Observational Study on Lutetium (177Lu) Vipivotide Tetraxetan to Treat Metastatic Castration Resistant Prostate Cancer
NCT ID: NCT07093801
Last Updated: 2025-12-30
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
300 participants
OBSERVATIONAL
2025-07-30
2029-03-30
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Patients diagnosed with mCRPC treated with lutetium (177Lu) vipivotide tetraxetan
Adult patients diagnosed with mCRPC eligible for and prescribed with lutetium (177Lu) vipivotide tetraxetan by the treating physician (Multidisciplinary Team).
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
3. Written informed consent must be obtained to participate to this study
18 Years
99 Years
MALE
No
Sponsors
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Novartis Pharmaceuticals
INDUSTRY
Responsible Party
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Principal Investigators
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Novartis Pharmaceuticals
Role: STUDY_DIRECTOR
Novartis Pharmaceuticals
Locations
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Novartis Investigative Site
Asti, AT, Italy
Novartis Investigative Site
Bergamo, BG, Italy
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Brescia, BS, Italy
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Catania, CT, Italy
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Cona, FE, Italy
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Foggia, FG, Italy
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Florence, FI, Italy
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Genova, GE, Italy
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Genova, GE, Italy
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Latina, LT, Italy
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Macerata, MC, Italy
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Milan, MI, Italy
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Milan, MI, Italy
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Rozzano, MI, Italy
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Palermo, PA, Italy
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Perugia, PG, Italy
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Pisa, PI, Italy
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Rionero in Vulture, PZ, Italy
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Reggio Emilia, RE, Italy
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Roma, RM, Italy
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Roma, RM, Italy
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Roma, RM, Italy
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Roma, RM, Italy
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La Spezia, SP, Italy
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Torino, TO, Italy
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Mestre, VE, Italy
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Negrar, VR, Italy
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Napoli, , Italy
Countries
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Central Contacts
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Novartis Pharmaceuticals
Role: CONTACT
Other Identifiers
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CAAA617A1IT01
Identifier Type: -
Identifier Source: org_study_id