Clinical trial · Interventional
Effect of Zoledronic Acid in Patients With Prostate Cancer and Bone Metastasis
NCT00237159CI-TRIAL-00004587completedPhase 4ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Prostate Cancer Patients With Bone Metastasis | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Zoledronic acid | Drug | Zoledronic Acid | ALIAS |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- ZOL446
- interventionNames
- Drug: Zoledronic acid
Primary outcomes (1)
- measure
- Rate of skeletal complications
- timeFrame
- 3 months
Secondary outcomes (4)
- measure
- Time to first skeletal complication
- timeFrame
- 3 months
- measure
- Bone pain
- timeFrame
- 3 months
Eligibility
Eligibility (as posted)
- Sex
- Male
- Minimum age
- 18 Years
Show eligibility criteria text
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.References
Publications (0)
Data not yet available
No reference posted for this study.