跳至主要内容
临床试验/CTRI/2015/06/005944
CTRI/2015/06/005944进行中(未招募)3 期

enalidomide plus low dose Dexamethasone versus Thalidmide plus low dose Dexamethasone for Multiple Myeloma: A Randomized Phase III study

Dr Reddys Laboratories Ltd0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
进行中(未招募)

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

入选标准

  • a) Age 18 to 70 years
  • b) Adequate hemogram, liver, heart and kidney function
  • c) Performance status 0 to 2 (ECOG)
  • d) Two negative pregnancy tests (one before and the second 4 weeks after starting Thalidomide or Lenalidomide)
  • e) Willingness to participate in the study

排除标准

  • Hypersensitivity reaction to Thalidomide or Lenalidomide in the past
  • b) Pre-existing peripheral neuropathy more than grade 2
  • c) Uncontrolled diabetes mellitus
  • d) Renal failure
  • e) Significant ischemic cardiac disease eg LBBB
  • f) Uncontrolled psychiatric (depressive) disorder

研究者

相似试验

进行中(未招募)
不适用
enalidomide and dexamethasone (Ld) versus Clarithromycin / Lenalidomide [Revlimid®] / Dexamethasone (BiRd) as initial therapy in Multiple Myeloma.Multiple Myeloma
EUCTR2015-001183-19-ESFundación PETHEMA306
进行中(未招募)
1 期
The combination of Lenalidomide and Dexamethasone with or without intensification by high-dose Melphalan in the treatment of multiple myelomaprimary treatment of multiple myeloma patients of age 60 till 75 yearsMedDRA version: 21.0Level: LLTClassification code 10028228Term: Multiple myelomaSystem Organ Class: 100000004864
EUCTR2008-004083-39-DEGMIHO Gesellschaft für Medizinische Innovation – Hämatologie und Onkologie mbH348
招募中
不适用
ow dose of lenalidomide and dexamethasone therapy for eldery multiple myelomaRefractory or relapsed symptomatic multiple myeloma
JPRN-UMIN000008918ishiwaki municipal hospital26
进行中(未招募)
不适用
enalidomide and Dexamethasone for treatment of patients with acute myeloma (light chain)-induced renal failureThere are two patient groups to be included into the study:1) Patients with previously unknown MM and acute light chain induced renal failure 2) Patients with previously diagnosed MM, normal or near normal renal function (GFR minimum 60ml/min and serum creatinine =1.2mg/dl) within the previous 6 weeks before onset of acute light chain induced deterioration of renal function to GFR <50ml/min and serum creatinine not less than 2mg/dL.
EUCTR2008-006497-15-ATWilhelminen Krebsforschung GmbH50
进行中(未招募)
1 期
enalidomide and Dexamethasone for treatment of patients with acute myeloma (light chain)-induced renal failure - LDThere are two patient groups to be included into the study:1) Patients with previously unknown MM and acute light chain induced renal failure 2) Patients with previously diagnosed MM, normal or near normal renal function (GFR minimum 60ml/min and serum creatinine =1.2mg/dl) within the previous 6 weeks before onset of acute light chain induced deterioration of renal function to GFR <50ml/min and serum creatinine not less than 2mg/dL.
EUCTR2008-006497-15-SKWilhelminen Krebsforschung GmbH50