A Study of Real-World Characteristics, Treatment Patterns, and Clinical Outcomes in Patients With Metastatic Castration-Resistant Prostate Cancer
Condition(s) studied
Study summary
The aim of this study is to assess treatment patterns, clinical outcomes, and patient characteristics among adults with metastatic castration-resistant prostate cancer (mCRPC) in the United States (US) real-world clinical practice. This study will be conducted using data extracted from the PRECISION (PRostatE Cancer dISease observatION) data platform.
Eligibility
Primary outcome measure(s)
- Number of Patients by Prior Therapies — Baseline
- Number of Patients by Number of Post-index Lines of Therapy (LOTs) — Up to approximately 5 years
- Number of Patients by Type of Therapy at Each LOT — Up to approximately 5 years
- Percentage of Patients Switching From One Type of Therapy to Another at Each LOT — Up to approximately 5 years
- Time to First-line (1L) Treatment Initiation (TTTI) — Up to approximately 5 years
Time from index date (mCRPC diagnosis) to the start of 1L treatment. - Time to Next Therapy (TTNT) for Each LOT — Up to approximately 5 years
Time from the end of each LOT to initiation of the next LOT.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Novartis | East Hanover | New Jersey | Recruiting |
More Novartis Pharmaceuticals trials in the USA
Other trials for the same condition
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 NCT07677254 on ClinicalTrials.gov ↗ ← All trials in the USA