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临床试验/EUCTR2006-003854-33-IT
EUCTR2006-003854-33-IT进行中(未招募)不适用

A multi-centre, randomised studyof Zoledronic Acid versus Observationin Patients with Asymptomatic Myeloma - ND

AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI0 个研究点开始时间: 2007年6月27日最近更新:
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试验速览

阶段
不适用
状态
进行中(未招募)
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Understanding and voluntary signing of informed consent form (ICF)
  • Age 18 years at the time of signing ICF
  • Newly diagnosed asymptomatic MM
  • Asymptomatic MM, previously followed-up, with stable serum or urine M component (no
  • 50% increase in serum or urine M component during the last 24 months)
  • Measurable M component in serum (
  • 1.0 g/L for IgG, 0.5g/L for IgA or IgM) or urine (
  • 0.2g/ 24h)
  • Bone marrow plasmacytosis > 10%
  • Absence of signs or symptoms of end organ damage attributable to neoplastic plasma cell
  • proliferation
  • No evidence of bone involvement at standard X-ray survey (osteolytic lesions, pathological
  • fractures) or MRI (structural damage or tumor masses; focal or diffuse signal alterations allow
  • Performance status ECOG 0-3
  • Bilirubin serum level < 2.5mg/dl
  • SGOT/SGPT < 2N
  • Ability to comply with trial requirements
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Symptomatic MM
  • Non secretory MM
  • Extramedullary plasmacytoma
  • Previous bisphosphonate therapy ( a three-month wash-out required in caso of treatment with
  • oral bisphosphonates for benign osteoporosis)
  • Hypersensitivity to bisphosphonates
  • Previous therapy for MM (either cytotoxic or Thalidomide/Thalidomide analogues/Bortezomib) Corrected serum calcium < 8mg/dl Hypercalcemia (1mg/dl > normal)
  • Calculated creatinine clearance < 30 ml/min or creatinine 1mg/dl > normal
  • Pregnancy or childbearing potential without any contraception method adopted
  • Prevoius history of malignancy other than MM, unless the subject has been free of the disease
  • for 5 years, except in situ carcinoma of the cervix or skin
  • Previous cancer metastatic to the bone
  • Bone-related disorder (e.g. Paget disease)
  • Amyloidosis
  • Any psychiatric illness impairing the ability to comply with trial requirements
  • 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 (see appendix
  • for details).
  • Recent (within 6 weeks) or planned dental or jaw surgery (e.g. extraction, implants) (see
  • appendix for details)

研究者

发起方
AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI

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