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临床试验/NCT06979076
NCT06979076尚未招募1 期

A Phase Ib Study of the Selective PKC-β Inhibitor MS-553 in Patients With Refractory or Relapsed Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma

MingSight Pharmaceuticals, Inc0 个研究点目标入组 12 人开始时间: 2026年7月1日最近更新:
干预措施
相关药物

试验速览

阶段
1 期
状态
尚未招募
发起方
入组人数
12
主要终点
The occurrence of AEs and SAEs, with abnormal laboratory tests results, abnormal physical examination findings, abnormal vital signs, and abnormal ECG readings

研究概览

简要总结

A Phase Ib Study of the Selective PKC-β Inhibitor MS-553 in Patients with Refractory or Relapsed Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma

研究设计

研究类型
Interventional
分配方式
Non 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

入选标准

  • Age 18 years or older.
  • Diagnosis of CLL or SLL:
  • History of histologically documented CLL or SLL that meets iwCLL diagnostic criteria according to the 2018 guidelines, and
  • Indication for treatment as defined by the 2018 iwCLL guidelines, or the need for disease reduction prior to allogeneic transplantation.-

排除标准

  • Current transformation of CLL/SLL non-Hodgkin lymphoma or Hodgkin lymphoma.
  • Active and uncontrolled autoimmune cytopenia(s).

研究组 & 干预措施

MS-553, dose schedule 2 (DS2)

Experimental

干预措施: MS-553, DS2 (Drug)

MS-553, dose schedule 1 (DS1)

Experimental

干预措施: MS-553, DS1 (Drug)

结局指标

主要结局

The occurrence of AEs and SAEs, with abnormal laboratory tests results, abnormal physical examination findings, abnormal vital signs, and abnormal ECG readings

时间窗: Through study completion, an average of 2 years

次要结局

未报告次要终点

研究者

发起方
MingSight Pharmaceuticals, Inc
申办方类型
Industry
责任方
Sponsor

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