognize and destroy the cancer cells. The investigators want to find out what effects, good and/or bad, it has on the body and on the prostate cancer. The immune cells (T cells) used in this study will be the patients own immune cells. They will be removed fro…
NCT02484404 — Phase I/II Study of the Anti-Programmed Death Ligand-1 Durvalumab Antibody (MEDI4736) in Combination With Olaparib and/or Cediranib for Advanced Solid Tumors and Advanced or Recurrent Ovarian, Triple Negative Breast, Lung, Prostate and Colorectal Can…
| Status | Active, not recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 268 |
| Study Type | INTERVENTIONAL |
| Conditions | Colorectal Neoplasms; Breast Neoplasms |
| Interventions | ; ; |
Background:
- Durvalumab is a drug that may help people s immune systems respond to and kill cancer cells. Olaparib is a drug that may inhibit repairing DNA damage of cancer cells. Cediranib is a drug that may stop the blood vessel growth of cancer cells. This study has two components. In the phase 1 component of the study, researchers want to investigate how well participants tolerate the co…
NCT02465060 — Targeted Therapy Directed by Genetic Testing in Treating Patients With Advanced Refractory Solid Tumors, Lymphomas, or Multiple Myeloma (The MATCH Screening Trial)
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 6452 |
| Study Type | INTERVENTIONAL |
| Conditions | Advanced Lymphoma; Advanced Malignant Solid Neoplasm; Bladder Carcinoma; Breast Carcinoma; Cervical Carcinoma |
| Interventions | ; ; |
This phase II MATCH screening and multi-sub-trial studies how well treatment that is directed by genetic testing works in patients with solid tumors, lymphomas, or multiple myelomas that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced) and does not respond to treatment (refractory). Patients must have progressed following at leas…
NCT03431350 — A Study of Niraparib Combination Therapies for the Treatment of Metastatic Castration-Resistant Prostate Cancer
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | Janssen Research & Development, LLC |
| Enrollment | 136 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostatic Neoplasms, Castration-Resistant |
| Interventions | ; ; |
The purpose of this study is to: a) establish the recommended phase 2 dose (RP2D) and to evaluate the antitumor activity and safety of niraparib combination therapies (Combinations 1 and 2) and b) to determine the relative bioavailability of niraparib and abiraterone acetate (AA) in combination (Combination 3) in participants with metastatic castration-resistant prostate cancer (mCRPC).
NCT03976843 — Prostate Specific Membrane Antigen (PMSA)-Based PET Imaging of High Risk Prostate Cancer
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 175 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostate Cancer |
| Interventions |
Background:
People with prostate cancer usually have their cancer imaged with a CT scan and bone scan. They then have their prostate gland removed. Researchers want to test a scan that might predict if prostate cancer will return after this surgery.
Objective:
To test if a PET/CT scan before the prostate gland is removed can predict if prostate cancer will return. Also, to test if this appro…
NCT04521686 — Study of LY3410738 Administered to Patients With Advanced Solid Tumors With IDH1 or IDH2 Mutations
| Status | Active, not recruiting |
| Phase | Phase 1 |
| Sponsor | Eli Lilly and Company |
| Enrollment | 200 |
| Study Type | INTERVENTIONAL |
| Conditions | Cholangiocarcinoma; Chondrosarcoma; Glioma; Any Solid Tumor |
| Interventions | ; ; |
This is an open-label, multicenter Phase 1 study to evaluate safety, tolerability and preliminary efficacy of oral LY3410738 in patients with isocitrate dehydrogenase 1 (IDH1) arginine 132 (R132)-mutant advanced solid tumors, including but not limited to cholangiocarcinoma, chondrosarcoma, and glioma or isocitrate dehydrogenase 2 (IDH2) arginine 140 (R140) or arginine 172 (R172) mutant cholangi…
NCT04624256 — Germline DNA-Based Radiosensitivity Biomarker Influence on Toxicity Following Prostate Radiotherapy, GARUDA Trial
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Jonsson Comprehensive Cancer Center |
| Enrollment | 208 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostate Adenocarcinoma; Stage I Prostate Cancer American Joint Committee on Cancer (AJCC) v8; Stage II Prostate Cancer AJCC v8; Stage IIA Prostate Cancer AJCC v8; Stage IIB Prostate Cancer AJCC v8 |
| Interventions | ; ; |
