Search for a clinical trial
Other search option(s)
69 Result(s)
Recruiting trial
= ; Ongoing trial
=
; Funded by an IRDiRC member =
; Member of a ERN =
National clinical trial(s)

Mecklenburg-Vorpommern
GREIFSWALD

Multicentre, randomized, double-blind, prospective investigation on the effects of Immunoadsorption on cardiac function in patients with Dilated Cardiomyopathy (Phase IV) - DE
Universitätsmedizin Greifswald
Klinik und Poliklinik für Innere Medizin B

EMILIA ROMAGNA
FERRARA

TITAN Study: Rapid Recovery of Left Ventricular Function in Patients With Takotsubo Syndrome Undergoing Systemic Infusion of Adenosine: a Randomized Controlled Trial
A.O.U. di Ferrara - Nuovo Ospedale S.Anna - Sede di Cona
Divisione di Cardiologia

AUVERGNE-RHONE-ALPES
ADDRESS: NOT PROVIDED - FR

An Open-Label, Dose-Escalation, Phase 1 Study of the Oral Formulation of MLN9708 Administered Weekly in Adult Patients With Relapsed or Refractory Light-Chain (AL) Amyloidosis Who Require Further Treatment - FR
Institution: Information not provided - FR

NOUVELLE AQUITAINE
LIMOGES
AmyDara: A Multicentre Open Label Phase II Study of Daratumumab in AL Amyloidosis Patients Not in VGPR or Better - FR
CHU de Limoges - Hôpital Dupuytren
Service d'hématologie clinique et de thérapie cellulaire

Baden-Württemberg
HEIDELBERG

The VITAL Amyloidosis Study: A Phase 3, Randomized, Multicenter, Double-Blind, Placebo-Controlled, 2-Arm, Efficacy and Safety Study of NEOD001 Plus Standard of Care Versus Placebo Plus Standard of Care in Subjects With Light-Chain (AL) Amyloidosis - DE
Zentrum für Innere Medizin (Krehl-Klinik)
Abteilung Innere Medizin V - Hämatologie, Onkologie und Rheumatologie

Baden-Württemberg
HEIDELBERG

A Phase 3 Randomized, Controlled, Open-label, Multicenter, Safety and Efficacy Study of Dexamethasone Plus MLN9708 or Physician's Choice of Treatment Administered to Patients With Relapsed or Refractory Systemic Light-Chain (AL) Amyloidosis - DE
Zentrum für Innere Medizin (Krehl-Klinik)
Abteilung Innere Medizin V - Hämatologie, Onkologie und Rheumatologie

Baden-Württemberg
HEIDELBERG

A randomized open-label multicenter phase III trial of melphalan and dexamethasone (MDex) versus bortezomib, melphalan and dexamethasone (BMDex) for untreated patients with systemic light-chain (AL) amyloidosis - DE
Zentrum für Innere Medizin (Krehl-Klinik)
Abteilung Innere Medizin V - Hämatologie, Onkologie und Rheumatologie

Baden-Württemberg
HEIDELBERG
An open-label, phase 1/2 study of melflufen and dexamethasone for patients with al amyloidosis following at least one prior line of therapy - DE
Zentrum für Innere Medizin (Krehl-Klinik)
Abteilung Innere Medizin V - Hämatologie, Onkologie und Rheumatologie

Nordrhein-Westfalen
MÜNSTER

An Open-Label Extension Study to Assess the Long-Term Safety and Efficacy of ISIS 420915 in Patients with Familial Amyloid Polyneuropathy (FAP) (Phase III) - FR
Universitätsklinikum Münster

EMILIA ROMAGNA
ADDRESS: NOT PROVIDED - IT

An Open-Label, Phase 1/2 Study of Melflufen and Dexamethasone for Patients with AL Amyloidosis Following at Least One Prior Line of Therapy - IT
Institution: Information not provided - IT

LOMBARDIA
PAVIA

A randomized open-label multicenter phase III trial of melphalan and dexamethasone (MDex) versus bortezomib, melphalan and dexamethasone (BMDex) for untreated patients with systemic light-chain (AL) amyloidosis - IT
Fondazione IRCCS Policlinico San Matteo
Laboratorio di Biotecnologie e Tecnologie Biomediche

LOMBARDIA
PAVIA

A Single Center, Twelve-month, Open-label, Prospective Study Followed by a Six-month Withdrawal Period to Evaluate the Efficacy, Tolerability, Safety and Pharmacokinetics of Doxycycline in Combination With Tauroursodeoxycholic Acid in Transthyretin Amyloidosis
Fondazione IRCCS Policlinico San Matteo
Laboratorio di Biotecnologie e Tecnologie Biomediche

LOMBARDIA
PAVIA


A Randomized Phase II/III Trial of Doxycycline vs. Standard Supportive Therapy in Newly-diagnosed Cardiac AL Amyloidosis Patients Undergoing Bortezomib-based Therapy - IT
Fondazione IRCCS Policlinico San Matteo
Dipartimento di Medicina Molecolare

