EUCTR2006-006577-25-SE进行中（未招募）不适用
A prospective randomized study comparing rapamune and tacrolimus vs. cyclosporine and methotrexate as immune prophylaxis in allogeneic hematopoietic stem cell transplantation, using HLA-A, -B, -DRB1 identical related or unrelated donors. A Nordic multicenter study. - Rapa + FK in stem cell transplantation
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 入组人数
- 200
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
- •Patients who receives bone marrow or peripheral blood stem cells from an HLA-identical sibling donor or an unrelated genomically matched HLA-A, -B and -DRb1 identical donor. No more than one alleles mismatch is allowed. The study includes children and adults undergoing full myeloablative or non-myeloablative conditioning, according to established protocols. Chronic myeloid leukemia (CML) in 1st or 2nd chronic phase, acute myeloid leukemia (AML) in complete remission, acute lymphoblastic leukemia (ALL) in complete remission, myelodysplastic syndrome, chronic lymphocytic leukemia, lymphoma, non-malignant disorders, severe aplastic anemia, hemoglobinopathies and metabolic disorders. More or less all diagnoses where there is an indication for hematopoietic stem cell transplantation with a related or unrelated HLA-identical donor may be included in the study. The inclusion of various cohorts of patients is at the discretion of each participating center – i.e., some centers may only want to include unrelated donors, other may want to include related and unrelated donors, and other centers may be more specific with regard to the various diagnoses
- •Are the trial subjects under 18? yes
- •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
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Recipients of major HLA-mismatched grafts. Patients who are addicted to drugs or alcohol. Patients who receive other stem cell source than bone marrow or peripheral stem cells, for instance cord blood transplants. Patients with relapse or blast crisis of their malignant disease. Prior allogeneic transplant using any hematopoietic stem cell source Seropositive for the human immunodeficiency virus (HIV) Uncontrolled bacterial, viral, or fungal infection (progression of clinical symptoms) Pregnant (positive serum human chorionic gonadotropin [ß-HCG] test) or breastfeeding within 4 weeks of study entry Kidney function: serum creatinine outside the normal range for age, or measured creatinine clearance less than 40 mL/min/1.72m² within 4 weeks of study entry and proteinuria >0.3 g/day Liver function: most recent direct bilirubin, ALT, or AST greater than two times the upper limit of normal within 4 weeks of study entry Lung disease: in adults, FVC or FEV1 less than 60% of predicted value (corrected for hemoglobin); in children, overt hypoxemia, as measured by an oxygen saturation of less than 92% within 4 weeks of study entry Cardiac ejection fraction of less than 45% in adults and children, or less than 26% shortening fraction in children within 4 weeks of study entry Cholesterol level greater than 300 mg/dL or triglyceride level greater than 300 mg/dL while being treated, or not on appropriate lipid-lowering therapy within 4 weeks of study entry Karnofsky score <70% Prior history of allergy to sirolimus Requires voriconazole at time of study entry Currently receiving another investigational drug unless cleared by the principal investigator and sponsor
研究者
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A prospective randomized study comparing rapamune and tacrolimus vs. cyclosporine and methotrexate as immune prophylaxis in allogeneic hematopoietic stem cell transplantation, using HLA-A, -B, DRß1 identical related or unrelated donors. A Nordic multicenter studyPatients treated with allogeneic haematopoietic stem cell transplantationEUCTR2006-006577-25-FIordic Bone Marrow Transplant Group (NBMT)200
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