跳至主要内容
临床试验/EUCTR2017-000586-72-PT
EUCTR2017-000586-72-PT进行中(未招募)1 期

KRd consolidation in myeloma patients with a positive PET-CT after standard first line treatment. A phase II study - CONPET

Oslo University Hospital0 个研究点目标入组 50 人开始时间: 2020年10月30日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1. Prior confirmed diagnosis of multiple myeloma (2014).
  • 2. Received standard first line treatment with at least partial response. Standard first line treatment is defined as VRD, VTD or VCD followed by ASCT, with or without lenalidomide maintenance
  • 3. Carfilzomib naïve
  • 4. Eastern Cooperative Oncology Group (ECOG) performance status 0-2.
  • 5. Absolute neutrophil count (ANC) = 0,5 x 109/L and platelet count >35 x 109/L.
  • 6. At least very good partial remission (VGPR) from first line treatment
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 25
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 25

排除标准

  • 1. Change of first line treatment because of stabile or progressive disease.
  • 2. Major surgery within 28 days before enrollment.
  • 3. Radiotherapy within 14 days before enrollment.
  • 4. Glucocorticoid therapy within the 14 days prior to inclusion that exceeds a cumulative dose of 160 mg dexamethasone or 1000 mg prednisone.
  • 5. Patients who started treatment more than 12 month before screening
  • 6. Central nervous system involvement.
  • 7. Uncontrolled heart disease, including congestive heart failure (NYHA III-IV), uncontrolled angina pectoris, uncontrolled conduction abnormalities, acute diffuse infiltrative pulmonary disease, pericardial disease or myocardial infarction within 6 months prior to enrollment
  • 8. Uncontrolled hypertension or uncontrolled diabetes despite medication
  • 9. Active hepatitis B or C infection or known human immunodeficiency virus (HIV) positivity.
  • 10. Another active malignancy. Patients with non-melanoma skin cancer or carcinoma in situ of any type are not excluded if they have undergone complete resection.
  • 11. Primary plasma cell leukemia, systemic AL amyloidosis, Waldenströms macroglobulinemia, POEMS syndrome
  • 12. Not expected to tolerate full dose KRd

研究者

发起方
Oslo University Hospital

相似试验