Suche klinische Studie
Weitere Suchoptionen
23 Ergebnis(se)
Rekrutierende Studie = ; Fortlaufende Studie =
; Abgeschlossene Studie =
; Förderung durch ein IRDiRC-Mitglied =
; Studie unter Beteiligung von ERN-Mitgliedern aus mindestens zwei Mitgliedstaaten =
Nationale klinische Studie(n)

ANTWERPEN
EDEGEM (ANTWERPEN)
ATTRACT study: A randomized, open-label study to compare the efficacy and safety of AT1001 and enzyme replacement therapy (ERT) in patients with Fabry disease and AT1001-responsive GLA mutations, who were previously treated with ERT - BE
Antwerp University Hospital - UZA
CEMA - Centrum voor Erfelijke Metabole Aandoeningen

ANTWERPEN
EDEGEM (ANTWERPEN)
An Open-Label Extension Study to Evaluate the LongTerm Safety and Efficacy of Migalastat Hydrochloride Monotherapy in Subjects With Fabry Disease (Phase III) - BE
Antwerp University Hospital - UZA
Department of pediatric metabolic diseases (Metabole stoornissen kinderen/Metabolic Disorders in Children)

Bayern
OCHSENFURT
Eine doppelblinde, randomisierte, Placebo-kontrollierte Studie zur Untersuchung der Wirksamkeit, Sicherheit und Pharmakodynamik von AT1001 bei Patienten mit Fabry-Krankheit und einer GLA-Mutation, die auf AT1001 anspricht (Phase III)
Facharztpraxis für innere Medizin und Nephrologie

Berlin
ADDRESS: NOT PROVIDED - DE
ATTRACT: Eine randomisierte offene Studie zum Vergleich der Wirksamkeit und Sicherheit von AT1001 und einer Enzymersatztherapie (EET) bei Patienten mit Fabry-Krankheit und einer GLA-Mutation, die auf AT1001 anspricht (Phase III)
Institution: Information not provided - DE

ILE-DE-FRANCE
GARCHES
A 24-Week Safety and Pharmacodynamic Study of AT1001 in Patients With Fabry Disease (Phase II) - Terminated -
CHU Paris IdF Ouest - Hôpital Raymond Poincaré
Service de Génétique Médicale - Centre de référence Maladies Rares

ILE-DE-FRANCE
GARCHES
A 12-Week Safety and Pharmacodynamic Study of AT1001 in Female Patients With Fabry Disease (Phase II) - Terminated -
CHU Paris IdF Ouest - Hôpital Raymond Poincaré
Service de Génétique Médicale - Centre de référence Maladies Rares

ILE-DE-FRANCE
GARCHES
A double-blind, randomized, placebo-controlled study to evaluate the efficacy, safety and pharmacodynamics of AT1001 in patients with Fabry disease and AT1001-responsive GLA mutations (Phase III) - FR
CHU Paris IdF Ouest - Hôpital Raymond Poincaré
Service de Génétique Médicale - Centre de référence Maladies Rares

Noord-Holland
AMSTERDAM
A Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Efficacy, Safety and Pharmacodynamics of AT1001 in Patients With Fabry Disease and AT1001-Responsive GLA Mutations (Phase III) - NL
Amsterdam UMC
Afdeling Erfelijke Stofwisselingsziekten

Noord-Holland
AMSTERDAM
An Open-label Phase 2A Study to Investigate Drug-Drug Interactions Between AT1001 and Agalsidase in Subjects With Fabry Disease
Amsterdam UMC
Afdeling Erfelijke Stofwisselingsziekten

WIEN
ADDRESS: NOT PROVIDED - AT
An Open-Label Extension Study to Evaluate the Long Term Safety and Efficacy of Migalastat Hydrochloride Monotherapy in Subjects With Fabry Disease (Phase 3) - AT
Institution: Information not provided - AT

WIEN
ADDRESS: NOT PROVIDED - AT
ATTRACT: A Randomized, Open-Label Study to Compare the Efficacy and Safety of AT1001 and Enzyme Replacement Therapy (ERT) in Patients With Fabry Disease and AT1001-Responsive GLA Mutations, Who Were Previously Treated With ERT (Phase 3) - AT
Institution: Information not provided - AT

Warszawa
WARSAW
A double-blind, randomized, placebo-controlled study to evaluate the efficacy, safety and pharmacodynamics of AT1001 in patients with Fabry disease and AT1001-responsive GLA mutations (Phase III) - PL
Instytut Kardiologii im. Prymasa Tysiaclecia Stefana Kardynala Wyszynskiego
Klinika Kardiologii i Angiologii Interwencyjnej

Aragón
ZARAGOZA
A double-blind, randomized, placebo-controlled study to evaluate the efficacy, safety and pharmacodynamics of AT1001 in patients with Fabry disease and AT1001-responsive GLA mutations - ES (completed)
Hospital Universitario Miguel Servet
Servicio de Hematología y Hemoterapia

Aragón
ZARAGOZA
An Open-Label Extension Study to Evaluate the LongTerm Safety and Efficacy of Migalastat Hydrochloride Monotherapy in Subjects With Fabry Disease - ES (Completed)
Hospital Universitario Miguel Servet
Servicio de Hematología y Hemoterapia

Cataluña
BARCELONA
A double-blind, randomized, placebo-controlled study to evaluate the efficacy, safety and pharmacodynamics of AT1001 in patients with Fabry disease and AT1001-responsive GLA mutations - ES (completed)
Fundació Puigvert
Servicio de Nefrología

Cataluña
BARCELONA
An Open-Label, Extension Study to Evaluate the Long Term Safety and Efficacy of Migalastat Hydrochloride Monotherapy in subjects with Fabry Disease - ES (Completed)
Fundació Puigvert
Servicio de Nefrología

Madrid
ADDRESS: NOT PROVIDED - ES
An open-label study of the safety, pharmacokinetics, pharmacodynamics, and efficacy of 12-month treatment with migalastat in pediatric subjects (aged 12 to <18 years) with fabry disease and amenable GLA variants - ES (completed)
Institution: Information not provided - ES

Madrid
ADDRESS: NOT PROVIDED - ES

An Open-label Study to Evaluate the Safety and Pharmacokinetics of Migalastat HCl in Subjects With Fabry Disease and Amenable GLA Variants and Severe Renal Impairment or End-Stage Renal Disease Treated With Hemodialysis -ES
Institution: Information not provided - ES

Greater London
LONDON
Open-Label Extension Study to Evaluate the Long-Term Safety, Tolerability and Pharmacodynamics of AT1001 in Patients With Fabry Disease (Phase II)
Royal Free Hospital
Lysosomal storage disorders unit, Dept. of Haematology

Greater Manchester
ADDRESS: NOT PROVIDED - UK
A randomized, open-label study to compare the efficacy and safety of AT1001 and enzyme replacement therapy (ERT) in patients with Fabry disease and AT1001-responsive GLA mutations, who were previously treated with ERT (phase III) - UK
Institution: Information not provided - UK

Greater Manchester
ADDRESS: NOT PROVIDED - UK
A double-blind, randomized, placebo-controlled study to evaluate the efficacy, safety and pharmacodynamics of AT1001 in patients with Fabry disease and AT1001-responsive GLA mutations (Phase III) - UK
Institution: Information not provided - UK

Greater Manchester
SALFORD
FAB-CL-204: A Phase 2, Open-Label, Multiple Dose Level, 12-Week Study to Evaluate the Safety, Tolerability, and Pharmacodynamics of AT1001 in Female Patients With Fabry Disease
Hope Hospital, University of Manchester
Department of Metabolic Disease

Greater Manchester
SALFORD