This trial studies the changes in long-term physician-scored genitourinary toxicity achieved in prostate cancer patients eligible for stereotactic radiation therapy when both patients and physicians have access to convincing but non-validated germline signature that can characterize patients as having a low or high risk of developing toxicity after radiation therapy. The information learned fro…
NCT04689828 — 177Lu-PSMA-617 vs. Androgen Receptor-Directed Therapy in the Treatment of Progressive Metastatic Castrate Resistant Prostate Cancer
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | Novartis Pharmaceuticals |
| Enrollment | 469 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostatic Neoplasms |
| Interventions | ; ; |
The purpose of this study is to determine whether 177Lu-PSMA-617 improves the Radiographic progression-free survival (rPFS) or Overall Survival (OS) compared to a change in Androgen receptor-directed therapy (ARDT) in metastatic castrate resistant prostate cancer (mCRPC) participants that were previously treated with an alternate ARDT and not exposed to a taxane-containing regimen in the CRPC o…
NCT05502315 — Study of Cabozantinib and Nivolumab in Metastatic Castration Resistant Prostate Cancer
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | Rana McKay, MD |
| Enrollment | 47 |
| Study Type | INTERVENTIONAL |
| Conditions | Castration-resistant Prostate Cancer; Metastatic Cancer |
| Interventions | ; |
This is a multicenter, single-arm, two-stage open-label phase 2 study of the combination of cabozantinib + nivolumab in subjects with advanced castration-resistant prostate cancer (CRPC).
NCT05794906 — A Study to Compare Darolutamide Given With Androgen Deprivation Therapy (ADT) and Placebo Given With ADT in Men With Hormone Sensitive Prostate Cancer and Raise of Prostate Specific Antigen (PSA) Levels After Local Therapies
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | Bayer |
| Enrollment | 985 |
| Study Type | INTERVENTIONAL |
| Conditions | Biochemically Recurrent Prostate Cancer |
| Interventions | ; ; |
Researchers are looking for a better way to treat men at high-risk of biochemical recurrence (BCR) of prostate cancer.
BCR means that in men who had prostate cancer and were treated by either surgery and/ or radiation therapy, the blood level of a specific protein called PSA rises. PSA is a marker of prostate cancer cells activity. The PSA increase means that the cancer has come back even thou…
NCT05705921 — Standard Moderately Hypofractionated RT vs. Ultra-hypofractionated Focal Lesion Ablative Microboost in Prostate Cancer
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | The Netherlands Cancer Institute |
| Enrollment | 484 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostate Cancer |
| Interventions | ; |
EBRT is one of the standard treatment options for patients with localized PCA. Based on the outcome of randomized trials, moderately hypofractionated RT(19-25 fractions of 2.5-3.4Gy) is considered equivalent to conventional fractionated schemes with 35-39 fractions of 2Gy. A schedule of 20 fractions to a dose of 60-62Gy is adopted as standard of care for all risk-groups. Driven by the success o…
NCT06029998 — Bortezomib in Patients With Metastatic Castration-Resistant Prostate Cancer With PTEN Deletion
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | University of Utah |
| Enrollment | 22 |
| Study Type | INTERVENTIONAL |
| Conditions | Metastatic Castration-resistant Prostate Cancer |
| Interventions |
The goal of this clinical trial is to test the anti-tumor activity of bortezomib in participants with Metastatic Castration Resistant Prostate Cancer (mCRPC) with PTEN Deletion.
The main question[s] it aims to answer is if the use of bortezomib will result in a decline in PSA for participants.
Participants will receive a sub-cutaneous injection of bortezomib for up 8 cycles. Each cycle is a…
NCT06874114 — An Observational Study to Learn More About Treatment Patterns and Factors Determining the Choice of Treatment in Canadian Men With Metastatic Hormone Sensitive Prostate Cancer in Routine Medical Care
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Bayer |
| Enrollment | 700 |
| Study Type | OBSERVATIONAL |
| Conditions | Metastatic Hormone-sensitive Prostate Cancer |
This is an observational study in which only data are collected from adult Canadian men with metastatic hormone sensitive prostate cancer (mHSPC) are studied. Participants will not receive any advice on treatment or any changes to the healthcare.
