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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

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Observational
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
Participation Requirements
Sex: Male
Minimum Age: 18
Healthy Volunteers: f
View:

• Male patients with evidence of de novo mHSPC during the study period

• Initiation of ARPI therapy during the patient identification period and within ±90 days from the mHSPC diagnosis

• Age ≥18 years at index date (ARPI initiation for mHSPC)

• Initiation of ADT and/or docetaxel therapy within ±90 days from index date

• At least 90 days of EMR activity prior to the index date

• At least 90 days of EMR activity post-index, unless the patient died earlier.

Locations
United States
Ohio
Precision Point Specialty LLC PPS Analytics, a Specialty Networks LLC Company
RECRUITING
Cleveland
Contact Information
Primary
Bayer Clinical Trials Contact
clinical-trials-contact@bayer.com
(+)1-888-84 22937
Time Frame
Start Date: 2025-07-22
Estimated Completion Date: 2026-05-31
Participants
Target number of participants: 1400
Treatments
Darolutamide + ADT + docetaxel
Patients receiving darolutamide in combination with androgen deprivation therapy with docetaxel
Abiraterone acetate + ADT + docetaxel
Patients receiving abiraterone acetate in combination with androgen deprivation therapy with docetaxel
Enzalutamide + ADT
Patients receiving enzalutamide in combination with androgen deprivation therapy
Apalutamide + ADT
Patients receiving apalutamide in combination with androgen deprivation therapy
Darolutamide + ADT
Patients receiving darolutamide in combination with androgen deprivation therapy
Abiraterone acetate + ADT
Patients receiving abiraterone acetate in combination with androgen deprivation therapy
Related Therapeutic Areas
Sponsors
Leads: Bayer

This content was sourced from clinicaltrials.gov