AGN-Cogni.Q Acute Dose Safety and Pharmacokinetics Dose-Response in Prostate Cancer Patients

Prior treatment

• Subjects who are receiving chemotherapy, or oral TKI, or immunotherapy (checkpoint inhibitor).
• Subjects who are receiving any other investigational agents.
• Use of androgen deprivation therapy (ADT) or anti-androgen therapy including LHRH agonist, antagonist, GNRH analogs, and antiandrogens.

Other illness

• Subjects with distant metastatic cancer. Node positive prostate cancer patients are allowed after completion of treatment.
• Uncontrolled intercurrent illness that would limit compliance with study requirements.
• History of New York Heart Association Class III or IV heart failure, history of a myocardial infarction within 6 months, any uncontrolled cardiac arrhythmia, or any other cardiac related problem that would be considered a contraindication for participation in the opinion of the treating physician.

Other

• All vulnerable patient populations.
• Subjects who are taking Warfarin/Coumadin.

• Willingness and ability to give informed consent.
• Agree to comply with all study procedures and attend all study visits to the best of their ability.
• Male with age \>=40 years.
• History of prostate cancer diagnosis. Subjects with history of neuroendocrine or small cell prostate cancer will be excluded. Subjects are eligible if meet one or more of the below criteria:
  • Patients treated forprostate cancer and no detectable disease on imaging and clinical determination are eligible for enrollment, regardless of risk category.
  • Patients in the low-risk and favorable intermediate-risk groups who are not currently receiving any treatment or have declined any treatment.
• Not on concurrent androgen deprivation therapy.
• ECOG performance status 0-2.
• Life expectancy of greater than 12 months.
• Subjects must have normal liver and kidney function as defined below:
  • a) total bilirubin within normal institutional limits,
  • b) AST(SGOT)/ALT(SGPT) \< 2.5 X institutional upper limit of normal,
  • c) Creatinine within 1.5 ULN of institutional limits OR creatinine clearance \> 50 mL/min/1.73 m2 for subjects with creatinine levels above institutional normal.
  • d) Adequate bone marrow function (Hgb ≥ 9.0 g/dL, Platelets ≥ 100 x 109/L, absolute neutrophil count (ANC) of ≥ 1.5 x 109/L), except for subjects with a history of chronic benign neutropenia, where an ANC of ≥ 1.0 x 109/L are eligible.
• Subjects must agree to use two medically accepted method of contraception and must agree to continue use this method while on the trial and through at least one week after the last dose of study drug. Acceptable methods of contraception include abstinence, barrier method with spermicide, intrauterine device (IUD) known to have a failure rate of less than 1% per year, or steroidal contraceptive (oral, transdermal, implanted, or injected) in conjunction with a barrier method. Periodic abstinence (e.g., calendar, ovulation, symptothermal, post ovulation methods) withdrawal, spermicides only, or lactational amenorrhea are not acceptable methods of contraception.
• Subjects must stop the CYP3A4 and CYP2C19 strong inhibitors or inducers 2 weeks prior to the start of the study and during the study.
• Subjects currently taking herbal supplements containing AGN extract, including CognI.Q, Decursinol-50, Ache Action, Fast-Acting Joint Formula, EstroG-100/Profemin must discontinue these or any other supplements containing these products 4 weeks prior to starting study drug.