Metastatic hormone sensitive prostate cancer is a cancer of the prostate gland, a male reproductive gland found below the bladder. Metastatic means t…
NCT07047118 — A Study of JSB462 (Luxdegalutamide) Plus Lutetium (177Lu) Vipivotide Tetraxetan in Patients With Metastatic Castration Resistant Prostate Cancer (mCRPC)
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | Novartis Pharmaceuticals |
| Enrollment | 138 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostatic Cancer, Castration-Resistant |
| Interventions | ; |
This Phase II study aims to evaluate the efficacy and safety of the combination of JSB462 (also known as luxdegalutamide) at 100 mg and 300 mg QD doses + lutetium (177Lu) vipivotide tetraxetan (hereafter referred as AAA617) compared with AAA617 (control) in participants with metastatic Castration Resistant Prostate Cancer (mCRPC) with prior exposure to at least 1 Androgen Receptor Pathway Inhib…
NCT07082049 — AI-LLM Communication Aid in Prostate Cancer Care (AI-CAP)
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Fudan University |
| Enrollment | 160 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostate Cancer |
| Interventions | ; ; |
The goal of this clinical trial is to evaluate the efficacy of large language model (LLM)-assisted communication on psychological distress alleviation and healthcare efficiency improvement in prostate cancer patients. The main questions it aims to answer are:
Does LLM-assisted communication reduce preoperative anxiety and negative emotion more effectively than standard care? Can LLM-assisted c…
NCT07174063 — A Phase I Study of JSB462 (Luxdegalutamide) in Japanese Patients With Metastatic Prostate Cancer
| Status | Active, not recruiting |
| Phase | Phase 1 |
| Sponsor | Novartis Pharmaceuticals |
| Enrollment | 6 |
| Study Type | INTERVENTIONAL |
| Conditions | Metastatic Prostate Cancer (mCRPC) |
| Interventions |
This Phase I study aims to evaluate the safety, tolerability and PK of JSB462 in Japanese patients with metastatic prostate cancer.
NCT07344779 — A Study to Learn How Men With Advanced Prostate Cancer Respond to Treatment With Darolutamide and Hormone Therapy, With or Without Chemotherapy, in Real-world Medical Practice
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Bayer |
| Enrollment | 1600 |
| Study Type | OBSERVATIONAL |
| Conditions | Metastatic Hormone-Sensitive Prostate Cancer |
| Interventions | ; ; |
This is an international, prospective, open-label, multicenter, multi-cohort, non-interventional observational study designed to describe the real-world effectiveness and safety of darolutamide in combination with androgen deprivation therapy (ADT), with or without docetaxel, in patients with metastatic hormone-sensitive prostate cancer (mHSPC). The study aims to enroll approximately 1,600 male…
Not Yet Recruiting
NCT07690462 — Infrared Fluorescence Staining Versus Frozen Section for Prostate Cancer Surgery
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Xiangya Hospital of Central South University |
| Enrollment | 120 |
| Study Type | OBSERVATIONAL |
| Conditions | Prostate Cancer |
This study aims to validate the accuracy of the infrared fluorescence rapid detection technique for the diagnosis of prostate biopsy specimens, and to compare it with intraoperative frozen section and conventional paraffin section (the gold standard), so as to evaluate its feasibility and value in clinical application.
NCT07686380 — IL-15 Superagonist With or Without Vaccine in Biochemically Recurrent Prostate Cancer After Previous Stereotactic Body Radiation Therapy
| Status | Not yet recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 65 |
| Study Type | INTERVENTIONAL |
| Conditions | Recurrent Prostate Cancer; Prostate Cancer |
| Interventions | ; ; |
Background:
Biochemically recurrent prostate cancer (BCR) occurs when prostate-specific antigen (PSA) levels in the blood rise after surgery or radiation. BCR affects 30,000 to 50,000 men each year. Researchers want to know if a drug (N-803) alone or combined with a vaccine (ETBX-071) can reduce PSA in BCR prostate cancer after radiation.
