Overview

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

Status:
Completed
Trial end date:
1969-12-31
Target enrollment:
0
Participant gender:
Male
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.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Novartis Pharmaceuticals
Treatments:
Diphosphonates
Zoledronic Acid
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.