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OncoMatch/Clinical Trials/NCT06441994

Clinical Trial of Targeted Alpha Therapy Using [At-211]PSMA-5 for Prostate Cancer

Is NCT06441994 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies PSW-1025 for prostate cancer.

Phase 1RecruitingOsaka UniversityNCT06441994Data as of May 2026

Treatment: PSW-1025PSW-1025 is administered intravenously to patients with castration-resistant prostate cancer to evaluate its tolerability, safety, pharmacokinetics, absorbed dose, and efficacy, as well as to determine the recommended dose for Phase II.

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Extracted eligibility criteria

Cancer type

Prostate Cancer

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

Min 1 prior line

Must have received: androgen receptor signaling inhibitor (enzalutamide, apalutamide, dalortamide)

Inhibitors of androgen receptor signaling (enzalutamide, apalutamide, dalortamide, etc.)

Must have received: CYP17 inhibitor (abiraterone acetate)

Inhibitors of Cytochrome P450 17 (CYP 17) (abiraterone acetate)

Cannot have received: systemic antitumor therapy

Exception: excluding androgen receptor signaling inhibitors

Patients who received systemic antitumor therapy (e.g. chemotherapy, immunotherapy, biologic therapy such as monoclonal antibodies, excluding androgen receptor signaling inhibitors) within 4 weeks before enrollment

Cannot have received: radioligand therapy (radium chloride (Radium, 223Ra), 177Lu (Lutetium)-PSMA-617)

Patients who received radium chloride (Radium, 223Ra) or 177Lu (Lutetium)-PSMA-617 within 6 months before registration

Cannot have received: cytotoxic chemotherapy

Patients currently receiving treatment with other cytotoxic chemotherapy

Cannot have received: immunotherapy

Patients currently receiving treatment with other...immunotherapy

Cannot have received: radioligand therapy

Patients currently receiving treatment with other...radioligand therapy

Cannot have received: PARP inhibitor

Patients currently receiving treatment with...poly adenosine diphosphate-ribose polymerase (PARP) inhibitors

Cannot have received: AKT inhibitor

Patients currently receiving treatment with...AKT inhibitors

Cannot have received: investigational drug

Patients who received other investigational drugs within 5 weeks prior to enrollment

Lab requirements

Cardiac function

no clinically significant abnormal findings in electrocardiogram

Patients with no clinically significant abnormal findings in electrocardiogram, respiratory rate, and blood oxygen saturation within 30 days before the enrollment

Structured fields extracted by AI. May contain errors — verify against the official protocol.

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