ADXS-504 for the Treatment of Biochemically Recurrent Prostate Cancer

Inclusion Criteria

• Histologically documented prostatic adenocarcinoma confirmed by a pathology report from prostate biopsy or a radical prostatectomy specimen
• Age >= 18 years
• Previously undergone primary therapy for prostate cancer. Salvage external beam radiation therapy (XRT) or cryotherapy following primary therapy >= 6 months prior to randomization is allowed
• A rising PSA defined as the following * If the subject’s primary therapy was radical prostatectomy (RP) (with or without adjuvant or salvage XRT), rising PSA is defined as 2 consecutive rising values above 0.1 ng/mL, each taken >= 3 weeks apart, and the last value >= 0.3 ng/mL * If the subject received other primary therapies (e.g. XRT, cryosurgery, brachytherapy), rising PSA is defined per the Phoenix definition, i.e., 2 consecutive rising values above the PSA nadir plus 2.0 ng/mL
• PSA >= 0.3 in addition to PSADT >= 4 months, PSADT will be determined from all non-zero PSA values within 12 months prior to registration. To calculate PSADT, there must be at least THREE PSA values, with at least 3 weeks between each measurement
• Eastern Cooperative Oncology Group (ECOG) performance status 0-1, or Karnofsky score >= 70%
• Testosterone >= 150 ng/dL =< 28 days of prior to registration
• Absolute neutrophil count (ANC) > 1,500 cells/mm^3
• Hemoglobin > 9.0 g/dL
• Platelet count > 100,000 cells/mm^3
• Serum creatinine < 2 x upper limit of normal (ULN)
• Serum total bilirubin < 1.5 x ULN
• Alanine aminotransferase (ALT) < 2.5 x ULN
• Aspartate aminotransferase (AST) < 2.5 x ULN
• Subject has baseline blood oxygen saturation on room air of >= 95%
• Subject has the ability to understand and the willingness to sign a written informed consent. A signed informed consent must be obtained prior to any study specific procedures
• Subject is willing and able to provide an archived biopsy specimen which may be used for correlative studies and to determine histocompatibility antigen (HLA) type
• Subject with a female partner of child-bearing potential is eligible if he agrees to follow the contraceptive guidance during the treatment period and for at least 120 days after the final dose of study treatment

Exclusion Criteria

• Subject has evidence of measurable or evaluable metastatic disease on bone or computed tomography (CT) or positron emission tomography (PET) scans performed =< 8 weeks of registration (patients with PET scan findings consistent with metastasis but who have normal conventional imaging by CT/magnetic resonance imaging (MRI)/Bone scan using standard radiographic criteria ARE eligible)
• Subject has known brain metastasis. Subjects with neurological symptoms must undergo a CT scan/magnetic resonance imaging (MRI) of the brain to exclude brain metastasis
• Subject has an active autoimmune disease requiring systemic treatment within the past 3 months, a documented history of clinically severe autoimmune disease, or a disorder that requires systemic corticosteroids or immunosuppressive agents. Subjects with vitiligo, psoriasis, alopecia or resolved childhood asthma/atopy not requiring systemic treatment would be an exception to this rule. Subjects with hypothyroidism who are stable on hormone replacement (> 10 mg daily prednisone equivalent) or Sjogren’s syndrome will not be excluded from the study
• Subject has had an allogeneic tissue/solid organ transplant
• Subject has a known history of human immunodeficiency virus (HIV) infection (HIV 1/2 antibodies)
• Subject has a known active hepatitis B (e.g., hepatitis B virus surface antigen reactive) or hepatitis C infection (e.g., hepatitis C virus ribonucleic acid [RNA] [qualitative] is detected)
• Subject has an active infection requiring systemic therapy or is dependent on or currently receiving antibiotics that cannot be discontinued before dosing. (Note: Subjects who discontinue an antibiotic prior to dosing must wait at least 5 half-lives after the last dose of antibiotic before receiving any study treatment)
• Subject has an implanted medical device that poses a high risk for bacterial colonization and/or that cannot be easily removed (e.g., prosthetic joints, artificial heart valves, pacemakers, orthopedic screws, metal plates, bone grafts, or other exogenous implants). NOTE: More common devices and prosthetics that include arterial and venous stents, dental and breast implants and venous access devices (e.g., Port-a-Cath or Mediport) are permitted. Sponsor must be contacted prior to consenting any subject who has any other device or implant
• Subject has a contraindication (e.g., sensitivity/allergy) to trimethoprim/ sulfamethoxazole; ampicillin; ciprofloxacin
• Subject has a contraindication to non-steroidal anti-inflammatory drugs (NSAIDs)
• Subject has a known allergy to any component of the study formulation(s)
• Subject has a history of listeriosis
• Subject has had a major surgery, open biopsy or significant traumatic injury =< 6 weeks of registration
• Subject has any other serious or uncontrolled physical or mental condition/disease that, as judged by the Investigator, could place the subject at higher risk derived from their participation in the study, could confound results of the study, or would be likely to prevent compliance with the requirements of the study
• Subject has a second primary malignancy with greater than minimal metastatic potential that has not been in remission for greater than 3 years. Examples of tumors that do not require a 3-year remission: non-melanoma skin cancer, resected melanoma in situ, or non-muscle invasive urothelial carcinoma
• Subject is on or has received gonadotrophin releasing hormone (LHRH) agonists, LHRH antagonists or oral antiandrogens within 6 months prior to study enrollment
• Subject has received oral antiandrogens within 3 months prior to study enrollment
• Subject has received agents such as 5 alpha reductase inhibitors, ketoconazole, megestrol acetate, systemic steroids, or herbal supplements that are known to affect PSA (PC-SPES, saw palmetto oil) within the past month
• Subject is currently participating in or has participated in a study of an investigational agent(s) within 4 weeks of the first dose of study treatment