Radium-223 in Combination With Enzalutamide

NCT02225704 | Completed Phase 2

• 1 other identifier: CTRIAL (ICORG) 13-21
• Study Type: interventional
• Target: 45
• Locations: 1 country
• Sites: 7

Brief Summary

This study aims to determine the safety and tolerability of Radium-223 when administered in combination with enzalutamide in progressive metastatic castrate-resistant prostate cancer.

Conditions

Prostate Cancer

Outcome Measures

Primary Outcomes (1)

• To determine safety

  To record the incidence of grade 3 or higher adverse events during the period of combination therapy; graded according to the NCI CTCAE version 4

  approximately 6 to 9 months

Secondary Outcomes (5)

• Time to clinical and Prostate Specific Antigen (PSA) progression

  Approximately 2 years

• PSA response

  approximately 2 years

• Time to first skeletal-related event

  approximately 2 years

• Pain assessment

  approximately 6 - 9 months

• Measure overall survival

  approximately 2 years

Study Arms (1)

Radium-223 and enzalutamide

EXPERIMENTAL

Radium-223 50kBq/kg by intravenous injection on day 1 of every 4 week cycle for maximum of 6 cycles Enzalutamide 160mg orally daily

Drug: Radium-223 and enzalutamide

Interventions

Radium-223 and enzalutamide DRUG

Radium-223 and enzalutamide

Eligibility Criteria

• Age: 18 Years+
• Sex: male
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Written informed consent obtained prior to any study-related procedures
• Age ≥18 years and male.
• ECOG performance status ≤ 2.
• Histologically/cytologically confirmed adenocarcinoma of the prostate, and without neuroendocrine differentiation or small cell histology.
• Metastatic disease as confirmed by Computed tomography (CT)/ Magnetic resonance imaging (MRI) or bone scan.
• \. Patients must have documented Progressive disease (PD) either by radiographic or PSA criteria as defined in a) and b) below:
• For the Radiographic PD assessment, 2 sets of scans using the same imaging modality (ie CT/MRI or bone scan) and taken at separate time points are required to document radiographic disease progression during or following the patient's most recent anti-neoplastic therapy, (note: the 1st bone scan can be from before most recent therapy but the 2nd scan must show disease progression during or after the most recent therapy).
• For patients with bone disease, progression will be assessed following recommendations by the Prostate Cancer Working Group (PCWG2, see Appendix FC): appearance of 2 or more new lesions on bone scan, confirmed, if necessary, by other imaging modalities (such as CT scan or MRI), if results of the bone scans are ambiguous).
• For patients with soft tissue lesions progression will be assessed using RECIST 1.1 criteria, (see Appendix GD). Patients may have measurable or non-measurable disease according to RECIST criteria version 1.1 (see Appendix GD)
• PSA progression is defined as an increase in PSA, as determined by 2 separate measurements taken at least 1 week apart and confirmed by a third. If the third measurement is not greater than the second measurement, then a fourth measurement must be taken and must be greater than the second measurement for the patient to be eligible for the study. Furthermore, the confirmatory PSA measurement (i.e. the third or, if applicable, fourth PSA measurement) must be defined. If a patient has received prior anti-androgen therapy (e.g. bicalutamide), PSA progression must be evident and documented after discontinuation of anti-androgen therapy, (note: The 1st PSA reading taken to document disease progression when the patient presents can be while the patient is on Casodex or other ADT).
• Prior surgical castration or concurrent use of an agent for medical castration with testosterone at screening less than 50ng/dL.
• Screening PSA ≥ 2 ng/mL.
• Patients, even if surgically sterilized who (i.e. status post-vasectomy):
• will abstain from intercourse
• or must agree to use barrier contraception during and for 6 months after discontinuation of study treatment.

