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临床试验/NCT05686564
NCT05686564No Longer Available不适用

Early Access Program for ALXN1840 in Patients With Wilson Disease

Alexion Pharmaceuticals, Inc.0 个研究点开始时间: 2023年1月17日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
No Longer Available

研究概览

简要总结

This is an open-label, single-arm, multi-center EAP, designed to provide early access to ALXN1840 for eligible patients with WD.

详细描述

To provide access to ALXN1840 treatment, an investigational medicinal product (IMP) that has not yet been granted marketing authorization, to participants who complete Studies ALXN1840-WD-205, WTX101-301, or ALXN1840-WD-302, or other studies with ALXN1840 who, in the opinion of the Treating Physician, may benefit from continued treatment with ALXN1840, and who meet the eligibility criteria described in this protocol.

研究设计

研究类型
Expanded Access

入排标准

年龄范围
3 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • ≥ 3 years of age or older at the time of providing informed consent/assent and expressed desire to continue treatment with ALXN
  • Confirmed diagnosis of WD.
  • Has completed one of the following ALXN1840 clinical studies:
  • ALXN1840-WD-205
  • ALXN1840-WD-302
  • Other ALXN1840 studies
  • In the Treating Physician's medical opinion, the potential benefits of treatment with ALXN1840 outweigh the potential risks for the participant.
  • Participant or legal representative provided informed consent/assent to be treated with ALXN1840 through this EAP.
  • Female participants of childbearing potential and male participants must follow protocol-specified-contraception guidance.

排除标准

  • Eligible for and able to participate in an Alexion-sponsored study of ALXN
  • Unwilling or unable to comply with the Treating Physician's treatment plan related to this EAP for any reason.
  • Has decompensated hepatic cirrhosis.
  • Model for End-Stage Liver Disease (MELD) score >
  • Modified Nazer Score >
  • End-stage renal disease on dialysis (chronic kidney disease stage 5 [CKD 5]) or creatinine clearance < 30 mL/min.
  • Known hypersensitivity to ALXN1840, ALXN1840 excipients, or any of the ingredients contained in ALXN
  • Women who are nursing or pregnant (or women who are planning to become pregnant during treatment with ALXN1840).

研究者

申办方类型
Industry
责任方
Sponsor

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