A 2 Part Phase 2 Trial of Galeterone in the Treatment of Castration Resistant Prostate Cancer (ARMOR2)

This study is currently recruiting participants.
Verified February 2013 by Tokai Pharmaceuticals
Sponsor:
Information provided by (Responsible Party):
Tokai Pharmaceuticals
ClinicalTrials.gov Identifier:
NCT01709734
First received: October 16, 2012
Last updated: February 19, 2013
Last verified: February 2013
  Purpose

This is a Phase 2, randomized, 2 part trial that will evaluate the safety and efficacy of galeterone in castration resistant prostate cancer (CRPC) patients. This trial will enroll patients who have not yet received androgen directed hormonal therapies (e.g. TAK-700, ARN-509, ketoconazole, enzalutamide, or galeterone) for the treatment of prostate cancer (treatment naïve) as well as CRPC patients who demonstrated disease progression while on the hormonal therapy Zytiga® (abiraterone acetate).


Condition Intervention Phase
Prostate Cancer
Drug: galeterone
Phase 2

Study Type: Interventional
Study Design: Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: A Phase 2, Randomized, Two Part Trial of Galeterone in the Treatment of Castration Resistant Prostate Cancer

Resource links provided by NLM:


Further study details as provided by Tokai Pharmaceuticals:

Primary Outcome Measures:
  • Part 1 will confirm dose to be used in Part B of the study by assessing safety and efficacy by means PSA response. [ Time Frame: 3 months ] [ Designated as safety issue: Yes ]
    This study will monitor frequency and severity of adverse events and changes in laboratory values. This study will also assess changes in levels of prostate specific antigen as a measure of treatment response

  • Part 2 of this study will further assess efficacy of the dose of galeterone chosen in Part 1 of the study in terms of changes from baseline in PSA concentration and tumor response rate by RECIST criteria (v.1.1) [ Time Frame: 3 months ] [ Designated as safety issue: No ]
    RECIST will be evaluated by tumor changes measurements as seen on CT/MRI.


Estimated Enrollment: 172
Study Start Date: December 2012
Estimated Study Completion Date: September 2014
Estimated Primary Completion Date: June 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Dose Confirmation

Dose A - galeterone tablets once daily PO for three months + extension

Dose B - galeterone tablets once daily PO for three months + extension

Dose C - galeterone tablets once daily PO for three months + extension

Drug: galeterone
Other Name: TOK-001

Detailed Description:

This trial will be split into two parts. The purpose of Part 1 will be to confirm dose and target patient population and Part 2 will be expansion of the dose and patient population selected in Part 1. For eligible patients, there will be an optional extension dosing following the completion of Part 1 or Part 2 of the trial.

Obtaining of informed consent and screening may be performed up to 28 days prior to enrollment. Each patient will be able to receive his specified regimen for 3 consecutive cycles. Each cycle consists of 28 days (approximately 1 mo.). End of Cycle 3 visit assessments will be used to determine outcome and dosing may continue up to an additional 2 weeks until the results of all assessments are obtained. Eligible patients may continue treatment in an optional extension period following the completion of the primary parts of this trial.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Male
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Male age > 18 years
  2. Histologically or cytologically confirmed adenocarcinoma of the prostate (excluding neuroendocrine differentiation or small cell histology)
  3. Ongoing androgen blockade (therapy with gonadotropin-releasing hormone (GnRH) analogues, or orchiectomy) demonstrated by serum testosterone concentration of less than 50 ng/dL.
  4. Demonstration of progression while on androgen blockade (based upon PCWG2 guidelines).
  5. Eastern Cooperative Oncology Group (ECOG) Performance Status <2

Exclusion Criteria:

  1. Prior treatment with androgen directed hormonal therapies (prior abiraterone treatment allowed for some study arms)
  2. Prior chemotherapy (unless allowed for some study arms).
  3. Treatment with non-steroidal oral antiandrogens within 4 weeks of enrollment
  4. Prior use of any chronic systemic glucocorticoids .
  5. Prior radiation therapy within 3 weeks and radionuclide therapy within 8 weeks of enrollment
  6. Prior treatment with Alpharadin® (radium-223 chloride)
  7. Treatment with anti arrhythmia therapy for ventricular arrhythmia < 4 weeks prior to enrollment
  8. Treatment with Coumadin® (warfarin sodium) or other anti-coagulant therapy (except aspirin) < 4 weeks prior to enrollment
  9. Severe systemic diseases or active uncontrolled illnesses.
  10. Abnormal heart function
  11. Liver metastases
  12. Brain metastases (unless stable disease >3 mos. by scan without additional CNS-directed therapy)
  13. The patient has known allergy to any of the treatment components
  14. Any physical or mental condition or social situation that in the opinion of the Investigator may interfere with the patient's ability to comply with the trial procedures
  15. History of excessive alcohol consumption
  16. Use of any substance known to cause AME
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01709734

Locations
United States, California
San Bernardino Urological Associates Recruiting
San Bernardino, California, United States, 92404
Contact: Charity H. Hernandez, LVN     909-881-0555     charity@sburology.com    
Contact: Roxie M. Miller, LVN     909-881-0555     roxie@sburology.com    
Principal Investigator: Franklin Chu, MD            
United States, Massachusetts
Dana Farber Cancer Institute Not yet recruiting
Boston, Massachusetts, United States, 02115
Principal Investigator: Mary-Ellen Taplin, MD            
United States, Nebraska
Urology Cancer Center and GU Research Network Recruiting
Omaha, Nebraska, United States, 68130
Contact: Luke Nordquist, M.D.         drnordquist@gucancer.com    
Contact: Susan Quinn, RN, BSN, CCRC     402-991-8468     squinn@gucancer.com    
Principal Investigator: Luke Nordquist, M.D.            
United States, South Carolina
Greenville Hospital System University Medical Center Recruiting
Greenville, South Carolina, United States, 29605
Contact: Jill Cantrell, RN     864-455-3737     cantrell@ghs.org    
Principal Investigator: Joe Stephenson, MD            
United States, Texas
Texas Urology Recruiting
Carollton, Texas, United States, 75010
Contact: Kenneth Goldberg, M.D.     972-241-1222        
Principal Investigator: Kenneth Goldberg, M.D.            
United States, Washington
University of Washington/Seattle Cancer Care Alliance Not yet recruiting
Seattle, Washington, United States, 98136
Contact: Sara Teller     206-598-0854     saratell@uw.edu    
Principal Investigator: R. B. Montgomery, MD            
Sponsors and Collaborators
Tokai Pharmaceuticals
Investigators
Principal Investigator: Bruce Montgomery, M.D. University of Washington/Seattle Cancer Care Alliance
Principal Investigator: Mary Ellen Taplin, M.D. Dana-Farber Cancer Institute
  More Information

No publications provided

Responsible Party: Tokai Pharmaceuticals
ClinicalTrials.gov Identifier: NCT01709734     History of Changes
Other Study ID Numbers: TOK-200-10
Study First Received: October 16, 2012
Last Updated: February 19, 2013
Health Authority: United States: Food and Drug Administration

Keywords provided by Tokai Pharmaceuticals:
prostate cancer CRPC

Additional relevant MeSH terms:
Prostatic Neoplasms
Genital Neoplasms, Male
Urogenital Neoplasms
Neoplasms by Site
Neoplasms
Genital Diseases, Male
Prostatic Diseases

ClinicalTrials.gov processed this record on June 17, 2013