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临床试验/PER-036-23
PER-036-23尚未招募3 期

A RANDOMIZED, OPEN-LABEL, C5 INHIBITOR-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF POZELIMAB AND CEMDISIRAN COMBINATION THERAPY IN PATIENTS WITH PAROXYSMAL NOCTURNAL HEMOGLOBINURIA WHO ARE COMPLEMENT INHIBITOR TREATMENT-NAIVE OR HAVE NOT RECENTLY RECEIVED COMPLEMENT INHIBITOR THERAPY

REGENERON PHARMACEUTICALS, INC.0 个研究点目标入组 0 人开始时间: 2024年5月24日最近更新:
适应症

试验速览

阶段
3 期
状态
尚未招募

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

性别
All

入选标准

  • 1. Diagnosis of PNH confirmed by high-sensitivity flow cytometry testing with PNH granulocytes described in the protocol
  • 2. Active disease, as defined by the presence of 1 or more PNH-related signs or symptoms described in the protocol
  • 3. LDH level =2 × upper limit of normal (ULN) at the screening visit

排除标准

  • 2. Receipt of an organ transplant, history of bone marrow transplantation or other hematologic transplant
  • 3. Body weight <40 kilograms at screening visit
  • 4. Planned use of any complement inhibitor therapy other than study drugs during the treatment period
  • 1. Prior treatment with eculizumab within 3 months prior to screening, ravulizumab within 6 months prior to screening, or other complement inhibitors within 5 half-lives of the respective agent prior to screening
  • 5. Not meeting meningococcal vaccination requirements for ravulizumab (Cohort A) or eculizumab (Cohort B) according to the current local prescribing information (where available) and at a minimum documentation of meningococcal vaccination within 5 years prior to screening visit
  • 6. Any contraindication for receiving Neisseria meningitidis vaccination
  • 7. Unable to take antibiotics for meningococcal prophylaxis (if required by local ravulizumab [Cohort A] or eculizumab [Cohort B] prescribing information, where available, or national guidelines/local practice or if necessary, when vaccination is less than 2 weeks from study treatment initiation)
  • 8. Any active, ongoing infection or a recent infection requiring ongoing systemic treatment with antibiotics, antivirals, or antifungals within 2 weeks of screening or during the screening period
  • 9. Documented history of active, uncontrolled, ongoing systemic autoimmune diseases

研究者

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