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Quinacrine Treatment in Patients With Androgen-Independent Prostate Cancer

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00417274
Recruitment Status : Completed
First Posted : December 29, 2006
Results First Posted : April 11, 2013
Last Update Posted : April 11, 2013
Information provided by (Responsible Party):
Cleveland BioLabs

Brief Summary:
The purpose of this study is to determine whether quinacrine is effective in the treatment of Androgen-Independent Prostate Cancer.

Condition or disease Intervention/treatment Phase
Prostatic Cancer Drug: Quinacrine Phase 2

Detailed Description:

Despite a modest improvement in survival with available chemotherapy treatments, androgen-independent metastatic prostate cancer remains essentially incurable.

Several changes in gene function that characterize malignancy have been identified. For example the p53 gene in normal tissue lessens the risk of cancer through growth arrest or cell suicidal programs. Thus the silenced p53 gene present in cancer tissue contributes to the growth of the cancer. In addition when the p53 gene is silenced, a cell survival pathway, controlled by the NF-kB gene, is activated leading increased cell survival.

Quinacrine can activate p53 and inhibit NF-kB, thus reestablishing cell suicidal programs and decreasing cell survival in cancer tissue. Moreover, quinacrine is effective against several prostate tumor cell lines in vitro, and has anti-tumor effects against prostate cancer xenografts in mice.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 31 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: An Open-Label, Phase II Safety, Tolerability, Drug Level and Efficacy Trial of Quinacrine in Patients With Androgen-Independent Metastatic Prostate Cancer
Study Start Date : December 2006
Actual Primary Completion Date : May 2008
Actual Study Completion Date : May 2008

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Prostate Cancer

Arm Intervention/treatment
Experimental: Quinacrine
Uncontrolled treatment arm
Drug: Quinacrine
100 mg daily
Other Name: CBLB102

Primary Outcome Measures :
  1. Efficacy of Quinacrine, Based on Prostate Specific Antigen (PSA) Response in Patients With Androgen-independent Metastatic Prostate Cancer [ Time Frame: End of treatment ]
    Patients who achieved a complete response (CR) or a partial response (PR) to therapy were allowed to continue to receive treatment until disease progression or unacceptable toxicity occurred, until the patient discontinued treatment for another reason, or for a total of 6 months. Patients who continued to show a CR or PR or who maintained stable disease (SD) after 6 months of therapy were to be allowed to continue therapy at the investigator's discretion.

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   Male
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Patients must be males, at least 18 years of age, with pathologically confirmed adenocarcinoma of the prostate
  • Patients must have evidence of androgen-independent metastatic prostate cancer (AIMPC) following standard antiandrogen withdrawal. AIMPC will be defined as the category of patients with metastatic prostate cancer with radiologic evidence of metastases (bone scan, CT, etc.) and castrate levels of testosterone (~ 50 ng/dL).

    1. All patients must be receiving ongoing therapy to ensure testicular androgen suppression (LHRH agonists therapy or bilateral orchiectomy).
    2. All patients receiving anti-androgen therapy [e.g., flutamide (Eulexin), bicalutamide (Casodex), or nilutamide (Nilandron)] must have initiated therapy at least 3 months (90 days) prior to the Baseline visit.
  • Patients must have received prior docetaxel-based or mitoxantrone-based chemotherapy, or refused or been ineligible for chemotherapy. Previous chemotherapy treatments must be completed at least 4 week prior to Screening, and patients must not have any residual therapy-related toxicities present at Screening.
  • Patients must have evidence of disease progression defined as any of the following:

    1. New sites of metastatic disease on radiographic imaging (bone scan or CT scan of chest/abdomen/pelvis) as determined by the referring physician.
    2. PSA progression, defined as a 50% or greater rise in PSA value over a baseline level of at least 1.0 ng/mL, confirmed after an interval of at least two weeks.
  • ECOG performance status 0-2 (see Appendix 4)
  • Patients must have adequate organ and bone marrow function as defined below:

    1. Absolute neutrophil count greater than 1500/mL
    2. Platelets greater than 100,000/mL
    3. Serum creatinine less than 2.0 mg/dL
    4. Total bilirubin less than 1.5 mg/dL
    5. AST (SGOT) and ALT (SGPT) less than 2 times the ULN [less than 5 times the ULN if liver metastases are present].
  • Sexually active men whose sexual partners are women of childbearing potential must agree to use a medically acceptable form of barrier contraception or abstinence during their participation in the study and for at least six weeks after study drug discontinuation.
  • Written informed consent/HIPAA authorization must be provided prior to the performance of any study-related procedures.

Exclusion Criteria:

  • Prior allergic reactions or a history of intolerance attributed to quinacrine or other acridine derivatives
  • Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, hematological disorders, hepatic disease, or psychiatric illness/social situations that would limit compliance with study requirements.
  • Lifetime history of porphyria or psoriasis
  • Documented glucose-6-phosphate dehydrogenase deficiency
  • Lifetime history of seizure disorder (except infant febrile seizures)
  • Lifetime history of schizophrenia, bipolar disorder, or any other psychotic disorders.
  • Lifetime history of dermatitis as an allergic/toxic reaction to any medication
  • Clinical evidence of CNS metastases
  • Patients with a history of any malignancy (other than basal, squamous cell cancers and Ta bladder cancers) within 5 years of baseline visit
  • Any grade 2 sensory neuropathy
  • QTc (Bazett) >450 msec
  • Patients with NYHA class 3 or 4 failure
  • Patients with myocardial infarction or acute coronary syndrome within the previous 6 months
  • Patients who require anti-arrhythmic treatment

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00417274

Sponsors and Collaborators
Cleveland BioLabs
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Principal Investigator: Edwin Posadas, MD University of Chicago Hospitals
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Responsible Party: Cleveland BioLabs Identifier: NCT00417274    
Other Study ID Numbers: CBL-DD-05-C-H-2003
First Posted: December 29, 2006    Key Record Dates
Results First Posted: April 11, 2013
Last Update Posted: April 11, 2013
Last Verified: September 2012
Keywords provided by Cleveland BioLabs:
Cancer of Prostate
Prostate Cancer
Cancer of the Prostate
Neoplasms, Prostate
Neoplasms, Prostatic
Prostate Neoplasms
Prostatic Cancer
Androgen-Independent Prostate Cancer
Additional relevant MeSH terms:
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Prostatic Neoplasms
Genital Neoplasms, Male
Urogenital Neoplasms
Neoplasms by Site
Prostatic Diseases
Anticestodal Agents
Antiplatyhelmintic Agents
Antiparasitic Agents
Anti-Infective Agents
Antiprotozoal Agents
Antinematodal Agents
Antineoplastic Agents
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action