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临床试验/NCT06633536
NCT06633536进行中(未招募)不适用

Real-life Treatment Outcomes of Ravulizumab in Polish Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH). Prospective and Retrospective, Multicenter, Non-interventional Study.

AstraZeneca11 个研究点 分布在 1 个国家目标入组 64 人开始时间: 2025年2月6日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
AstraZeneca
入组人数
64
试验地点
11
主要终点
Change in LDH levels from index date (first dose of ravulizumab) at every 6 month

研究概览

简要总结

The PNH-RECORD study, a Polish multicenter observational (non-interventional), open-label, retrospective with prospective follow-up.

详细描述

PNH-RECORD study aims to aims to collect data on the patients' characteristics and clinical outcomes of ravulizumab administered in the scope of routine clinical practice in PNH.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

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

  • Adult (aged ≥18) patients with PNH receiving ravulizumab treatment in the frames of NDP in Poland.
  • Patients willing to participate in the study and signed ICF.

排除标准

  • Those who participated in ravulizumab clinical trial in the past, and/or those who participated/plans to participate in clinical trial on/after the date of first ravulizumab infusion through NDP.
  • Cognitive incapacity, unwillingness or language barriers precluding adequate understanding or cooperation.

研究组 & 干预措施

Ravulizumab group

Open-label

干预措施: Ravulizumab (Drug)

结局指标

主要结局

Change in LDH levels from index date (first dose of ravulizumab) at every 6 month

时间窗: up to 36 months

Proportion of patients achieving or remaining at LDH<1.5 ULN at every 6 month

时间窗: up to 36 months

次要结局

  • Proportion of transfusion-free patients from index date at every 6 month(up to 36 months)
  • Number of blood units used per patient-year(up to 36 months)
  • To present clinical characteristics(Baseline)
  • To present patients characteristics(Baseline)

研究者

发起方
AstraZeneca
申办方类型
Industry
责任方
Sponsor

研究点 (11)

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