Bipolar Androgen Therapy (BAT) and Radium-223 (RAD) in Metastatic Castration-resistant Prostate Cancer (mCRPC)

NCT04704505 | Recruiting Phase 2 DMC FDA Drug

• 2 other identifiers: J2116IRB00273010
• Study Type: interventional
• Target: 47
• Locations: 2 countries
• Sites: 2

Brief Summary

This is a single-arm, multicenter open label, international, phase II study of Bipolar Androgen Therapy (BAT) plus Radium-223 (RAD) in men with metastatic castration-resistant prostate cancer (mCRPC). Men with mCRPC with progressive disease (radiographically and/or biochemically) who have been treated with gonadotropin-releasing hormone (GnRH)-analogue (LHRH agonists/antagonists) continuously or bilateral orchidectomy will be enrolled in this study. Previous antiandrogen therapies are permitted, but no more than one (such as abiraterone, enzalutamide, apalutamide, darolutamide). All patients will receive treatment with Radium-223 at a dose of 55 Kilobecquerel (kBq) per kilogram of body weight IV every 28 days, for 6 cycles, plus Testosterone Cypionate 400mg Intramuscular (IM) every 28 days, until progression or unacceptable toxicity.

Conditions

Prostate Adenocarcinoma; Metastatic Prostate Adenocarcinoma; Castration-resistant

Outcome Measures

Primary Outcomes (1)

• Radiographic progression-free survival (rPFS) of BAT-RAD

  To determine the radiographic progression-free survival (rPFS) of BAT-RAD in patients with mCRPC treated with at least one novel androgen receptor (AR) targeted treatment.

  24 months

Secondary Outcomes (10)

• PSA decline ≥ 50 percent rate (PSA50) of BAT-RAD

  24 months

• Change in alkaline phosphatase of BAT-RAD

  Baseline and then on day one of each cycle (each cycle is 28 days), up to 9 cycles

• PSA progression-free survival (PSA-PFS) of BAT-RAD

  24 months

• Time to disease progression of BAT-RAD

  24 months

• Overall survival of BAT-RAD

  24 months

Other Outcomes (1)

• Percentage of patients with somatic (tumor) or germline (inherited) mutations

  24 months

Study Arms (1)

Bipolar Androgen Therapy in addition to RADium-223 (RAD)

EXPERIMENTAL

Participants will receive Bipolar Androgen Therapy (BAT) plus Radium-223 (RAD).

Radiation: radium-223; Drug: Bipolar Androgen Therapy (BAT)

Interventions

radium-223 RADIATION

Radium-223 is an alpha-particle-emitting bone-targeted therapy. All patients will receive Treatment with Radium-223 at a dose of 55 kBq per kilogram of body weight IV every 28 days, for 6 cycles,

Bipolar Androgen Therapy in addition to RADium-223 (RAD)

Bipolar Androgen Therapy (BAT) DRUG

All Patients will receiveTestosterone Cypionate 400mg IM every 28 days, until progression or unacceptable toxicity.

Bipolar Androgen Therapy in addition to RADium-223 (RAD)

Eligibility Criteria

• Age: 18 Years+
• Sex: male
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Histologically documented adenocarcinoma of the prostate confirmed by pathology report from prostate biopsy or a radical prostatectomy specimen. If prostatic tumor is of mixed histology, \> 50% of the tumor must be adenocarcinoma.
• Bone metastases as manifested by one or more lesions on a Technetium 99m bone scan performed within 2 months of screening
• Castrate-resistant prostate cancer, in the setting of castrate levels of testosterone (≤ 50 ng/dL), defined as current or historical evidence of disease progression concomitant with surgical castration or androgen deprivation therapy (ADT), as demonstrated by two consecutive rises in PSA OR new lesions on bone scan:
• PSA progression will be defined as 2 rising PSA values compared to a reference value, measured at least 7 days apart and the second value is ≥ 2 ng/mL. Appearance of one or more new areas of abnormal uptake on bone scan when compared to imaging studies acquired during castration therapy or against the precastration studies if there was no response. Increased uptake of pre-existing lesions on bone scan does not constitute progression. It must be documented within 8 weeks of screening Documented bone lesions by the appearance of ≥ 2 new lesions by bone scintigraphy or dimensionally measurable soft tissue metastatic lesion assessed by CT or MRI.
• Serum PSA ≥ 2.0 ng/mL
• Patients must be on bone health agents, either zoledronic acid or denosumab, for at least 4 weeks before enrollment. These treatments must then be continued during the study.
• Screening Eastern Cooperative Oncology Group (ECOG) performance status ≤ 1
• Asymptomatic or minimally symptomatic disease (no opioids)
• Prior treatment with no more than one novel AR targeted drug (abiraterone, enzalutamide, darolutamide or apalutamide) is permitted, but not required. Prior first-generation AR targeted therapies such as bicalutamide or nilutamide are permitted as previous therapy and does not count as novel AR targeted therapy.
• Prior chemotherapy for hormone-sensitive prostate cancer (given ≥ 12 months prior to study entry) is allowed, but not necessary.
• Adequate bone marrow, renal and liver function (Absolute Neutrophil count \> 1,000, Platelets \>100,000, Hemoglobin ≥ 9g/dL aspartate aminotransferase/ alanine amino transferase (AST)/(ALT) within normal limits (WNL); Total Bilirubin WNL.
• No evidence (within 5 years) of prior malignancies (except successfully treated basal cell or squamous cell carcinoma of the skin).
• All patients must have tissue for genomic analysis. A biopsy of a metastatic site may be done during the screening; however, archive tissue will be allowed. Prostate tissue from prostate biopsy will be allowed.

