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Effect of Zoledronic Acid in Patients With Prostate Cancer and Bone Metastasis

Primary Purpose

Prostate Cancer Patients With Bone Metastasis

Status
Completed
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Zoledronic acid
Sponsored by
Novartis Pharmaceuticals
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prostate Cancer Patients With Bone Metastasis focused on measuring Prostate cancer, Bone metastasis, Skeletal related event

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion criteria: Signed informed consent A histologically confirmed diagnosis of carcinoma of the prostate Therapy with hormonal treatments (medical or surgical castration) Patients must have objective evidence of metastatic disease to bone. Adequate liver function - serum total bilirubin concentration less than 1.5 x upper limit of normal value ECOG performance status of 0, 1 or 2 Exclusion criteria: Bone pain which requires strong narcotic therapy with centrally acting analgesic agents. More than 3 bisphosphonate applications in patients history. Previous Radiation therapy to bone (including therapeutic radioisotopes such as strontium 89) within 3 months prior to Visit 2. Abnormal renal function as evidenced by A calculated creatinine clearance < 30 ml/minute. Creatinine clearance (CrCl) is calculated using the Cockcroft-Gault formula: CrCl= [140-age (years)] x weight (kg) {x 0.85 for female patients} [72 x serum creatinine (mg/dL)] Corrected (adjusted for serum albumin) serum calcium concentration < 8.0 mg/dl (2.00 mmol/L) or ≥ 12.0 mg/dl (3.00 mmol/L) Life expectancy < 6 months Patients with evidence in the six months prior to randomization of severe cardiovascular disease (defined as uncontrolled congestive heart failure), hypertension refractory to treatment, or symptomatic coronary artery disease uncontrolled by treatment Use of other investigational drugs (drugs not marketed for any indication) within 30 days prior to the date of randomization Current active dental problems including infection of the teeth or jawbone (maxilla or mandibular); dental or fixture trauma, or a current or prior diagnosis of osteonecrosis of the jaw (ONJ), of exposed bone in the mouth, or of slow healing after dental procedures. Recent (within 6 weeks) or planned dental or jaw surgery (e.g. extraction, implants) Other protocol-defined inclusion and exclusion criteria may apply.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    ZOL446

    Arm Description

    Outcomes

    Primary Outcome Measures

    Rate of skeletal complications

    Secondary Outcome Measures

    Time to first skeletal complication
    Bone pain
    Patients´ satisfaction with treatment
    Bone turnover parameters

    Full Information

    First Posted
    October 9, 2005
    Last Updated
    March 21, 2011
    Sponsor
    Novartis Pharmaceuticals
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00237159
    Brief Title
    Effect of Zoledronic Acid in Patients With Prostate Cancer and Bone Metastasis
    Official Title
    Effect of Zoledronic Acid in Patients With Prostate Cancer and Bone Metastasis
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2011
    Overall Recruitment Status
    Completed
    Study Start Date
    October 2002 (undefined)
    Primary Completion Date
    December 2005 (Actual)
    Study Completion Date
    undefined (undefined)

    3. Sponsor/Collaborators

    Name of the Sponsor
    Novartis Pharmaceuticals

    4. Oversight

    5. Study Description

    Brief Summary
    It is the aim of this clinical study to evaluate the skeletal-related event rate and tolerability of zoledronic acid in patients with prostate cancer patients and bone metastases.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Prostate Cancer Patients With Bone Metastasis
    Keywords
    Prostate cancer, Bone metastasis, Skeletal related event

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 4
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    Non-Randomized
    Enrollment
    284 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    ZOL446
    Arm Type
    Experimental
    Intervention Type
    Drug
    Intervention Name(s)
    Zoledronic acid
    Other Intervention Name(s)
    ZOL446
    Primary Outcome Measure Information:
    Title
    Rate of skeletal complications
    Time Frame
    3 months
    Secondary Outcome Measure Information:
    Title
    Time to first skeletal complication
    Time Frame
    3 months
    Title
    Bone pain
    Time Frame
    3 months
    Title
    Patients´ satisfaction with treatment
    Time Frame
    3 months
    Title
    Bone turnover parameters
    Time Frame
    3 months

    10. Eligibility

    Sex
    Male
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion criteria: Signed informed consent A histologically confirmed diagnosis of carcinoma of the prostate Therapy with hormonal treatments (medical or surgical castration) Patients must have objective evidence of metastatic disease to bone. Adequate liver function - serum total bilirubin concentration less than 1.5 x upper limit of normal value ECOG performance status of 0, 1 or 2 Exclusion criteria: Bone pain which requires strong narcotic therapy with centrally acting analgesic agents. More than 3 bisphosphonate applications in patients history. Previous Radiation therapy to bone (including therapeutic radioisotopes such as strontium 89) within 3 months prior to Visit 2. Abnormal renal function as evidenced by A calculated creatinine clearance < 30 ml/minute. Creatinine clearance (CrCl) is calculated using the Cockcroft-Gault formula: CrCl= [140-age (years)] x weight (kg) {x 0.85 for female patients} [72 x serum creatinine (mg/dL)] Corrected (adjusted for serum albumin) serum calcium concentration < 8.0 mg/dl (2.00 mmol/L) or ≥ 12.0 mg/dl (3.00 mmol/L) Life expectancy < 6 months Patients with evidence in the six months prior to randomization of severe cardiovascular disease (defined as uncontrolled congestive heart failure), hypertension refractory to treatment, or symptomatic coronary artery disease uncontrolled by treatment Use of other investigational drugs (drugs not marketed for any indication) within 30 days prior to the date of randomization Current active dental problems including infection of the teeth or jawbone (maxilla or mandibular); dental or fixture trauma, or a current or prior diagnosis of osteonecrosis of the jaw (ONJ), of exposed bone in the mouth, or of slow healing after dental procedures. Recent (within 6 weeks) or planned dental or jaw surgery (e.g. extraction, implants) Other protocol-defined inclusion and exclusion criteria may apply.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Novartis Pharmaceuticals
    Organizational Affiliation
    Novartis Pharmaceuticals
    Official's Role
    Study Director

    12. IPD Sharing Statement

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    Effect of Zoledronic Acid in Patients With Prostate Cancer and Bone Metastasis

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