EUCTR2019-000954-67-BE进行中（未招募）1 期
A Phase 3 Open-label Extension Study to Assess the Long-term Safety and Efficacy of Intravenous ATB200 Co-administered With Oral AT2221 in Adult Subjects With Late-onset Pompe Disease
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 110
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
- •Subjects Who Participated in Study ATB200-03:
- •1. Subject must provide signed informed consent prior to any study-related procedures being performed. If the subject is under 20 years of age, the subject must provide written informed consent.
- •2. Subject must have completed Study ATB200-03.
- •Note: Subjects who were forced to withdraw from Study ATB200-03 for a logistical reason not related to the efficacy or safety of ATB200/AT2221 (eg, hospitalization for a car accident, COVID-19 pandemic, or emergency surgery) and which resulted in several consecutive missed doses may be eligible to participate in this study upon approval by the Amicus medical monitor.
- •3. Female subjects of childbearing potential and male subjects must agree to use medically accepted methods of contraception during the study and for 90 days after the last dose of study drug.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 92
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 18
排除标准
- •Subjects Who Participated in Study ATB200-03:
- •1. Subject plans to receive gene therapy or participate in another interventional study for Pompe disease.
- •2. Subject has a hypersensitivity to any of the excipients in ATB200 or AT2221, or has a medical condition or any other extenuating circumstance that may, in the opinion of the investigator or medical monitor, pose an undue safety risk to the subject or may compromise his/her ability to comply with or adversely impact protocol requirements. This includes clinical depression (as diagnosed by a psychiatrist or other mental health professional) with uncontrolled or poorly controlled symptoms.
- •3. Subject, if female, is pregnant or breastfeeding.
- •4. Subject, whether male or female, is planning to conceive a child during the study.
研究者
相似试验
进行中（未招募）
1 期
A study investigating the long-term safety and efficacy of intravenous (IV) ATB200 when Co-administrated with oral AT2221 in adult subjects with Pompe diseaseAdult Subjects With Late Onset Pompe Disease (LOPD)MedDRA version: 24.0Level: LLTClassification code 10075702Term: Pompe's disease late onsetSystem Organ Class: 100000004850EUCTR2019-000954-67-ITAMICUS THERAPEUTICS, INC.120
招募中
3 期
A Phase 3 Open-label Extension Study to Assess the Long-term Safety and Efficacy of Intravenous ATB200 Co-administered With Oral AT2221 in Adult Subjects With Late-onset Pompe DiseaseGlycogen storage disease type II10028396Pompe diseaseNL-OMON54552Amicus Therapeutics1
进行中（未招募）
3 期
ATB200/AT2221 Phase 3 Open-label Extension StudyPompe diseaseJPRN-jRCT2011200003Wright Jacquelyn110
进行中（未招募）
1 期
A study investigating the long-term safety and efficacy of intravenous (IV) ATB200 when Co-administrated with oral AT2221 in adult subjects with Pompe diseaseEUCTR2019-000954-67-GBAmicus Therapeutics, Inc.110
进行中（未招募）
1 期
A study investigating the long-term safety and efficacy of intravenous (IV) ATB200 when Co-administrated with oral AT2221 in adult subjects with Pompe diseaseEUCTR2019-000954-67-GRAmicus Therapeutics, Inc.110