You may not qualify if:

• Patients should not be receiving any other investigational agents (within 30 days prior to registration)
• Patients with Gastrointestinal (GI) tract disease resulting in an inability to take oral medication, malabsorption syndrome, a requirement for IV alimentation, prior surgical procedures affecting absorption, uncontrolled inflammatory GI disease (e.g. Crohn's disease, ulcerative colitis).
• Have current active hepatic or biliary disease
• Prior therapy with orteronel, ketoconazole, aminoglutethimide, abiraterone or enzalutamide
• All anti-androgen therapy (including bicalutamide) is excluded within 6 weeks prior to first dose of study drug. Any other therapies for prostate cancer, other than GnRH analogue therapy, such as progesterone, medroxyprogesterone, progestins (megesterol), or 5-alpha reductase inhibitors (eg, finasteride or dutasteride), must be discontinued 2 weeks before the first dose of study drug. \[Bisphosphonates and Denosumab are allowed concomitant medications\].
• Prior chemotherapy for prostate cancer with the exception of:
• neoadjuvant/ adjuvant therapy as part of initial primary treatment for local disease that was completed 2 or more years prior to screening.
• Patients who received prior docetaxol for castrate sensitive metastatic prostate cancer commencing with 120 days of ADT initation where total dose received did not exceed 450mg/m2
• Prior exposure to bone directed radioisotope therapy, eg samarium 153, strontium 90;
• Exposure to external beam radiation within 4 weeks prior to receiving the first dose of study drug. In patients with untreated imminent or established spinal cord compression, treatment with standard of care, as clinically indicated, should be completed before starting treatment with Ra-223 dichloride (Xofigo®).
• Diagnosis of or treatment for another systemic malignancy within 2 years before the first dose of study drug, or previously diagnosed with another malignancy and have any evidence of residual disease.
• History of myocardial infarction, unstable symptomatic ischemic heart disease/ unstable angina, uncontrolled on-going arrhythmias of Grade \>2 , pulmonary embolism, or any other cardiac condition within 6 months prior to first dose of study drug.
• New York Heart Association Class III or IV heart failure.
• History of seizure, underlying brain injury with loss of consciousness, stroke, transient ischaemic attack (TIA), cerebral vascular accident, primary brain tumours or brain metastases, brain arteriovenous malformation, alcoholism., or the use of concomitant medications that may lower the seizure threshold.
• Known human immunodeficiency virus (HIV) infection, active chronic hepatitis B or C, life-threatening illness unrelated to cancer, or any ongoing serious medical or psychiatric illness that could, in the investigator's opinion, potentially interfere with participation in this study. Patients will be tested for hepatitis B or C or HIV infection during screening if they are considered by the investigator to be at higher risk for these infections and have not been previously tested, or if testing is required by the independent ethics committee or institutional review board.

Sponsors & Collaborators

• Cancer Trials Ireland: lead

Study Sites (7)

Cork University Hospital

Cork, Ireland

Location

Mater Misericordiae University Hospital

Dublin, Ireland

Location

Mater Private Hospital

Dublin, Ireland

Location

SLRON, St James's Hospital

Dublin, Ireland

Location

St Vincents University Hospital / AMNCH

Dublin, Ireland

Location

Tallaght Hospital

Dublin, Ireland

Location

Galway University Hospital

Galway, Ireland

Location

MeSH Terms

Conditions

Prostatic Neoplasms

Interventions

Radium-223; enzalutamide

Condition Hierarchy (Ancestors)

Genital Neoplasms, Male; Urogenital Neoplasms; Neoplasms by Site; Neoplasms; Genital Diseases, Male; Genital Diseases; Urogenital Diseases; Prostatic Diseases; Male Urogenital Diseases

Study Officials

• Ray McDermott, Prof

  St Vincent's University Hospital / AMNCH

  PRINCIPAL INVESTIGATOR

Study Design

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

Study Record Dates

• First Submitted: August 22, 2014
• First Posted: August 26, 2014
• Study Start: June 3, 2015
• Primary Completion: July 1, 2017
• Study Completion: November 23, 2021
• Last Updated: April 13, 2026

Record last verified: 2026-04

Locations

IE (7)