PULSE Registry: for Patients Receiving Lutetium (177Lu) Vipivotide Tetraxetan

NCT07484269 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 753

Last updated 2026-03-20

No results posted yet for this study

Summary

The primary objective of the study is to describe real-world drug utilisation of lutetium (177Lu) vipivotide tetraxetan among patients with metastatic prostate cancer

Conditions

Sponsors & Collaborators

Principal Investigators

  • Novartis Pharmaceuticals · Novartis Pharmaceuticals

Eligibility

Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-08-01
Primary Completion
2031-07-31
Completion
2031-07-31

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07484269 on ClinicalTrials.gov