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Prostatic Neoplasms clinical trials

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NCT ID: NCT06190899 Recruiting - Prostate Cancer Clinical Trials

Gedatolisib in Combination With Darolutamide in Metastatic Castration-Resistant Prostate Cancer

Start date: January 1, 2024
Phase: Phase 1/Phase 2
Study type: Interventional

This is a Phase 1/2, open-label, randomized, dose finding and dose expansion study to evaluate the safety, preliminary efficacy, and PK of gedatolisib in combination with darolutamide in subjects with mCRPC.

NCT ID: NCT06184464 Recruiting - Clinical trials for Prostate Adenocarcinoma

Prostatic Size Reduction Following of Leuprorelin Acetate

PROSTSIZE
Start date: February 2, 2024
Phase:
Study type: Observational

To determine the possible reduction in prostate size following the administration of Leuprelin prior to the application of radiotherapy.

NCT ID: NCT06178354 Recruiting - Clinical trials for Stage IIIB Prostate Cancer AJCC v8

Focal Ablation With Focal Cryotherapy or HIFU for the Treatment of Men With Localized Prostate Cancer

Start date: November 9, 2023
Phase: N/A
Study type: Interventional

This clinical trial evaluates the effectiveness of focal ablation with either focal cryotherapy or high intensity frequency ultrasound for the treatment of men with localized prostate cancer. Focal cryotherapy kills tumor cells by freezing them. High intensity frequency ultrasound uses highly focused ultrasound waves to produce heat and destroy tumor cells.

NCT ID: NCT06177093 Recruiting - Prostate Cancer Clinical Trials

De-escalated Dose SBRT in Localized Prostate Cancer (DESTINATION-MRL)

Start date: December 11, 2023
Phase: N/A
Study type: Interventional

This study is a single centre feasibility trial. The trial will recruit men with intermediate risk localised prostate cancer who will all receive targeted dose (escalated/de-escalated dose directed by MRI) 5 fraction SBRT to the prostate. Trial Objectives are: 1. Primary To develop a 5 fraction de-escalated dose SBRT protocol capable of reducing side effects 2. Secondary - To assess levels of acute GU and GI toxicity (CTCAE) - To assess levels of late GU and GI toxicity (CTCAE) - To assess late sexual quality of life (expanded EPIC, IIEF-5) - To assess biochemical relapse-free survival at 2

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: NCT06173362 Recruiting - Clinical trials for Stage IV Prostate Cancer AJCC v8

Abiraterone and Prednisone or Darolutamide for the Treatment of Advanced Prostate Cancer

Start date: November 9, 2023
Phase: Phase 2
Study type: Interventional

This phase II trial compares the effects, good and/or bad of abiraterone and prednisone or darolutamide alone in treating patients with prostate cancer that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced). Androgens (male hormones) can cause the growth of prostate tumor cells. Abiraterone acetate lowers the amount of androgens made by the body. This may help stop the growth of prostate tumor cells that need androgen to grow. Darolutamide blocks the use of androgens by the tumor cells. Prednisone is used to lessen inflammation and lower the body's immune response. Researchers want to compare the side effects of standard of care (SOC) abiraterone and prednisone or darolutamide alone in treating patients with advanced prostate cancer.

NCT ID: NCT06172478 Recruiting - Prostate Cancer Clinical Trials

A Study of HER3-DXd in Subjects With Locally Advanced or Metastatic Solid Tumors

Start date: February 26, 2024
Phase: Phase 2
Study type: Interventional

This is a proof-of-concept study designed to investigate HER3-DXd monotherapy in locally advanced or metastatic solid tumors. The study is enrolling cohorts of participants with melanoma [cutaneous/acral], squamous cell carcinomas of the head and neck (SCCHN), and HER2-negative gastric cancerovarian carcinoma, cervical cancer, endometrial cancer, bladder cancer, esophageal carcinoma, pancreatic carcinoma, and prostate cancer.

NCT ID: NCT06172283 Recruiting - Prostate Cancer Clinical Trials

Intermittent Fasting in Prostate Cancer Patients Receiving Androgen Deprivation Therapy

Start date: December 5, 2023
Phase: N/A
Study type: Interventional

This is a a pilot study to assess the feasibility of intermittent caloric restriction (plus a plant-enriched diet optionally) in prostate cancer patients receiving androgen deprivation therapy. Study feasibility measures will include enrollment rate, drop-out rate and compliance with diet measured by self-reports.

NCT ID: NCT06171139 Recruiting - Prostate Cancer Clinical Trials

Tumor Genomic Pre-test Counseling Tool for Black or African-American Men With Prostate Cancer

Start date: December 1, 2023
Phase: N/A
Study type: Interventional

The overall goal of the study is to improve equitable delivery of pre-Tumor genetic testing (TGT) counseling tool for Black or African American men with metastatic prostate cancer and evaluating the tool for implementation.

NCT ID: NCT06167629 Recruiting - Prostate Cancer Clinical Trials

Monocentric Observational Study on the Diagnostic and Prognostic Role of 18F-PSMA PET (PET/CT and PET/MR) in Prostate Cancer

Start date: October 13, 2022
Phase:
Study type: Observational

The general objective of this retrospective and prospective study is to evaluate the diagnostic and prognostic role of a quantitative analysis of PET images with 18F-PSMA in all stages of the disease in patients with prostate cancer. To this end, both imaging parameters commonly used in clinical practice and the contribution of radiomic features will be investigated. The latter are quantitative features extracted from biomedical images, and are believed to be able to provide information, otherwise impossible to investigate, useful for the characterization of various pathologies. This methodology is very promising, but also recent and therefore little studied and standardized. Our objective is also to investigate how to optimize it from a purely methodological point of view.