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临床试验/NCT00447915
NCT00447915已完成3 期

Phase II/III Clinical Study of R484iv (Ibandronic Acid) for Primary Osteoporosis - Comparative Study With Sodium Risedronate Hydrate(RIS) With Vertebral Fracture as an Index -

Chugai Pharmaceutical4 个研究点 分布在 1 个国家目标入组 1,265 人开始时间: 2007年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
1,265
试验地点
4
主要终点
Incidence of vertebral fracture

研究概览

简要总结

To evaluate the efficacy and safety of R484iv by intravenous intermittent administration to patients with primary osteoporosis in comparison with sodium risedronate hydrate (RIS) by oral administration every day. To evaluate also the dose response of R484iv.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
60 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with fragile bone fracture
  • Patients in whom either of study site analysis value of bone density of lumbar spine, proximal part of femur or neck of femur is less than 80% of young adult mean (YAM).
  • Patients with 1 - 5 bone fractures in 4th thoracic spine (Th4) - 4th lumbar spine (L4)
  • Ambulatory

排除标准

  • Patients with disease lowering bone volume secondarily (secondary osteoporosis)
  • Patients receiving at least one time of of oral bisphosphonate preparations within 6 months before the start of administration of the study drug
  • Patient with disorder delaying the passage of food through esophagus

研究组 & 干预措施

1

Experimental

干预措施: ibandronic acid 0.5mg (Drug)

1

Experimental

干预措施: RIS placebo (Drug)

1

Experimental

干预措施: Calcium and Vitamine D3 (Dietary Supplement)

2

Experimental

干预措施: RIS placebo (Drug)

2

Experimental

干预措施: 1.0mg ibandronic acid (Drug)

2

Experimental

干预措施: Calcium and Vitamine D3 (Dietary Supplement)

3

Active Comparator

干预措施: ibandronic acid placebo (Drug)

3

Active Comparator

干预措施: 2.5mg RIS (Drug)

3

Active Comparator

干预措施: Calcium and Vitamine D3 (Dietary Supplement)

结局指标

主要结局

Incidence of vertebral fracture

时间窗: 36 months

次要结局

  • Change of bone density of lumbar spine and proximal part of femur from baseline(36 months)
  • Change of bone absorption marker from baseline(36 months)
  • Change of bone formation marker from baseline(36 months)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (4)

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