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临床试验/EUCTR2016-000942-77-DE
EUCTR2016-000942-77-DE进行中(未招募)1 期

A Phase 3 Randomized, Multicenter, Multinational, Double-blinded Study Comparing the Efficacy and Safety of Repeated Biweekly Infusions of Avalglucosidase Alfa (neoGAA, GZ402666) and Alglucosidase Alfa in Treatment naïve Patients with Late-onset Pompe Disease

Genzyme Corporation0 个研究点目标入组 100 人开始时间: 2016年6月27日最近更新:
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试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
100

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

  • -The patient has confirmed GAA enzyme deficiency from any tissue
  • source and/or 2 confirmed GAA gene mutations.
  • -The patient must provide signed, informed consent prior to performing
  • any study related procedures. Consent of a legally authorized
  • guardian(s) is (are) required for legally minor patients as defined by
  • local regulation. If the patient is legally minor, signed written consent
  • shall be obtained from parent(s)/legal guardian and assent obtained
  • from patients, if applicable.
  • -The patient (and patient's legal guardian if patient is legally minor as
  • defined by local regulation) must have the ability to comply with the
  • clinical protocol.
  • -The patient, if female and of childbearing potential, must have a
  • negative pregnancy test (beta-human chorionic gonadotropin) at
  • -The patient is <3 years of age.
  • -The patient has known Pompe specific cardiac hypertrophy.
  • -The patient is wheelchair dependent.
  • -The patient is not able to ambulate 40 meters (approximately 130 feet)
  • without stopping and without an assistive device.
  • -The patient requires invasive-ventilation (non-invasive ventilation is
  • -The patient is not able to successfully perform repeated forced vital
  • capacity (FVC) measurements in upright position of =30% predicted and
  • =85% predicted.
  • -The patient has had previous treatment with alglucosidase alfa or any
  • investigational therapy for Pompe disease.
  • -The patient has prior or current use of immune tolerance induction
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 7
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 122
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 17

排除标准

  • -The patient is <3 years of age.
  • -The patient has known Pompe specific cardiac hypertrophy.
  • -The patient is wheelchair dependent.
  • -The patient is not able to ambulate 40 meters (approximately 130 feet) without topping and without an assistive device.
  • -The patient requires invasive-ventilation (non-invasive ventilation is allowed).
  • -The patient is not able to successfully perform repeated forced vital capacity (FVC) measurements in upright position of =40% predicted and =85% predicted.
  • -The patient has had previous treatment with alglucosidase alfa or any investigational therapy for Pompe disease.
  • -The patient has prior or current use of immune tolerance induction therapy

研究者

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