PER-134-09已完成未知
A Phase IIb, Randomized, Double-Blind, Placebo- and Active-Controlled, Dose-Range-Finding Study to Evaluate the Effects of MK-5442 on Bone Mineral Density (BMD) in the Treatment of Osteoporosis in Postmenopausal Women Previously Treated With an Oral Bisphosphonate
MERCK & CO.INC.,0 个研究点目标入组 0 人开始时间: 2009年12月30日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 45 至 85(—)
- 性别
- Female
入选标准
- •Taking oral bisphosphonate treatment for osteoporosis for at least 3 of the past 4 years. At present, and for the past 12 months, treated with alendronate
- •Bone Mineral Density (BMD) T-score that is ≤ -1.5 at one or more of the following anatomic sites; lumbar spine, femoral neck, trochanter, and total hip, AND a BMD T-score at all of these sites that is ≥ -4.0, AND a history of at least one fragility fracture, OR, a BMD T-score that is ≤ -2.5 at one or more of the following anatomic sites; lumbar spine, femoral neck, trochanter, and total hip, AND a BMD T-score at all of these sites that is ≥ -4.0
- •Postmenopausal for at least 5 years
排除标准
- •Obesity (ie, weight greater than 250 pounds) that prohibits the use of dual-emission X-ray absorptiometry (DXA)
- •Received intravenous (IV) bisphosphonates, fluoride treatment at a dose >1 mg/day for more than 2 weeks, strontium, growth hormone, a cathepsin K (CTSK) inhibitor, or a receptor activator of nuclear factor kappa-B ligand (RANKL) inhibitor at any time in the past
- •Use of oral bisphosphonates other than alendronate in the last 12 months, parathyroid hormone (PTH) in the last 24 months, cyclosporin for more than 2 weeks in the last 6 months, heparin in the last 2 weeks, or anabolic steroids or glucocorticoids for more than 2 weeks in the past 6 months
- •Use of estrogen with or without progestin or a selective estrogen receptor modulator (SERM) in the last 6 months or calcitonin in the last 30 days
- •Has used pioglitazone hydrochloride or rosiglitazone hydrochloride in the last 6 months
- •Taking more than 10,000 International Units (IU) vitamin A daily or more than 5,000 IU vitamin D daily
- •Has had a total thyroidectomy
- •History of Paget´s disease
- •Has human immunodeficiency virus (HIV)
- •History of cancer in the last 5 years, except certain skin or cervical cancers
- •History of major upper gastrointestinal (GI) mucosal erosive disease
- •Unable to adhere to dosing instructions for alendronate in regard to fasting and positioning
- •Not ambulatory
研究者
相似试验
进行中(未招募)
不适用
Study in in Postmenopausal Women with OsteoporosisPostmenopausal OsteoporosisEUCTR2009-014729-18-CZMerck Sharp & dohme Corp. a Subsidiary of Merck & Co., Inc.320
进行中(未招募)
不适用
A Phase IIb, Randomized, Double-Blind, Placebo- and Active-Controlled, Dose-Range-Finding Study to Evaluate the Effects of MK-5442 on Bone Mineral Density (BMD) in the Treatment ofOsteoporosis in Postmenopausal Women Previously Treated with an Oral BisphosphonatePostmenopausal OsteoporosisEUCTR2009-014729-18-DKMerck & Co., Inc.480
进行中(未招募)
不适用
A Phase IIb, Randomized, Double-Blind, Placebo- and Active-Controlled, Dose-Range-Finding Study to Evaluate the Effects of MK-5442 on Bone Mineral Density (BMD) in the Treatment of Osteoporosis in Postmenopausal Women Previously Treated with an Oral BisphosphonateMedDRA version: 12.0Level: LLTClassification code 10031282Term: OsteoporosisPostmenopausal OsteoporosisEUCTR2009-014729-18-PLMerck & Co. Inc.520
进行中(未招募)
1 期
A Phase IIb, Randomized, Double-Blind, Placebo- and Active-Controlled, Dose-Range-Finding Study to Evaluate the Effects of MK-5442 on Bone Mineral Density (BMD) in the Treatment of Osteoporosis in Postmenopausal Women Previously Treated with an Oral BisphosphonateOsteoporosisEUCTR2009-014729-18-FRMerck & Co., Inc.670
已完成
2 期
MK5442 in the Treatment of Osteoporosis in Postmenopausal WomenPreviously Treated With an Oral Bisphosphonate (MK-5442-012 AM1)CTRI/2010/091/000258Merck Sharp and Dohme526
