NCT07653581尚未招募3 期
rhTPO + CsA Versus CsA Alone in the Treatment of Lower-risk MDS With Thrombocytopenia: a Single-center Randomized Controlled Trial
适应症
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 入组人数
- 78
研究概览
简要总结
This study aims to compare the efficacy and safety of recombinant human thrombopoietin (rhTPO) + cyclosporine (CsA) and CsA monotherapy in the treatment of lower-risk myelodysplastic neoplasms with thrombocytopenia.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age ≥ 18 years old;
- •Confirmed diagnosis of lower-risk MDS;
- •Platelet ≤ 30×109/L, or < 50×109/L and accompanied by bleeding events;
- •Baseline liver and kidney functions <2 ULN;
- •Signed the informed consent form;
排除标准
- •History of leukemia or stem cell transplantation, treatment-related MDS or malignant tumors;
- •With splenomegaly or myelofibrosis;
- •Infections or bleeding that cannot be controlled by standard treatment;
- •Any concurrent malignant tumors within the past 5 years, or basal cell carcinoma of the skin at the local site;
- •History of thromboembolic events, heart attack or stroke and current use of anticoagulants;
- •Previously received cyclosporine (CsA) or ATG within 6 months;
- •Previously used IL-11, rhTPO or TPO-RA;
- •Pregnant or lactating women;
- •Participated in other clinical trials within 3 months.
研究者
Bing Han
Professor
Peking Union Medical College Hospital
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