← Eichor
Study identifier: NCT07581184 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Study of [225Ac]Ac-AKY-2519 in Patients With Metastatic Castration-Resistant Prostate Cancer

Condition: Castration Resistant Metastatic Prostate Cancer · Prostate Cancer · mCRPC (Metastatic Castration-resistant Prostate Cancer)  ·  Sponsor: Aktis Oncology, Inc.

PhasePhase 1
Planned participants138
Who can joinMale, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is a Phase 1b, multi-center, open-label study to evaluate the safety, tolerability, dosimetry, and pharmacokinetics (PK) of \[64Cu\]Cu-AKY-2519 and/or \[225Ac\]Ac-AKY-2519, as well as the preliminary anti-tumor activity of \[225Ac\]Ac-AKY-2519 in participants with metastatic castration-resistant prostate cancer (mCRPC) with and without prior exposure to 177Lu-PSMA-617 (PLUVICTO™).

This description comes directly from the study's public registry record.

Talk to the study team

Tiffany Wang, MD  ·  +1-857-216-8482  ·  AKY-2519-01inquiries@aktisoncology.com

Always discuss trial participation with your own doctor first.

Locations (4)

Hoag Memorial Hospital PresbyterianIrvine, California, United StatesRecruiting
Biogenix Molecular, LLCMiami, Florida, United StatesRecruiting
BAMF HealthGrand Rapids, Michigan, United StatesRecruiting
XCancerOmaha, Nebraska, United StatesRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07581184