Study identifier:D9735C00001
ClinicalTrials.gov identifier:NCT07611110
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase III, Multicentre, Randomised Controlled Study to Evaluate the Efficacy and Safety of AZD2265 (FPI-2265) ²²⁵Ac-PSMA-I&T Compared With Standard of Care in Patients with PSMA-positive Metastatic Castration-resistant Prostate Cancer (VECTRA-01)
metastatic castration-resistant prostate cancer
Phase 3
No
AZD2265, Cabazitaxel, Abiraterone, Enzalutamide, Apalutamide, Darolutamide, Rezvilutamide, Radium-223
Male
670
Interventional
18 Years - n/a
Allocation: Randomized
Endpoint Classification: -
Intervention Model: Parallel Assignment
Masking: -
Primary Purpose: Treatment
Verified 01 May 2026 by AstraZeneca
AstraZeneca
-
No locations available
| Arms | Assigned Interventions |
|---|---|
| Experimental: Arm A AZD2265 | Drug: AZD2265 IV Other Name: FPI-2265 |
| Active Comparator: Arm B Investigator’s choice of cabazitaxel, ARPI switch, or radium-223 | Drug: Cabazitaxel IV in combination with oral prednisone/prednisolone Other Name: Jevtana Drug: Abiraterone Oral in combination with prednisone/prednisolone Other Name: Zytiga Drug: Enzalutamide Oral Other Name: Xtandi Drug: Apalutamide Oral Other Name: Erleada Drug: Darolutamide Oral Other Name: Nubeqa Drug: Rezvilutamide Oral Other Name: Ariane Drug: Radium-223 IV Other Name: Xofigo |