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

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexMale
Age18-115
SponsorNovartis Pharmaceuticals

About this trial

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 criteria

Qualifiers

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.

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

1,067 Participants
are grouped into 3 trial groups

Locations

This trial has no locations

Sponsors and collaborators