Last updated 14 days ago
AZD2265 Compared With Standard of Care in PSMA-positive Metastatic Castration-resistant Prostate Cancer (VECTRA-01)
670 patients around the world
Available in United States, Brazil
Approximately 670 adult participants with mCRPC will be randomized to receive either
AZD2265 or standard of care treatment (investigator's choice of cabazitaxel, ARPI switch,
or radium-223). They will receive their assigned treatment until disease progression,
unacceptable toxicity, or other discontinuation criteria are met. Tumor evaluation scans
will continue after treatment discontinuation until radiographically confirmed
progression or death.
All patients will be followed for survival until the end of the study. An Independent
Data Monitoring Committee (IDMC) composed of independent experts will be convened to
monitor the safety and scientific integrity of the study.
AstraZeneca
670Patients around the world
This study is for people with
Prostate cancer
Castration resistant prostate cancer
Requirements for the patient
From 18 Years
Male
Medical requirements
- ≥ 18 years of age.Diagnosis of adenocarcinoma of prostate.Must have had prior orchiectomy and/or ongoing ADT and a castrate level of plasma/serum testosterone.Progressive mCRPC following the most recent treatment at the time of study entry, with at least 1 metastatic lesion (measurable and/or non-measurable) that is suitable for repeated assessment by CT and/or MRI and/or bone scan.Previously treated with at least 2 cycles of PSMA-directed β-emitting radioconjugate.Previously treated with at least 1 taxane-based chemotherapy regimen for either metastatic hormone-sensitive prostate cancer or CRPC.Previously treated with at least 1 ARPI (eg, enzalutamide, abiraterone, etc.).Positive PSMA PET/CT scans, obtained with PSMA ligands (⁶⁸Ga-PSMA-11 or ¹⁸F-DCFPyL).ECOG performance status of 0 to 2.Adequate organ and bone marrow function as described in study protocol.Participants must not father children or donate sperm from signing ICF, during the study intervention and for 6 months after the last dose of study intervention.Participants must use a condom from signing ICF, during study intervention, and for 6 months after the last dose of study drug, with all sexual partners.
- Prior treatment with an α-emitting molecular targeted therapeutic radioconjugate (prior treatment with radium-223 is permitted).Progression on PSMA-directed β-emitting radioconjugate prior to the administration of Cycle 3.Receipt of > 6 cycles of PSMA-directed β-emitting therapeutic RC.History of another primary malignancy, with exceptions.Persistent toxicities (CTCAE Grade ≥ 2) caused by previous anticancer therapy, with exceptions.Spinal cord compression or brain metastases unless asymptomatic, stable, and not requiring steroids for at least 4 weeks prior to start of study intervention.Clinically significant ECG abnormalities, with exceptions.
StudyVECTRA-01
SponsorAstraZeneca
Study typeInterventional
Conditions
Castration resistant prostate cancer
Requirements
From 18 YearsMale
Unique study IDclinicaltrials.gov
NCT07611110
