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临床试验/EUCTR2019-003829-18-GB
EUCTR2019-003829-18-GB进行中(未招募)1 期

A Phase 3 Study of Danicopan (ALXN2040) as Add-on Therapy to a C5 Inhibitor (Eculizumab or Ravulizumab) in Patients with Paroxysmal Nocturnal Hemoglobinuria Who Have Clinically Evident Extravascular Hemolysis (EVH)

Alexion Pharmaceuticals Inc.0 个研究点目标入组 84 人开始时间: 2020年2月5日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
84

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

  • Diagnosis of PNH
  • Clinically Evident EVH defined by:
  • - Anemia (Hgb =9.5 gram/deciliter) with absolute reticulocyte count =120 x 10^9/liter.
  • - At least 1 packed red blood cell or whole blood transfusion within 6 months prior to the start of the study.
  • Receiving a C5 inhibitor for at least 6 months prior to Day 1
  • Platelet count =30,000/microliters (µL)
  • Absolute neutrophil counts =750/µL.
  • Documentation of/or willingness to receive vaccinations and prophylactic antibiotics as required.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range: 0
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 82
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 2

排除标准

  • History of a major organ transplant or hematopoietic stem cell transplantation (HSCT).
  • Participants with known aplastic anemia or other bone marrow failure that requires HSCT or other therapies including anti-thymocyte globulin and/or immunosuppressants.
  • Known or suspected complement deficiency.
  • Laboratory abnormalities at screening, including:
  • - Alkaline phosphatase >2 x upper limit of normal (ULN).
  • - Alanine aminotransferase >2 x ULN.
  • - Direct bilirubin >2 x ULN (unless due to EVH or documented Gilbert’s Syndrome.
  • Current evidence of biliary cholestasis.
  • Estimated glomerular filtration rate <30 milliliters/minute/1.73 meter squared and/or are on dialysis.

研究者

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