RecruitingNCT07406282

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

Double-DARE: Analysis of Doublet and Triplet Therapy With Darolutamide and Other Androgen Receptor Pathway Inhibitors in de Novo mHSPC Patients Seen in Urology Clinics in the USA


Sponsor

Bayer

Enrollment

1,400 participants

Start Date

Jul 22, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

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 androgen receptor pathway inhibitors (ARPIs), sometimes alongside chemotherapy like docetaxel. Darolutamide is an ARPI that is approved by the FDA for treating mHSPC in a "triplet" combination with ADT and docetaxel. It is also used in a "doublet" combination with ADT alone. However, there is limited information on how darolutamide is used in real-world clinical settings for this condition, which creates a gap in knowledge for making treatment decisions. This study aims to fill that gap by analyzing real-world data from electronic medical records. The primary goal is to describe the characteristics of patients with newly diagnosed mHSPC who are treated with darolutamide (either as a doublet or triplet) in urology clinics across the US. The study will also examine drug use patterns and clinical outcomes for these patients. Additionally, the study will explore the characteristics of patients treated with other ARPIs (abiraterone acetate, enzalutamide, and apalutamide) and assess the feasibility of creating matched patient groups for future comparative research. Data will be collected retrospectively from a large network of community urology practices in the US.


Eligibility

Sex: MALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This observational study is collecting data from medical records to understand how men with newly diagnosed metastatic prostate cancer are being treated in real-world urology clinics in the US — specifically comparing darolutamide to other hormone-blocking drugs called ARPIs (androgen receptor pathway inhibitors). **You may be eligible if...** - You are a male patient 18 or older - You were newly diagnosed with metastatic hormone-sensitive prostate cancer (cancer that has spread but still responds to hormone reduction therapy) - You started an ARPI drug around the time of your diagnosis - You also started hormone-blocking therapy (ADT) and/or docetaxel around the same time **You may NOT be eligible if...** - You have a history of another cancer (other than non-melanoma skin cancer) - You received PARP inhibitors, immunotherapy, or other chemotherapy before starting the ARPI - Your cancer had already become resistant to hormone therapy Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGDarolutamide

Androgen receptor pathway inhibitor for treatment of metastatic hormone-sensitive prostate cancer

DRUGAbiraterone acetate

Androgen receptor pathway inhibitor for treatment of metastatic hormone-sensitive prostate cancer

DRUGEnzalutamide

Androgen receptor pathway inhibitor for treatment of metastatic hormone-sensitive prostate cancer

DRUGApalutamide

Androgen receptor pathway inhibitor for treatment of metastatic hormone-sensitive prostate cancer


Locations(1)

Precision Point Specialty LLC PPS Analytics, a Specialty Networks LLC Company

Cleveland, Ohio, United States

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NCT07406282


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