An Open Label Academic Phase 2 Study of SDMB in Subjects in Thailand With Beta Thalassemia Intermedia
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 10
- 试验地点
- 1
- 主要终点
- The number of participants in which an increase in total hemoglobin of at least 1.5 g/dl above average baseline occurs with study drug treatment.
研究概览
简要总结
Beta thalassemia intermedia is an inherited blood disease caused by molecular mutations which reduce the beta globin protein chain of adult hemoglobin A, the protein in red blood cells which carries oxygen throughout the body. Beta thalassemias cause progressively severe anemia, widespread organ damage, and often require blood transfusions. There is no FDA approved therapeutic to treat the underlying cause of beta thalassemia. Fetal hemoglobin is another type of endogenous hemoglobin which can replace the reduced beta globin protein, reduce the anemia, and even abolish transfusion requirements. This type of hemoglobin is normally suppressed in infancy.
Sodium 2,2 dimethylbutyrate (ST20, or HQK-1001) is a small molecule which stimulates production of fetal hemoglobin in nonhuman primates and in human patients in Phase I/II trials.
This is a Phase 2 open-label trial to evaluate the ability of this oral therapeutic to reduce anemia in patients with beta thalassemia intermedia, when administered once daily for 26 weeks. All participants will receive the study drug.
详细描述
This trial will:
- Determine the proportion of patients in which treatment with the study drug results in an increase in total hemoglobin by 1.5 g/dl above baseline levels when administered for 26 weeks in Thai patients with beta thalassemia intermedia, including Hemoglobin E beta thalassemia.
- Determine the number and proportion of participants in whom treatment with the study drug results in an increase in fetal hemoglobin.
- Determine the number of participants who have adverse events.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 55 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Diagnosis of Beta Thalassemia Intermedia
- •Splenectomized
- •Average of two Hgb levels between 6.0 and 9.0 g/dl
排除标准
- •Red blood cell transfusion within 3 months of study drug initiation
- •Enlarged spleen
- •Use of hydroxyurea within 6 months
- •QT Segment corrected (QTc)> 450 msec (men) or 470 msec (women) on screening ECG
- •Use of iron chelating agents within 7 days of first dose
- •Alanine Transaminase(ALT)> 4 times the upper limit of normal
- •Use of erythropoiesis stimulating agents (ESAs) within 90 days of first dose
- •serum creatinine > 1.5 mg/dL
研究组 & 干预措施
Treatment
Study drug treatment
干预措施: sodium 2,2 dimethylbutyrate (Drug)
结局指标
主要结局
The number of participants in which an increase in total hemoglobin of at least 1.5 g/dl above average baseline occurs with study drug treatment.
时间窗: Within 30 weeks, including 26 weeks of dosing with the study drug
Baseline hemoglobin levels will be determined by averaging 2 values prior to administration of the study drug. The number of participants in which an increase in total hemoglobin of at least 1.5 g/dL above baseline occurs will be determined.
次要结局
- The proportion of participants in which an increase in fetal hemoglobin occurs above the subjects' averaged baseline levels.(Within 30 weeks, including 26 weeks of study drug administration)
研究者
Susan P. Perrine
Sponsor Investigator
Boston University