RecruitingNCT07677267

A Study of Real-World Characteristics, Treatment Patterns, and Outcomes Among mCRPC Patients Previously Treated With an Androgen Receptor Pathway Inhibitor, Taxane-Based Chemotherapy, and Lutetium-177 Vipivotide Tetraxetan

Real-World Characteristics, Treatment Patterns, and Outcomes Among Adults With mCRPC Previously Treated With an Androgen Receptor Pathway Inhibitor, Taxane-Based Chemotherapy, and Lutetium-177 Vipivotide Tetraxetan


Sponsor

Novartis Pharmaceuticals

Enrollment

1,067 participants

Start Date

Jun 30, 2026

Study Type

OBSERVATIONAL

Conditions

Summary

The aim of this study is to assess treatment patterns, characteristics, and clinical outcomes among adults with metastatic castration-resistant prostate cancer (mCRPC) who have previously received ≥1 androgen receptor pathway inhibitor (ARPI), ≥1 taxane, and 177Lu-PSMA-617 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

Sex: MALEMin Age: 18 YearsMax Age: 115 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a new treatment for people with prostatic neoplasms, castration-resistant. The study is currently recruiting participants at 1 location. People eligible for this study include men aged 18 Years to 115 Years.

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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Locations(1)

Novartis

East Hanover, New Jersey, United States

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NCT07677267


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