🔎 Trials Near Me

Home › Prostate Cancer › NCT06780670

Open-label Study Comparing AAA817 Versus Standard of Care in the Treatment of Previously Treated PSMA-positive mCRPC Adults Who Have Disease Progressed on or After [177Lu]Lu-PSMA Targeted Therapy

RecruitingPhase 2/3

PSMAcTION: A Phase II/III, Open-label, International, Multicenter, Randomized Study of AAA817 Versus Standard of Care in the Treatment of Adult Participants With PSMA Positive Metastatic Castration-resistant Prostate Cancer Who Progressed on or After [177Lu]Lu-PSMA Targeted Therapy

Who can join

Ages 18 to 100 · Men

Full eligibility criteria
Inclusion Criteria: ∙

* adults ≥ 18 years of age.
* ECOG performance status of 0 to 2.
* histopathological and/or cytological confirmation of adenocarcinoma of the prostate.
* PSMA-positive disease as assessed by PSMA PET/CT scan using an approved PSMA imaging agent as protocol instructed,
* castrate level of serum/plasma testosterone (\< 50 ng/dL or \< 1.7 nmol/L).
* Prior treatments with an androgen receptor pathway inhibitor (ARPI) and taxane-based chemotherapy, and progressed on or after \[177Lu\]Lu-PSMA targeted therapy.
* ≥ 1 metastatic lesion that is present on screening/baseline CT, MRI, or bone scan imaging obtained ≤ 28 days prior to randomization
* eGFR as requested by the sponsor

Exclusion Criteria:

* Any investigational agents within 28 days prior to the day of randomization.
* Any 225Ac-based investigational compound used prior to the day of randomization.
* Participants with a history of CNS metastases who are neurologically unstable, symptomatic, or receiving corticosteroids for the purpose of maintaining neurologic integrity.
* Concurrent acute kidney injury (renal failure developed between 48 hours to 7 days) or chronic kidney disease (at least 3 months of ongoing renal injury)
* Baseline xerostomia ≥ Grade 2 by CTCAE v.5
* History of uncontrolled hypertension, myocardial infarction (MI), angina pectoris, or coronary artery bypass graft (CABG) within 6 months prior to ICF signature and/or clinically active significant cardiac disease
* History of lymphoproliferative disease or any known malignancy or history of malignancy of any organ system within the past 2 years (except for basal cell carcinoma or actinic keratosis that have been treated with no evidence of recurrence in the past 3 months, non-invasive malignant colon polyps that have been removed).

Other protocol-defined inclusion/exclusion criteria may apply.

About the study

This is a Phase II/III study. Patient population is adult participants with PSMA-positive mCRPC who had treatments with androgen receptor pathway inhibitor (ARPI) and taxane-based chemotherapy and progressed on or after \[177Lu\]Lu-PSMA targeted therapy.

Treatment of interest: the investigational treatment is AAA817 regardless of subsequent anti-neoplastic treatment. The control treatment is investigator's choice of Standard of Care, regardless of subsequent anti-neoplastic treatment

What is being tested

Sponsor: Novartis Pharmaceuticals · Participants: 443 · Started: Feb 27, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT06780670

Locations in the U.S.

ArizonaHonor Health Research Institute, Scottsdale
CaliforniaVA Greater LA Healthcare System, Los Angeles
Stanford University Medical Center, Palo Alto
VA Palo Alto Health Care System, Palo Alto
Sansum Clinic, Santa Barbara
Saint Johns Cancer Institute, Santa Monica
ColoradoRocky Mountain Cancer Centers, Denver
ConnecticutHartford Hospital, Hartford
FloridaBaptist Health South, Miami
AdventHealth, Orlando
GeorgiaUniversity Cancer and Blood Center LLC, Athens
Emory University, Atlanta
IllinoisUniversity of Chicago, Chicago
IndianaIndiana University, Indianapolis
KansasUniversity of Kansas Hospital, Kansas City
LouisianaEast Jefferson Hospital, Metairie
MassachusettsBeth Israel Deaconess Medical Center, Boston
Dana Farber Cancer Institute, Boston
MissouriWA Uni School Of Med, St Louis
NebraskaNebraska Cancer Specialists, Omaha
New JerseyNew Jersey Urology LLC, Voorhees Township
New YorkMount Sinai Hosp Med School, New York
Associated Med Professionals of NY, Syracuse
Montefiore Medical Center, The Bronx
OhioCentral Ohio Urology Group, Gahanna
OregonOregon Urology Institute, Springfield
PennsylvaniaFox Chase Cancer Center, Philadelphia
South CarolinaCarolina Urologic Research Center, Myrtle Beach
TexasTexas Oncology, Dallas
Urology San Antonio, San Antonio
UtahUtah Intermountain Medical Center, Murray
VirginiaVirginia Cancer Specialists, Fairfax
Onco Hemato Asso of SW Virginia, Roanoke
WashingtonFred Hutchinson Cancer Research Center, Seattle
WisconsinMedical College Of Wisconsin, Milwaukee

Conditions

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