A Study to Learn About Two Medicines (Apalutamide and Enzalutamide) in People With Metastatic Castration-sensitive Prostate Cancer (mCSPC)
Part of paid clinical trials in New York, New York.
- Sponsor
- Pfizer
- Study ID
- NCT07086651
- Status
- Completed
Conditions
- Cancer of the Prostate
- Metastatic Castration Sensitive Prostate Cancer (mCSPC)
- Prostate Cancer
- Prostate Neoplasms
Eligibility Criteria
- Sex
- MALE
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Enzalutamide — DRUGAs provided in real-world setting
- Apalutamide — DRUGAs provided in real-world setting
Study Details
The purpose of this study is to learn about how long apalutamide and enzalutamide are taken by men to treat mCSPC. Prostate cancer is one of the most common cancers in men. The prostate is a gland in the male body that helps make semen. Metastatic cancer is a cancer that has spread to other parts of the body. Castration-sensitive prostate cancer means the cancer is being controlled by keeping the testosterone levels as low as would be expected if the testicles were removed by surgery. This is a real-world study, not a clinical study. This means that researchers will look at what happens when men receive the treatments prescribed by their own doctor as part of their usual healthcare treatment. In this study, researchers will use information from cancer clinics (Flatiron Health electronic health records). The study will include patients' information from the database for men who: * Were identified to have mCSPC. * Started treatment with apalutamide or enzalutamide (index date) for mCSPC. * Were 18 years of age or older on the index date. Men in this study will be taking apalutamide or enzalutamide for treatment of their mCSPC. The study will compare how long men take apalutamide or enzalutamide. This study will use patient information from cancer clinics. Information from start of apalutamide or enzalutamide treatment until information is available in the database will be used to describe how long patients receive treatment.
Key Dates
- Start date
- Jul 21, 2025
- Status verified
- Dec 2025
- Primary completion
- Oct 31, 2025
- Completion
- Oct 31, 2025
Study Design
- Enrollment
- 1,300 participants (actual)
Arms
- Arm: Enzalutamide cohortPatients initiating enzalutamide for mCSPC
- Arm: Apalutamide cohortPatients initiating apalutamide for mCSPC
Primary Outcome Measure
Treatment duration [ Time Frame: Up to approximately 65 months ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Pfizer, Inc | New York | New York | 10001 | - |
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