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OpenTrials
Completed

NCT Number: NCT00237159

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

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.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Zoledronic acid

Drug

Other names: ZOL446

Primary outcomes

  1. Rate of skeletal complications

    Time frame: 3 months

Secondary outcomes

  1. Time to first skeletal complication

    Time frame: 3 months

  2. Bone pain

    Time frame: 3 months

  3. Patients´ satisfaction with treatment

    Time frame: 3 months

  4. Bone turnover parameters

    Time frame: 3 months

Sponsors and collaborators

Lead sponsor

Novartis Pharmaceuticals

Industry

Registry information

Important dates

Study start
2002
Primary completion
2005
First posted
Oct 12, 2005
Registry last updated
Mar 23, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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