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临床试验/CTIS2024-514773-22-00
CTIS2024-514773-22-00进行中(未招募)1 期

A French multicenter Phase 4 open label extension study of long-term safety and efficacy in patients with Pompe disease who previously participated in avalglucosidase development studies in France - PTA17333

Sanofi Winthrop Industrie0 个研究点目标入组 18 人开始时间: 2024年6月27日最近更新:

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
18

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

年龄范围
0 至 65+(—)
性别
All

入选标准

  • Patient with LOPD or IOPD who has previously completed Study EFC14028, LTS13769, or ACT14132 in France, and reimbursement for avalglucosidase alfa is not yet granted in France., The patient and/or their parent/legal guardian is willing and able to provide signed informed consent, and the patient, if <18 years of age, is willing to provide assent if deemed able to do so., The patient (and patient's legal guardian if patient is <18 years of age) must have the ability to comply with the clinical protocol., The patient, if female and of childbearing potential, must have a negative pregnancy test result [urine beta-human chorionic gonadotropin (ß-HCG)] at enrollment., Sexually active female patients of childbearing potential and male patients are required to practice true abstinence in line with their preferred and usual lifestyle or to use 2 acceptable effective methods of contraception.

排除标准

  • Patient with life-threatening hypersensitivity (anaphylactic reaction) to one of avalglucosidase alfa's excipients., Patient who permanently discontinued avalglucosidase alfa in a previous clinical study, Pregnant or breastfeeding female patient, The patient is concurrently participating in another clinical study of investigational treatment, The patient, in opinion of the Investigator, is unable to comply with the requirements of the study, The patient has clinically significant organic disease (with the exception of symptoms relating to Pompe disease), including clinically significant cardiovascular, hepatobiliary, pulmonary, neurologic, or renal disease, or other medical condition, serious intercurrent illness, or extenuating circumstance that, in the opinion of the Investigator, precludes participation in the study or potentially decreases survival., Individuals accommodated in an institution because of regulatory or legal order; prisoners, or patients who are legally institutionalized.

研究者

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