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

RecruitingPhase 1

BActinium-1: A Phase 1b, Multicenter, Open-label Study to Evaluate the Safety and Efficacy of Intravenous Administration of B7-H3 Radiopharmaceutical ([225Ac]Ac-AKY-2519) in Metastatic Castration-Resistant Prostate Cancer

Who can join

Ages 18 and older · Men

Full eligibility criteria
Inclusion Criteria:

* Age ≥ 18 years
* Histologic or cytologic confirmation of prostatic adenocarcinoma
* ECOG Performance Status of 0 or 1
* Adequate end-organ function
* Ability to give informed consent and comply with study requirements
* Patients with CNS metastases are eligible if they have received therapy and are neurologically stable, asymptomatic and not receiving corticosteroids
* Castrate levels of serum testosterone (\< 50 ng/dL)
* Documented disease progression on most recent prior line of therapy, either by PSA or imaging-based progression
* Cohort B: Received 2 or more prior doses of 177Lu-PSMA-617 (PLUVICTO)

Exclusion Criteria:

* Prior treatment with more than 2 Androgen receptor pathway inhibitors (ARPIs) and/or more than 1 taxane-based therapy in the mCRPC setting
* Prior treatment with a targeted radiotherapy

  o Exception: Cohort B is required to have had at least 2 prior doses of 177Lu-PSMA-617 (PLUVICTO)
* Prior treatment with a B7-H3 targeted therapy
* Received an investigational agent within the previous 28 days
* Impaired cardiac function or clinically significant cardiac disease
* Concurrent serious medical condition that would impair study participation or impact the assessment of treatment related toxicity

About the 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™).

What is being tested

Sponsor: Aktis Oncology, Inc. · Participants: 138 · Started: Jun 17, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07581184

Locations in the U.S.

CaliforniaHoag Memorial Hospital Presbyterian, Irvine
FloridaBiogenix Molecular, LLC, Miami
KansasUniversity of Kansas Medical Center, Kansas City
MassachusettsDana-Farber Cancer Institute, Boston
MichiganBAMF Health, Grand Rapids
NebraskaXCancer, Omaha

Conditions

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