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AZD2265 Compared With Standard of Care in PSMA-positive Metastatic Castration-resistant Prostate Cancer (VECTRA-01)

RecruitingPhase 3

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)

Who can join

Ages 18 and older · Men

Full eligibility criteria
Inclusion Criteria:

* ≥ 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.

Exclusion Criteria:

* 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.

About the study

The intention of the study is to demonstrate superiority of AZD2265 relative to standard of care treatments by assessment of radiographic progression-free survival (rPFS) and overall survival (OS) in participants with mCRPC.

What is being tested

Sponsor: AstraZeneca · Participants: 670 · Started: May 4, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07611110

Locations in the U.S.

AlabamaResearch Site, Dothan
ArizonaResearch Site, Phoenix (Not yet recruiting)
CaliforniaResearch Site, Duarte (Not yet recruiting)
Research Site, Irvine (Not yet recruiting)
Research Site, Newport Beach
Research Site, San Francisco (Not yet recruiting)
ColoradoResearch Site, Aurora (Not yet recruiting)
FloridaResearch Site, Miami
IllinoisResearch Site, O'Fallon (Not yet recruiting)
LouisianaResearch Site, Metairie
MichiganResearch Site, Grand Rapids (Not yet recruiting)
MissouriResearch Site, St Louis (Not yet recruiting)
NebraskaResearch Site, Omaha
New MexicoResearch Site, Albuquerque (Not yet recruiting)
New YorkResearch Site, New Hyde Park (Not yet recruiting)
Research Site, New York (Not yet recruiting)
OhioResearch Site, Cleveland (Not yet recruiting)
Research Site, Dayton (Not yet recruiting)
OregonResearch Site, Portland (Not yet recruiting)
PennsylvaniaResearch Site, Pittsburgh (Not yet recruiting)
South CarolinaResearch Site, Myrtle Beach (Not yet recruiting)
TennesseeResearch Site, Nashville (Not yet recruiting)
TexasResearch Site, Houston
UtahResearch Site, Salt Lake City (Not yet recruiting)
WashingtonResearch Site, Tacoma (Not yet recruiting)

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.