Objective:
To test a study drug alone and combined wi…
NCT07574541 — Multitargeted Recombinant Ad5 PSA/MUC-1/Brachyury-Based Immunotherapy (TriAdeno) Vaccine With IL-15 Superagonist N-803 in Participants With Clinically Localized Prostate Cancer Undergoing Active Surveillance
| Status | Not yet recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 52 |
| Study Type | INTERVENTIONAL |
| Conditions | Adenocarcinoma; Prostate Cancer; Neoplasms; Carcinoma; Neoplasms, Glandular and Epithelial |
| Interventions | ; |
Background:
Prostate cancer is the second most common cause of cancer-related death among men in the United States. Early-stage, low-grade prostate cancer is managed with active monitoring. However, 35% of men with this cancer will need treatment within 5 years because of tumor growth. Researchers want to know if a new vaccine that targets 3 anti-cancer proteins (TriAdeno) plus a drug (N-803) …
NCT07667400 — Docetaxel and SX-682 in Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma, Salivary Gland Carcinoma, and Advanced Prostate Cancer
| Status | Not yet recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Head and Neck Cancer; Head and Neck Squamous Cell Carcinoma; Paranasal Sinus Neoplasms; Nasopharyngeal Carcinoma; Oropharyngeal Squamous Cell Carcinoma |
| Interventions | ; |
Background:
Head and neck cancers (HNCs) account for about 5% of all cancers worldwide. They grow in the mouth, throat, nasal cavity, or salivary glands. Prostate cancer is the most common cancer in men in the United States. Survival rates for these cancers are lower than 50% if they spread to other parts of the body or return after treatment. Better treatments are needed.
Objective:
To test…
Enrolling by Invitation
NCT00102544 — Use of Tracking Devices to Locate Abnormalities During Invasive Procedures
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | National Institutes of Health Clinical Center (CC) |
| Enrollment | 3894 |
| Study Type | INTERVENTIONAL |
| Conditions | Adenocarcinoma; Prostate Neoplasms; Prostate Cancer; Renal Cell Carcinoma; Von Hippel Lindau Disease |
| Interventions |
This study will evaluate the accuracy and effectiveness of an experimental tracking device for locating abnormalities during invasive procedures, such as biopsy or ablation, that cannot easily be visualized by usual imaging techniques, such as computed tomography (CT) scans or ultrasound. Some lesions, such as certain liver or kidney tumors, small endocrine abnormalities, and others, may be har…
NCT07690306 — Development and Validation of a Non-Invasive AI Diagnostic Model for Prostate Cancer Using Multiparametric MRI and PSMA PET/CT
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | Xiangya Hospital of Central South University |
| Enrollment | 1500 |
| Study Type | OBSERVATIONAL |
| Conditions | Prostate Cancer (Diagnosis) |
Prostate cancer is one of the most common malignancies in men. Currently, due to the limited diagnostic accuracy of existing imaging tests, there is a risk of missed diagnosis or unnecessary prostate biopsy. This study aims to develop and validate a non-invasive artificial intelligence (AI) diagnostic model using two advanced imaging techniques: multiparametric MRI (mpMRI) and PSMA PET/CT. By i…
NCT07328516 — Natural History Study of Early Life Exposures in Agriculture (ELEA)
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 64277 |
| Study Type | OBSERVATIONAL |
| Conditions | Prostate Cancer; Leukemia; Breast Cancer; Melanoma; Colorectal Cancer |
Study Description:
ELEA is an observational cohort study that will collect exposure information and biospecimens from the adult children of the Agricultural Health Study (AHS) cohort (https://aghealth.nih.gov/about; Protocol OH93NCN013).
The primary hypothesis is that early life exposures, particularly those found in the agricultural environment, are associated with cancer and other adverse h…
Completed Trials
NCT03345563 — Project HERO: Health Empowerment & Recovery Outcomes
| Status | Completed |
| Phase | N/A |
| Sponsor | Rutgers, The State University of New Jersey |
| Enrollment | 113 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostate Cancer; Bladder Cancer; Kidney Cancer; Colon Cancer; Rectum Cancer |
| Interventions | ; ; |
Project HERO is a 12-week study of the efficacy of Body Mind Training (BMT, i.e. Tai Chi and Qigong in this project) for reducing fatigue in male cancer survivors. This 3-arm randomized clinical trial will examine inflammatory biology and selected gene-expression pathways that are hypothesized to contribute to the intervention’s effect.
NCT04560452 — Drug Intensive Monitoring Study of Olaparib in Clinical Practice Among Chinese Patients
| Status | Completed |
| Phase | N/A |
| Sponsor | AstraZeneca |
| Enrollment | 1018 |
| Study Type | OBSERVATIONAL |
| Conditions | Ovarian Cancer; Prostate Cancer |
This is a multi-centre, prospective, non-interventional study. The study will enrol about 860 Chinese cancer patients from around 56 sites. For OC cohort, the subjects who had received olaparib for at least one dose before study enrolment in real world practices will be enrolled ( n=800) . For PC cohort, according to the doctor’s decision, patients who have prescribed and agreed to start taking…