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Showing 20 of 47 recruiting trials for “fabry-disease

EARLY_Phase 1RecruitingNCT06207552

Evaluation of the Safety, Tolerability and Efficacy of a Gene Therapy Drug for the Treatment of Pediatric Fabry Disease

👨‍⚕️ Hong Xu, MD,PhD, Children's Hospital of Fudan University📍 1 site📅 Started Feb 2024View details ↗
NARecruitingNCT06368076

High-intensity Interval Training in Patients With Spinal Muscular Atrophy

👨‍⚕️ John Vissing, prof. MD, Rigshospitalet, Denmark📍 1 site📅 Started Jan 2024View details ↗
NARecruitingNCT06322654

A Head-to-head Study Comparing the Functional Value of Two Models of Robotically Assisted Rehabilitation in SMA (Spinal Muscular Atrophy) Patients

👨‍⚕️ Marek Jóźwiak, Wiktor Dega University Orthopedic and Rehabilitation Hospital📍 1 site📅 Started Dec 2023View details ↗
RecruitingNCT05994950

A Review of the Management and Outcomes of Children With SMA in the West Midlands During 2017-2022

🏥 Robert Jones and Agnes Hunt Orthopaedic and District NHS Trust📍 2 sites📅 Started Dec 2023View details ↗
NARecruitingNCT05866419

Study of an Intrathecal Port and Catheter System for Subjects With Spinal Muscular Atrophy

🏥 Alcyone Therapeutics, Inc📍 21 sites📅 Started Nov 2023View details ↗
Phase 2RecruitingNCT06114329

Study of the Safety and Biologic Activity of AL01211 in Treatment Naive Males With Classic Fabry Disease

👨‍⚕️ Nan Chen, Dr., Ruijin Hospital📍 6 sites📅 Started Oct 2023View details ↗
NARecruitingNCT06095713

German Observational Multicenter Study of Patients With Fabry Disease Under Enzyme Replacement Therapy With Pegunigalsidase-alfa

👨‍⚕️ Eva Brand, MD, PhD, Universitätsklinikum Münster📍 8 sites📅 Started Oct 2023View details ↗
NARecruitingNCT05698901

Biomarkers and Cardiac Imaging Diagnostic Assay for Monitoring Patients With Fabry Disease

👨‍⚕️ Charles Jia-Yin Hou, Mackay Memorial Hospital📍 1 site📅 Started Sep 2023View details ↗
NARecruitingNCT05923788

T1 Mapping in Fabry Disease

👨‍⚕️ SANDRINE LEMOINE, PU-PH📍 2 sites📅 Started Aug 2023View details ↗
Phase 2, PHASE3RecruitingNCT05710692

Study to Evaluate the Safety, PK, PD, and Efficacy of PRX-102 in Japanese Patients With Fabry Disease

🏥 Chiesi Farmaceutici S.p.A.📍 10 sites📅 Started Aug 2023View details ↗
RecruitingNCT06610019

Cardiovascular Multimodality Imaging Study

👨‍⚕️ Leandro Slipczuk, MD, PhD, Montefiore Medical Center📍 1 site📅 Started May 2023View details ↗
Phase 3RecruitingNCT06081062

Evaluate the Safety and Efficacy of Fabagal® (Agalsidase Beta) in Patients With Fabry Disease

🏥 ISU Abxis Co., Ltd.📍 3 sites📅 Started Apr 2023View details ↗
Phase 1, PHASE2RecruitingNCT05824169

Evaluation of Safety and Efficacy of Gene Therapy Drug in the Treatment of Spinal Muscular Atrophy (SMA) Type 1 Patients

🏥 GeneCradle Inc📍 4 sites📅 Started Feb 2023View details ↗
Phase 4RecruitingNCT05067868

A Study of Replagal in Children and Adults With Fabry Disease in India

👨‍⚕️ Study Director, Takeda📍 3 sites📅 Started Nov 2022View details ↗
Phase 1, PHASE2RecruitingNCT05629559

4D-310 in Adults With Fabry Disease and Cardiac Involvement

👨‍⚕️ Alan H Cohen, MD, 4D Molecular Therapeutics📍 4 sites📅 Started Oct 2022View details ↗
NARecruitingNCT06806813

Italian Anderson Fabry Disease Cardiovascular Registry

👨‍⚕️ Elena Biagini, MD, PhD, IRCCS Azienda Ospedaliero-Universitaria di Bologna📍 20 sites📅 Started Jan 2022View details ↗
NARecruitingNCT05638750

Outpatient Rehabilitation Intervention for Young Children With SMA

🏥 Holland Bloorview Kids Rehabilitation Hospital📍 1 site📅 Started Jan 2022View details ↗
Enrolling by InvitationNCT05039866

Long-Term Follow-up of Subjects Who Were Treated With ST-920

👨‍⚕️ Medical Monitor, Sangamo Therapeutics, Inc.📍 13 sites📅 Started Aug 2021View details ↗
NARecruitingNCT04856059

Fabry Cardiomyopathy: Identification of Early Myocardial Structural and Tissue Abnormalities Using Multiparametric MRI

👨‍⚕️ Kate Hanneman, University Health Network, Toronto📍 1 site📅 Started Jun 2021View details ↗
NARecruitingNCT04440254

Long Duration Holter ECG in Fabry Disease

👨‍⚕️ Albert HAGEGE, Dr📍 1 site📅 Started May 2021View details ↗
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