Real-world Experience With Lutetium (177Lu) Vipivotide Tetraxetan in Metastatic Castration Resistant Prostate Cancer, an Observational, Multicenter, Prospective Cohort Study
Status: Recruiting
Location: See all (17) locations...
Intervention Type: Other
Study Type: Observational
SUMMARY
The purpose of this study is to describe routine clinical practice with lutetium (177Lu) vipivotide tetraxetan on Health related quality of life (HRQoL) at baseline, on treatment, and post progression.
Eligibility
Participation Requirements
Sex: Male
Minimum Age: 18
Maximum Age: 99
Healthy Volunteers: f
View:
⁃ All patients must meet the following inclusion criteria during the identification period:
• Adult male patients diagnosed with mCRPC and initiating lutetium (177Lu) vipivotide tetraxetan by treating physician as per local label. After treatment decision enrollment is allowed before date of cycle 1 or within 2 weeks after the date of Cycle 1.
• ≥ 18 years old at the time of enrollment
• Written informed consent must be obtained prior to any data collection
• Willing to participate in Quality of Life post treatment date collection for 1 year
Locations
Other Locations
Germany
Novartis Investigative Site
RECRUITING
Aachen
Novartis Investigative Site
RECRUITING
Augsburg
Novartis Investigative Site
RECRUITING
Berlin
Novartis Investigative Site
RECRUITING
Berlin
Novartis Investigative Site
RECRUITING
Bielefeld
Novartis Investigative Site
RECRUITING
Bonn
Novartis Investigative Site
RECRUITING
Chemnitz
Novartis Investigative Site
RECRUITING
Essen
Novartis Investigative Site
RECRUITING
Halle S
Novartis Investigative Site
RECRUITING
Jena
Novartis Investigative Site
RECRUITING
Konstanz
Novartis Investigative Site
RECRUITING
Magdeburg
Novartis Investigative Site
RECRUITING
Regensburg
Novartis Investigative Site
RECRUITING
Trier
Novartis Investigative Site
RECRUITING
Tübingen
Novartis Investigative Site
RECRUITING
Ulm
Novartis Investigative Site
RECRUITING
Würzburg
Contact Information
Primary
Novartis Pharmaceuticals
novartis.email@novartis.com
+41613241111
Backup
Novartis Pharmaceuticals
Time Frame
Start Date:2024-09-04
Estimated Completion Date:2028-02-01
Participants
Target number of participants:500
Treatments
Lutetium (177Lu) vipivotide tetraxetan
Patients with mCRPC initiating lutetium (177Lu) vipivotide tetraxetan