Ireland
--:--IST
Latest
Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: 2025 Eurostat Trade Data and Economic Impact Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: 2025 Eurostat Trade Data and Economic Impact
Recruiting Not applicable

Towards Optimal Treatment for High Risk Prostate Cancer

NCT06204341 · tracked via the Priya Life Science Netherlands tracker
Phase
Not applicable
Started
2024-01-02
Last updated
2024-09-19

Condition(s) studied

High Risk Prostate Carcinoma

Investigational drug(s) / intervention(s)

HYPOPRIME treatment

HYPOPRIME treatment: Hypo fractionated pelvic radiotherapy with boost to primary tumour in the prostate with elective lymph node irradiation and minimized androgen deprivation therapy

Study summary

The goal of this clinical trial is to combine several optimized treatments of high risk prostate cancer. The main question to answer is: is it safe to combine these optimized treatments.

* patients will be irradiated on the prostate and (elective) lymph nodes more concentrated but with fewer hospital visits (hypofractionation)
* the tumor will get a higher dose
* androgen deprivation therapy will be reduced as much al possible preventing side effects

Researchers will compare oncological outcome and toxicity.

Eligibility

Sex
MALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Men (aged ≥18 years of age) diagnosed within 6 months before inclusion with high risk prostate cancer: * T3 based on digital rectal examination AND/OR * Grade \>= 4 AND/OR * PSA \>=20 ug/L * Indication for elective lymph node irradiation (based on current clinical guidelines) OR N1 on imaging (with a maximum of 4 suspect lymph nodes) Exclusion Criteria: * Prior pelvic radiotherapy * TransUrethral Resection of the Prostate (TURP) \< 3 months ago * Prostatectomy or other primary treatment for prostate cancer (e.g. HIFU, cryotherapy, etc) * contraindications to MRI * no visible lesion on MRI in prostate for boost * no PSMA-PET scan * inflammatory bowel disease * metastatic disease (M1) * PSA \>50 * unsuitable for SBRT or WPRT * medical history of cancer other than basal cell carcinoma of the skin

Primary outcome measure(s)

  • Biochemical recurrence free survival — 5 years
    rise of PSA 2 ng/ml above nadir
  • Late gastrointestinal and genito-urinary toxicity, and erectile dysfunction — at 6 months and 2 years
    according to CTC-AE v5

Trial sites (1)

FacilityCityRegionStatus
Haaglanden Medical Centre Leidschendam South Holland Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06204341 on ClinicalTrials.gov ↗ ← All trials in the Netherlands