Prostate Cancer Patients With Bone Metastasis
Conditions
Keywords
Prostate cancer, Bone metastasis, Skeletal related event
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.
Interventions
DRUGZoledronic acid
Sponsors
Novartis Pharmaceuticals
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Rate of skeletal complications | 3 months |
Secondary
| Measure | Time frame |
|---|---|
| Time to first skeletal complication | 3 months |
| Bone pain | 3 months |
| Patients´ satisfaction with treatment | 3 months |
| Bone turnover parameters | 3 months |
Outcome results
None listed