Hormone Sensitive Prostate Cancer

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Review clinical trials related to Hormone Sensitive Prostate Cancer. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

This Study Will Explore Whether a Combination of the Investigational Drug Mevrometostat (PF-06821497) and Enzalutamide Will Work Better Than Taking Enzalutamide Alone in Participants With mCSPC Who Are ARPI naïve.

This study will explore whether a combination of the investigational drug mevrometostat (PF-06821497) and enzalutamide will work better than taking enzalutamide alone in participants with mCSPC who are ARPI naïve and have not yet received chemotherapy in the mCSPC setting.

Participants needed: 1,000
Trial details
Phase: Phase 3Age: 18+Biological sex: MaleType: InterventionalSponsor: PfizerUpdated: Jun 30, 2026Locations: 341
Eligibility criteria

Male participants aged ≥18 years (or the minimum age of consent in accordance wi... [+4]

Any medical or psychiatric condition including recent (within the past year) or... [+9]

Status: Recruiting

PSMA-Directed Para-Aortic Radiation Therapy for Oligorecurrent Prostate Cancer

The purpose of this prostate cancer research study is to learn about: 1. Improving control of prostate cancer using radiation therapy, delivered to the para-aortic and pelvic lymph nodes, in addition to systemic androgen suppression therapy; 2. Preserving quality of life after radiation therapy; 3. Leveraging imaging results from prostate-specific membrane antigen (PSMA) positron emission tomography (PET)/computed tomography (CT) scans to evaluate and manage disease progression.

Participants needed: 34
Trial details
Phase: Phase 2Age: 18+Biological sex: MaleType: InterventionalSponsor: University of MiamiUpdated: Jun 16, 2026Locations: 1
Eligibility criteria

Histologically proven prostate adenocarcinoma [+14]

No pathological diagnosis of prostate adenocarcinoma [+16]

Status: Recruiting

Metastasis-directed Therapy for Oligorecurrent Prostate Cancer

The aim is to investigate whether the addition of short-term androgen deprivation therapy (ADT) during 1 month or short-term ADT during 6 months together with an androgen receptor targeted therapy (ARTA) to metastasis-directed therapy (MDT) significantly prolongs poly-metastatic free survival (PMFS) and/or metastatic castration-refractory prostate cancer free survival (mCRPC-FS) in patients with oligorecurrent hormone sensitive prostate cancer.

Participants needed: 873
Trial details
Phase: Phase 3Age: 18+Biological sex: MaleType: InterventionalSponsor: Universitaire Ziekenhuizen KU LeuvenUpdated: Jul 3, 2024Locations: 1
Eligibility criteria

Histologically proven initial diagnosis of prostate adenocarcinoma [+10]

Any disorder, which in the Investigator's opinion might jeopardise the participa... [+9]

Status: Recruiting

Evaluation of Clinical Outcomes of Chemotherapy or Androgen-receptor Targeting Agent (Alone or Combined) or Radiotherapy on Primary Tumor in Addition to Androgen Deprivation Therapy in HOrmone-Sensitive Metastatic Prostate Cancer Patients

The aim of this observational study is to evaluate the clinical outcomes of treatment with docetaxel, ARTA (alone or in combination) or with radiotherapy on the primary tumor for mCSPC, in an unselected population, in clinical practice

Participants needed: 3,000
Trial details
Biological sex: MaleType: ObservationalSponsor: Santa Chiara HospitalUpdated: Jun 25, 2024Locations: 3Duration: 5 Years
Eligibility criteria

histologically confirmed diagnosis of adenocarcinoma of the prostate, metastatic... [+2]

histological diagnosis other than adenocarcinoma [+2]

Status: Recruiting

Comparing the Efficacy and Safety of Rezvilutamide+ADT+Docetaxel Versus Rezvilutamide +ADT in the mHSPC

Evaluate whether the combination of Rezvilutamide and androgen deprivation therapy (ADT) with docetaxel improves overall survival (OS) in patients with metastatic hormone-sensitive prostate cancer (mHSPC) compared to the combination of Rezvilutamide and ADT.

Participants needed: 200
Trial details
Phase: Phase 3Age: 40-80Biological sex: MaleType: InterventionalSponsor: The First Affiliated Hospital with Nanjing Medical UniversityUpdated: Aug 9, 2023Locations: 1
Eligibility criteria

Males aged ≥40 years and ≤80 years. [+9]

Prior use of LHRH agonists/antagonists; second-generation androgen receptor (AR)... [+5]