RecruitingPhase 1NCT06636123

GZ17-6.02 in Advanced CRPC After Progression on Anti-Androgen Therapy

GZ17-6.02 in Advanced Castration-Resistant Prostate Cancer (CRPC) After Progression on Anti-Androgen Therapy

Sponsor

Virginia Commonwealth University

Enrollment

30 participants

Start Date

Feb 18, 2025

Study Type

INTERVENTIONAL

Conditions

Castration-resistant Prostate Cancer

Summary

The purpose of this clinical trial is to determine if GZ17-6.02 delays progression of castration-resistant prostate cancer.

Eligibility

Sex: MALEMin Age: 18 Years

Inclusion Criteria14

Patients diagnosed with prostate cancer and treated with androgen deprivation therapy (ADT) and at least one androgen receptor pathway inhibitor (ARPI) (eg, abiraterone, enzalutamide, apalutamide or darolutamide). Previous prostate-specific membrane antigen (PSMA)-targeted therapy or cytotoxic chemotherapy is allowed but not required.
Androgen levels ≤50 ng/dL (≤1.73 nmol/L).
Disease progression following ADT and ARPI treatment described
PSA progression over 2 assessments, defined as rising PSA values from 2 consecutive assessments with an interval of at least 7 days between assessments. PSA levels prior to study enrollment are considered and appropriate for inclusion.
Measurable disease by RECIST v1.1 on chest/abdomen/pelvis CT or evaluable disease observed on bone scan.
Eastern Cooperative Oncology Group (ECOG) performance status 0, 1, or 2
Appropriate hepatic function defined by a total bilirubin (TBL) ≤1.5 × the upper limit of normal (ULN), alanine aminotransferase (ALT) AND aspartate aminotransferase (AST) ≤3 × ULN at screening.
Appropriate kidney function defined by calculated or actual creatinine clearance ≥30 mL/min
Absolute neutrophil count (ANC) ≥ 1,500 cells/mm3.
Platelets ≥100,000 cells/mm3.
Serum hemoglobin level ≥8 g/dL.
Agree to not donate blood or sperm during the study and for 90 days after the last dose of study treatment.
Patients with sexual partners of childbearing potential must agree to use highly effective methods of contraception throughout the study
Ability to understand and the willingness to sign a written informed consent document

Exclusion Criteria20

Any investigational agent:
within 4 weeks OR within a time interval less than at least 5 half-lives of the investigational agent, whichever is shorter, before initiating study treatment.
Low PSA (≤10 ng/mL) at initial presentation (before ADT or at symptomatic progression in the castrate setting) plus high volume (≥20) bone metastases.
Simultaneous enrollment in any other cancer treatment interventional clinical trial.
Active, uncontrolled diarrhea leading to dehydration or electrolyte disturbances not controlled with oral repletion.
Grade ≥3 uncontrolled infection.
Major surgery (in the opinion of the treating investigator) ≤3 weeks before initiating study treatment.
Not having fully recovered to a grade of 1 or lower from any surgery-related adverse effects within the 3 weeks preceding the start of the study treatment.
Small cell, anaplastic, or neuroendocrine component.
Known active brain metastasis.
Known active leptomeningeal disease.
Planned ongoing treatment with other drugs thought to potentially have adverse interactions with either of the medications included in the study treatment must be discontinued ≥2 weeks prior to initiating study treatment unless otherwise noted:
Monoamine oxidase inhibitors (MAOI) use; must discontinue use 10 days prior to initiating study therapy.
Strong or moderate CYP1A2, CYP3A4 and CYP2C19 inhibitors.
Rucaparib, Olaparib and Talazoparib, due to their common findings of liver enzyme elevation.
Inability to swallow medication.
Known hypersensitivity to GZ17-6.02 components (curcumin, harmine, and isovanillin) or excipients.
Known or suspected malabsorption condition or obstruction.
Active untreated hepatitis B or C" and "Known liver cirrhosis of any cause, active nonalcoholic steatohepatitis, or nonalcoholic fatty liver disease. Note: no additional testing necessary to confirm
Medical, psychological, or social condition that, in the opinion of the investigator, may increase the patient's risk or limit the patient's adherence with study requirements

Interventions

DRUGInvestigational Agent Administration

GZ17-6.02 will be taken orally with a high-fat meal at a fixed dose of 375 mg twice daily each day of a 28-day cycle, continuing until progression or intolerable toxicity