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

About This Trial

  • This study looks at existing medical records to learn how adults with advanced prostate cancer respond to treatments in everyday clinical practice.
  • It focuses on patients whose cancer has spread and who have already received hormone therapy, chemotherapy, and a targeted radiation therapy.
  • Because this is an observational study that reviews health data, it does not involve taking a new medication or attending extra clinic visits.
  • Instead, the goal is to help doctors better understand which treatment approaches work best after these standard therapies have been completed.

More Information

  • 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.

Who Can Enroll

  • Age Range: 18 - 115 years
  • Gender: Male
  • Who This Trial is For: This study looks at existing medical records to learn how adults with advanced prostate cancer respond to treatments in everyday clinical practice.

Study Details

  • Start Date: June 30, 2026
  • Lead Sponsor: Novartis Pharmaceuticals
Full Eligibility Criteria

Inclusion Criteria

  • Evidence of 177Lu-PSMA-617 use on or after 01 January 2021.
  • Evidence of treatment with ≥1 ARPI, before 177Lu-PSMA-617.
  • Evidence of treatment with ≥1 taxane, before or after 177Lu-PSMA-617.
  • Diagnosis of mCRPC prior to or on the index date. The index date is the date of the last treatment administration of the latest of an ARPI, taxane, and 177Lu-PSMA-617.
  • Age ≥18 years at index.

Exclusion Criteria

• None.

View Trial Locations and Contact Information (opens in new tab)