You may not qualify if:

• The presence of known visceral metastasis, including lung, liver and brain metastases.
• Spinal cord compression, imminent long bone fracture, or any other condition that, in the opinion of the investigator, is likely to require radiation therapy and/or steroids for pain control during the active phase.
• Previous treatment with chemotherapy for mCRPC, or chemotherapy for any reason within 12 months prior to registration. (Chemotherapy in the adjuvant setting or for hormone-sensitive prostate cancer is permitted, as long as it was completed more than 6 months before registration).
• History of radiation therapy, either via external beam or brachytherapy within 28 days prior to registration.
• Systemic therapy with strontium-89, samarium-153, rhenium-186 or rhenium-188 for the treatment of bony metastases within previous 24 weeks
• Use of opioid analgesics for cancer-related pain such as oxycodone, morphine or methadone. Weak opioid analgesics such as codeine or tramadol are permitted.
• Use of experimental drug within 4 weeks of treatment.
• Patients with an intact prostate AND urinary obstructive symptoms are excluded (which includes patients with urinary symptoms from benign prostatic hyperplasia (BPH).
• Patients receiving anticoagulation therapy with warfarin are not eligible for study. Patients on other anticoagulants such as rivaroxaban, dabigatran, apixaban are permitted.
• Symptomatic nodal disease, i.e. scrotal, penile or leg edema.
• Poor medical risk due to a serious, uncontrolled medical disorder, non-malignant systemic disease, or active, uncontrolled infection or a disease that may compromise safety. Examples include, but are not limited to, diabetes, heart failure, chronic obstructive pulmonary disease (COPD), ulcerative colitis, or Crohn's disease, Paget's disease, ventricular arrhythmia, recent (within 12 months) myocardial infarction, thromboembolic events or any psychiatric disorder that prohibits obtaining informed consent. Any medical intervention, any other condition, or any other circumstance which, in the opinion of the investigator, could compromise adherence with study requirements or otherwise compromise the study's objectives.
• Evidence of disease in sites or extent that, in the opinion of the investigator, would put the patient at risk from therapy with testosterone (e.g. femoral metastases with concern over fracture risk, severe and extensive spinal metastases with concern over spinal cord compression, etc). Patients with low volume visceral metastasis are permitted at the discretion of the investigator, however bone disease must be predominant.

Sponsors & Collaborators

• Bayer: collaborator
• Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins: lead

Study Sites (2)

Amber Michalik

Baltimore, Maryland, 20707, United States

RECRUITING

Moinhos de Vento Hospital

Porto Alegre, 90560-010, Brazil

NOT YET RECRUITING

MeSH Terms

Interventions

Radium-223

Study Officials

• Pedro Isaacsson Velho, M,D

  Moinhos de Vento Hospital

  PRINCIPAL INVESTIGATOR

• Samuel Denmeade, M,D

  Sidney Kimmel Comprehensive Cancer Center at the Johns Hopkins Hospital

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Rana Sullivan, RN

CONTACT

410-614-6337; ProstateCancerClinicalTrials@live.johnshopkins.edu

Amber Michalik, BA

CONTACT

667-306-8336; ProstateCancerClinicalTrials@live.johnshopkins.edu

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: January 7, 2021
• First Posted: January 11, 2021
• Study Start: April 28, 2022
• Primary Completion (Estimated): February 1, 2028
• Study Completion (Estimated): February 1, 2029
• Last Updated: February 6, 2026

Record last verified: 2026-02

Locations

US (1); BR (1)