EUCTR2012-002471-34-DK进行中（未招募）不适用
A Phase 3, Multicenter, Randomized, Double-Blind Study to Compare the Efficacy and Safety of Oral Azacitidine Plus Best Supportive Care Versus Placebo Plus Best Supportive Care in Subjects With Red Blood Cell Transfusion-Dependent Anemia And Thrombocytopenia due to IPSS Lower-Risk Myelodysplastic Syndromes - QUAZAR lower-risk MDS
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 入组人数
- 386
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. Age = 18 years at the time of signing the informed consent document
- •2. Have a documented diagnosis of MDS according to WHO 2008 classification
- •3. Be RBC transfusion-dependent as defined by:
- •Average transfusion requirement of = 2 units** per 28 days of RBCs confirmed for a minimum of 84 days immediately preceding randomization (please note that the period covering the transfusion history overlaps with the screening phase)
- •o Hemoglobin levels at the time of or within 7 days prior to administration of an RBC transfusion must have been = 9.0 g/dL in order for the transfusion to be counted towards RBC transfusion-dependent status. Red blood cell transfusions administered when Hgb levels were > 9.0 g/dL and/or RBC transfusions administered for elective surgery will not qualify as a required transfusion for the purpose of providing evidence of RBC transfusion-dependent status
- •- No consecutive 42 days that are RBC-transfusion-free during the 84 days immediately preceding randomization
- •4. Have thrombocytopenia as defined by two platelet counts that are = 75 x 109/L and = 21 days apart (analyzed by the central laboratory). The second confirmatory platelet count must be obtained = 14 days prior to randomization
- •o If additional platelet counts were obtained during the interim period, these must also have been = 75 x 109/L. Platelet counts > 75 x 109/L within the interim period are acceptable only if directly associated with a platelet transfusion administered within 7 days prior to the date of the platelet count
- •5. Have an ECOG performance status of 0, 1, or 2
- •6. Females of childbearing potential (FCBP)†† may participate, providing they meet the following conditions:
- •o Agree to use at least two effective contraceptive methods (oral, injectable, or implantable hormonal contraceptive; tubal ligation; intra-uterine device; barrier contraceptive with spermicide; or vasectomized partner) throughout the study, and for 3 months following the last dose of study drug; and
- •o Have a negative serum pregnancy test at screening ; and
- •o Have a negative serum or urine pregnancy test (investigator’s discretion; sensitivity of at least 25 mIU/mL) within 72 hours prior to starting study therapy in the treatment phase (note that the screening serum pregnancy test can be used as the test prior to starting study therapy in the treatment phase if it is performed within the 72-hour timeframe)
- •7. Male subjects with a female partner of childbearing potential must agree to the use of at least two physician-approved contraceptive methods throughout the course of the study and should avoid fathering a child during the course of the study and for 3 months following the last dose of study drug
- •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 86
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 300
排除标准
- •1. IPSS higher-risk (INT-2 or High risk) MDS
- •2. Secondary MDS, ie MDS that is known to have arisen as the result of chemical injury or treatment with chemotherapy and/or radiation for other diseases, unless subject received last dose from prior antineoplastic therapy = 24 weeks prior to randomization
- •3. Hypoplastic MDS or other subtype with eligibility for treatment with immunotherapy based on investigator’s judgment, unless subject received last dose from prior Chemo~ or Immunotherapy = 24 weeks prior to randomization
- •4. CMML, atypical chronic myeloid leukemia (CML) and unclassifiable myeloproliferative disease (MPD)
- •5. Prior treatment with any of the following:
- •Azacitidine (any formulation), decitabine or other hypomethylating agent
- •Lenalidomide, unless the subject received the last dose = 24 weeks prior to randomization
- •6. Prior allogeneic or autologous stem cell transplant
- •7. History of inflammatory bowel disease (eg, Crohn’s disease, ulcerative colitis), celiac disease (ie, sprue), prior gastrectomy or upper bowel removal, or any other gastrointestinal disorder or defect that would interfere with the absorption, distribution, metabolism or excretion of the study drug and/or predispose the subject to an increased risk of gastrointestinal toxicity
- •8. Thrombocytopenia secondary to other possible causes, including medication(s), congenital disorder(s), immune disorder(s) (eg, idiopathic thrombocytopenic purpura [ITP]), or microvascular disorder(s) (eg, disseminated intravascular coagulation, hemolytic uremic syndrome, thrombotic thrombocytopenic purpura)
- •9. Use of any of the following within 28 days prior to randomization:
- •cytotoxic, chemotherapeutic, targeted or investigational agents/therapies
- •thrombopoiesis-stimulating agents (TSAs; eg, Romiplostim, Eltrombopag, Interleukin-11)
- •ESAs and other RBC hematopoietic growth factors (eg, Interleukin-3)
- •hydroxyurea
- •10. Ongoing medically significant adverse events from previous treatment, regardless of the
- •time period
- •11. Concurrent use of any of the following:
- •iron-chelating agents, except for subjects on a stable or decreasing dose for at least 8 weeks (56 days) prior to randomization
- •corticosteroid, except for subjects on a stable or decreasing dose for = 1 week prior to randomization for medical conditions other than MDS
- •12. Prior history of malignancies, other than MDS, unless the subject has been free of the disease for = 3 years. However, subjects with the following history/concurrent conditions are allowed:
- •Basal or squamous cell carcinoma of the skin
- •Carcinoma in situ of the cervix
- •Carcinoma in situ of the breast
- •Incidental histologic finding of prostate cancer (T1a or T1b using the tumor, nodes, metastasis [TNM] clinical staging system)
- •13. Significant active cardiac disease within the previous 6 months, including:
- •New York Heart Association (NYHA) class IV congestive heart failure;
- •Unstable angina or angina requiring surgical or medical intervention; and/or
- •Myocardial infarction
- •14. Uncontrolled systemic fungal, bacterial, or viral infection (defined as ongoing signs/symptoms related to the infection without improvement despite appropriate antibiotics, antiviral therapy, and/or other treatment)
- •15. Known Human Immunodeficiency Virus (HIV) or Hepatitis C (HCV) infection, or evidence of active Hepatitis B Virus (HBV) infection
- •16. Abnormal coagulation parameters (PT > 15 seconds, PTT > 40 seconds, and/or INR > 1.5)
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