NL-OMON30155已完成3 期
A Randomized, Double-Blind, Multicenter Study of Denosumab Compared With Zoledronic Acid (Zometa) in the Treatment of Bone Metastases in Subjects with Advanced Cancer (Excluding Breast and Prostate Cancer) or Multiple Myeloma - Denosumab 20050244
Amgen Inc.0 个研究点目标入组 18 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 18
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
- 18 至 99(—)
入选标准
- •- adult with histologically or cytologically confirmed advanced cancers including solid tumors, multiple myeloma, and lymphoma ;- current or prior radiographic (ie, x-ray, computer tomography [CT], or magnetic resonance imaging [MRI]) evidence of at least 1 bone metastasis (or lytic bone lesion from multiple myeloma);- Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2;- adequate organ function as defined by the following criteria:
- •* serum aspartate aminotransferase (AST) * 5 x upper limit of normal (ULN)
- •* serum alanine aminotransferase (ALT) * 5 x ULN
- •* serum total bilirubin * 2 x ULN
- •* creatinine clearance (Cockroft-Gault) * 30 mL/min
- •* albumin-adjusted serum calcium * 2.0 mmol/L (8.0 mg/dL) and * 2.9 mmol/L (11.5 mg/dL). ;- Before any study-specific procedure is performed, the appropriate written informed consent must be obtained.
排除标准
- •- diagnosis of breast or prostate cancer.
- •- current or prior IV bisphosphonate administration.
- •- current or prior oral bisphosphonate for the treatment of bone metastasis / osteolytic lesion.
- •- planned radiation therapy or surgery to bone.
- •- prior administration of denosumab.
- •- known brain metastases.
- •- life expectancy less than 6 months.
- •- prior history or current evidence of osteonecrosis/osteomyelitis of the jaw.
- •- active dental or jaw condition which requires oral surgery.
- •- non-healed dental/oral surgery.
- •- planned invasive dental procedure over the course of the study.
- •- evidence of any of the following conditions per subject self report or medical chart review:
- •* any other prior malignancy (other than basal cell carcinoma, or in situ cervical cancer) with active disease within 3 years before randomization
- •* known infection with human immunodeficiency virus
- •* active infection with Hepatitis B or Hepatitis C virus
- •- any organic or psychiatric disorder that, in the opinion of the investigator, might prevent the subject from completing the study or interfere with the interpretation of the study results.
- •- thirty days or less since receiving an investigational product or device (ie, does not have marketing authorization; thalidomide use is allowed) in another clinical trial.
- •- pregnant or breast-feeding women.
- •- subject with reproductive potential who will not agree to use effective contraception (as defined by the principal investigator or designee).
- •- known sensitivity to any of the products to be administered during the study (eg, zoledronic acid, mammalian derived products, calcium or vitamin D).
研究者
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