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临床试验/CTIS2024-516438-36-00
CTIS2024-516438-36-00进行中(未招募)1 期

A phase II, open-label, single arm study to evaluate the efficacy of Luspatercept in Erythropoiesis-stimulatingagent naive lower-risk MDS patients with or without ring sideroblasts who do not require RBC transfusions (LENNON) - LENNO

niversitaet Leipzig0 个研究点目标入组 30 人开始时间: 2024年8月5日最近更新:

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
30

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

年龄范围
18 至 65+(—)
性别
All

入选标准

  • Diagnosis of MDS according to WHO classification, Very low-, low-, or intermediate-risk disease with up to 3.5 score points according to revised International Prognostic Scoring System (IPSS-R) classification, Non-transfusion dependence (NTD) according to IWG 2018, Symptomatic anemia: mean baseline Hb < 10 g/d

排除标准

  • Secondary MDS, Known clinically significant anemia due to iron, vitamin B12, or folate deficiencies, or autoimmune or hereditary hemolytic anemia, or gastrointestinal bleeding, Prior allogeneic or autologous stem cell transplant, ECOG > 2, Prior ESA treatment

研究者

发起方
niversitaet Leipzig

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