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Clinical Trials in the USA / NCT05849298
Active, not recruiting Phase 2

A Phase II Study of AAA617 Alone and AAA617 in Combination With ARPI in Patients With PSMA PET Scan Positive CRPC

NCT05849298 · tracked via the Priya Life Science USA tracker
Sponsor
Novartis Pharmaceuticals
Phase
Phase 2
Started
2024-01-03
Last updated
2026-09-11

Condition(s) studied

Prostatic Neoplasm

Investigational drug(s) / intervention(s)

AAA617 →AAA517 →Piflufolastat F 18 →ARPI →ADT →Best supportive care

AAA617: Administration intravenously once every 6 weeks (1 cycle) for 6 cycles

AAA517: Single intravenous dose of approx. 150 Megabecquerel (MBq) prior PSMA-PET scans

Piflufolastat F 18: Single intravenous dose of approx. 333 Megabecquerel (MBq) prior PSMA-PET scans

ARPI: Enzalutamide, Darolutamide, Apalutamide as prescribed by the local investigator

ADT: as prescribed by the local investigator

Best supportive care: as prescribed by the local investigator

Study summary

The purpose of this study is to evaluate the efficacy and safety of AAA617 alone (Lutetium \[177Lu\] vipivotide tetraxetan) and in combination with an Androgen Receptor Pathway Inhibitors (ARPI) in participants with PSMA-positive, castration-resistant prostate cancer and no evidence of metastasis in conventional imaging (CI) (i.e., CT/MRI and bone scans).

Eligibility

Sex
MALE
Min age
18 Years
Max age
100 Years
Healthy volunteers
No
Key Inclusion criteria * Participants must be adults ≥ 18 years of age with signed informed consent prior to participation to study * Histologically or cytologically confirmed prostate cancer * Participants must have ongoing androgen deprivation therapy with a GnRH agonist/antagonist or prior bilateral orchiectomy at the time of randomization. Intermittent administration of ADT is accepted before randomization if criterion for serum testosterone is met * Castrate level of serum testosterone (\< 1.7 nmol/l \[50 ng/dl\]) on GnRH agonist or antagonist therapy (continuous/intermittent) or after bilateral orchiectomy prior to randomization * Participants must have evidence of PSMA-positive disease (N1 or M1) as seen on a AAA517 or piflufolastat F 18 PET/CT scan at baseline as determined by Blinded Independent Central Review (BICR) based on the methodology proposed in the Prostate Cancer Molecular Imaging Standardized Evaluation (PROMISE) (Eiber et al 2018). Participants with M1 disease only on PSMA PET scan are allowed to participate * Participants must have a negative conventional imaging for M1 disease. * Participants must have adequate organ functions: bone marrow reserve, hepatic \& renal Key Exclusion criteria * Prior or present evidence of metastatic disease as assessed by CT/MRI locally for soft tissue disease and whole-body radionuclide bone scan for bone disease. Exception: Participants with pelvic disease may be eligible (e.g., participants with enlarged lymph nodes below the bifurcation of common iliac arteries (N1)) * Unmanageable concurrent bladder outflow obstruction or urinary incontinence. Note: participants with bladder outflow obstruction or urinary incontinence, which is manageable with best available standard of care (incl. pads, drainage) are allowed * Active clinically significant cardiac disease; history of seizure or condition that may pre-dispose to seizure which may require treatment with surgery or radiation therapy * Prior therapy with: second generation anti-androgens (e.g., enzalutamide, apalutamide and darolutamide) \< 3 months before randomization; CYP17 inhibitors (e.g., abiraterone acetate, orteronel, galeterone) \< 3 months before randomization; ketoconazole (short duration ketoconazole treatment (\<28 days) is permitted); radiopharmaceutical agents (e.g., Strontium-89) if wash-out period of at least 3 months is not completed, PSMA-targeted radioligand therapy; immunotherapy (e.g., sipuleucel-T); chemotherapy, except if administered in the adjuvant/neoadjuvant setting, completed \> 2 years before randomization; any other investigational agents for CRPC; use of estrogens, 5-α reductase inhibitors (finasteride, dutasteride), other steroidogenesis inhibitors (aminoglutethimide) or first-generation anti-androgens (bicalutamide, flutamide, nilutamide, cyproterone) within 28 days before randomization; radiation therapy (external beam radiation therapy \[EBRT\] and brachytherapy within 28 days before randomization * Other concurrent cytotoxicity chemotherapy, immunotherapy, radioligand therapy, poly adenosine diphosphate-ribose polymerase (PARP) inhibitor, biological therapy or investigational therapy Other protocol-defined inclusion/exclusion criteria may apply.

Primary outcome measure(s)

Trial sites (31)

FacilityCityRegionStatus
Rocky Mountain Cancer Centers Denver Colorado
University Cancer and Blood Center LLC Athens Georgia
Urology Of Indiana Indianapolis Indiana
Unity Point Clinic Des Moines Iowa
Urology Cancer Center PC Omaha Nebraska
Oregon Urology Institute Springfield Oregon
Wellspan York Hospital York Pennsylvania
Univ of Texas Southwest Med Center Dallas Texas
Rio Grande Urology El Paso Texas
Houston Methodist Hospital Houston Texas
Novartis Investigative Site São Paulo São Paulo
Novartis Investigative Site São Paulo São Paulo
Novartis Investigative Site Toronto Ontario
Novartis Investigative Site Montreal Quebec
Novartis Investigative Site Montreal Quebec
Novartis Investigative Site Olomouc Czechia
Novartis Investigative Site Angers France
Novartis Investigative Site Brest France
Novartis Investigative Site Strasbourg France
Novartis Investigative Site Berlin Germany
Novartis Investigative Site Genova GE
Novartis Investigative Site Milan MI
Novartis Investigative Site Roma RM
Novartis Investigative Site Naples Italy
Novartis Investigative Site Kielce Poland
Novartis Investigative Site Singapore Singapore
Novartis Investigative Site Seoul South Korea
Novartis Investigative Site Seoul South Korea
Novartis Investigative Site L'Hospitalet de Llobregat Barcelona
Novartis Investigative Site Barcelona Spain
Novartis Investigative Site Madrid Spain

More Novartis Pharmaceuticals trials in the USA

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05849298 on ClinicalTrials.gov ↗ ← All trials in the USA