跳至主要内容
临床试验/JPRN-UMIN000007918
JPRN-UMIN000007918招募中未知

Safety and efficacy of lenalidomide, dexamethasone, and clarithromycin therapy in Japanese patients with multiple myeloma, a phase I/II study - lenalidomide, dexamethasone, and clarithromycin therapy in Japanese patients with multiple myeloma

ara Hospital Kinki University School Of Medicine0 个研究点目标入组 32 人开始时间: 2012年5月11日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
发起方
入组人数
32

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
20years-old 至 70years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • Cardiac infarction within 6 months Deep vein thrombosis or pulmonary embolism within 3 years Tuberculosis,herpes simplex keratitis, mycosis, or other active infections at baseline Uncontrollable diabetes mellitus, hypertension, peptic ulcer, or glaucoma Posterior capsule opacification Patients with mental illness Those who are considered as inappropriate to register by attending physicians Pregnant or breast feeding females Grade 2 or more peripheral neuropathy Any of following laboratory abnormalities Absolute neutrophil count < 1000 Platelet count< 75000 Creatinine clearance < 60 mL/ min Serum SGOT/AST or SGPT/ALT >3.0 x upper limit of normal Prior history of malignancies other than multiple myeloma unless the subject has been free of the disease for > 3 years Radiotherapy within 14 days Wound by recent organ surgery HIV-positive Known hypersensitivity to dexamethasone Known hypersensitivity to macrolides

研究者

发起方
ara Hospital Kinki University School Of Medicine

相似试验