RecruitingRecruiting
A Study of [225Ac]Ac-AKY-2519 in Patients With Metastatic Castration-Resistant Prostate Cancer
NCT07581184 · Aktis Oncology, Inc.
In plain English
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Official title
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
About this study
This Phase 1b study consists of a dose escalation portion and a backfill portion. The dose escalation portion will investigate ascending doses of \[225Ac\]Ac-AKY-2519 across two cohorts enrolling in parallel:
* Cohort A: participants with metastatic castration-resistant prostate cancer (mCRPC) with NO prior exposure to 177Lu-PSMA-617 (PLUVICTO™) and
* Cohort B: participants with metastatic castration-resistant prostate cancer (mCRPC) with prior exposure to 177Lu-PSMA-617 (PLUVICTO™)
The backfill portion may enrich in two select dose levels from each cohort (Cohort A: mCRPC 177Lu-PSMA-617 (PLUVICTO™)-naïve; Cohort B: mCRPC 177Lu-PSMA-617 (PLUVICTO™)-experienced) to gather further information on the safety and efficacy and to determine the recommended phase 2 dose (RP2D) for each cohort.
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
Study design
Enrollment target: 138 participants
Allocation: na
Masking: none
Age groups: adult, older_adult
Timeline
Starts: 2026-06-17
Estimated completion: 2032-06
Last updated: 2026-09-15
Interventions
Drug: [225Ac]Ac-AKY-2519 (therapeutic)Drug: [64Cu]Cu-AKY-2519 (imaging)
Primary outcomes
- • Occurrence of adverse events by severity and occurrence of serious adverse events (SAEs) in participants who received [225Ac]Ac-AKY-2519 (Up to 30 days following last administration of [225Ac]Ac-AKY-2519)
- • Occurrence of dose-limiting toxicity (DLT) in mCRPC participants with and without prior 177Lu-PSMA-617 exposure (From first administration of [225Ac]Ac-AKY-2519 to the end of Cycle 1 (each cycle is 28 days))
Sponsor
Aktis Oncology, Inc. · industry
Contacts & investigators
ContactPaul Schwarzenberger, MD · contact · AKY-2519-01inquiries@aktisoncology.com · +1-857-216-8482
All locations (6)
Hoag Memorial Hospital PresbyterianRecruiting
Irvine, California, United States
Biogenix Molecular, LLCRecruiting
Miami, Florida, United States
University of Kansas Medical CenterRecruiting
Kansas City, Kansas, United States
Dana-Farber Cancer InstituteRecruiting
Boston, Massachusetts, United States
BAMF HealthRecruiting
Grand Rapids, Michigan, United States
XCancerRecruiting
Omaha, Nebraska, United States