Therapy With Zoledronic Acid in Patients With Multiple Myeloma Stage I
Multiple Myeloma Stage I
About this trial
This is an interventional treatment trial for Multiple Myeloma Stage I focused on measuring Multiple Myeloma, Stage I, Zoledronic acid, Progression
Eligibility Criteria
Inclusion Criteria Evidence of myeloma according to the criteria of the British Columbia Cancer Agency (for the diagnosis, 2 of the 3 criteria must be met): Evidence of paraprotein in the serum or urine Bone marrow infiltration with plasma cells which represent more than 10% of the nucleated cells Radiologically, at least one osteolytic lesion Asymptomatic patients with Stage I (Durie and Salmon) multiple myeloma Exclusion criteria: Patients with more than one osteolytic lesion on conventional skeletal radiography Previous treatment with bisphosphonates bilirubin > 2.5 mg/dl 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)/[72xserumcreatinine(mg/dL)] X {0.85 for female patients} Patients with other malignant diseases or severe concomitant diseases Potentially fertile patients who are not using a reliable and appropriate method of contraception Pregnancy or breast-feeding Participation in another clinical study with an investigational drug within 12 weeks of study entry 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
- Novartis Investigative Site
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Zoledronic acid (ZOL446)
Control
Participants received intravenous infusion of Zoledronic acid every 4 weeks for 48 weeks, and calcium and Vitamin D daily.
No treatment with study medication.