NORTE
PORTO

Trial to Evaluate Safety and Tolerability of ALN-TTR01 in Transthyretin (TTR) Amyloidosis (Phase I)
Hospital de Santo António - Centro Hospitalar do Porto
Unidade Clínica de Paramiloidose

NORTE
PORTO
Open-Label Safety and Efficacy Evaluation of Fx-1006A in Patients With Transthyretin Amyloidosis (Phase II/III)
Hospital de Santo António - Centro Hospitalar do Porto
Unidade Clínica de Paramiloidose

SUL
LISBOA
Open-Label Safety and Efficacy Evaluation of Fx-1006A in Patients With Transthyretin Amyloidosis (Phase II/III)
Hospital de Sta. Maria - Centro Hospitalar de Lisboa Norte, EPE.
Serviço de Neurologia

Andalucía
HUELVA
An Open-label Study to Evaluate Safety, Efficacy and Pharmacokinetics (PK) of Patisiran-LNP in Patients with Hereditary Transthyretin-mediated Amyloidosis (hATTR amyloidosis) with Disease Progression Post-Orthotopic Liver Transplant (Phase III) - ES
Hospital Juan Ramón Jiménez

Cataluña
BARCELONA
A Phase 3 Randomized, Controlled, Open-label, Multicenter, Safety and Efficacy Study of Dexamethasone Plus MLN9708 or Physician's Choice of Treatment Administered to Patients With Relapsed or Refractory Systemic Light Chain (AL) Amyloidosis - ES
Hospital Clínic de Barcelona
Servicio de Hematología

Cataluña
BARCELONA

An open-label, phase 1/2 study of melflufen and dexamethasone for patients with al amyloidosis following at least one prior line of therapy - ES
Hospital Clínic de Barcelona
Servicio de Hematología

Cataluña
BARCELONA


ReDox: A randomized phase II/III trial of doxycycline vs. standard supportive therapy in newly-diagnosed cardiac AL amyloidosis patients undergoing bortezomib-based therapy - ES
Hospital Clínic de Barcelona
Servicio de Hematología

Cataluña
L'HOSPITALET DE LLOBREGAT
An Open-label Study to Evaluate Safety, Efficacy and Pharmacokinetics (PK) of Patisiran-LNP in Patients with Hereditary Transthyretin-mediated Amyloidosis (hATTR amyloidosis) with Disease Progression Post-Orthotopic Liver Transplant (Phase III) - ES
Hospital Universitari de Bellvitge

Greater London
LONDON
A randomized open-label multicenter phase III trial of Melphalan and Dexamethasone (MDex) versus Bortezomib, Melphalan and Dexamethasone (BMDex) for untreated patients with systemic light-chain (AL) amyloidosis - UK
Joint UCLH/UCL Biomedical Research and Development (R&D) Unit
University College London (UCL) and University College London Hospitals NHS Trust (UCLH)

West Midlands
BIRMINGHAM

Massachusetts
CAMBRIDGE

A Phase 1, Randomized, Single-Blind, Placebo Controlled, Single-Ascending Dose, Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics Study of Subcutaneously Administered ALN-TTRSC02 in Healthy Subjects
Alnylam Pharmaceuticals, Inc.

WIEN
ADDRESS: NOT PROVIDED - AT

CARDIO-TTRansform: A Phase 3 Global, Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Efficacy and Safety of ION-682884 in Patients With Transthyretin-Mediated Amyloid Cardiomyopathy (ATTR CM) - AT
Institution: Information not provided - AT

WIEN
ADDRESS: NOT PROVIDED - AT

HELIOS-B: A Phase 3, Randomized, Double-blind, Placebo-controlled, Multicenter Study to Evaluate the Efficacy and Safety of Vutrisiran in Patients With Transthyretin Amyloidosis With Cardiomyopathy (ATTR Amyloidosis With Cardiomyopathy) - AT
Institution: Information not provided - AT

ILE-DE-FRANCE
LE KREMLIN-BICÊTRE


A Phase 2/3 Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy and Safety of ISIS 420915 in Patients With Familial Amyloid Polyneuropathy - FR
CHU Paris-Sud - Hôpital de Bicêtre
Service de neurologie - CRMR NNERf

ILE-DE-FRANCE
LE KREMLIN-BICÊTRE

APOLLO: A Phase 3 Multicenter, Multinational, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of ALN-TTR02 in Transthyretin (TTR)-Mediated Polyneuropathy (Familial Amyloidotic Polyneuropathy-FAP) - FR
CHU Paris-Sud - Hôpital de Bicêtre
Service de neurologie - CRMR NNERf

ILE-DE-FRANCE
LE KREMLIN-BICÊTRE

A Multicenter, Open-Label, Extension Study to Evaluate the Long-term Safety and Efficacy of Patisiran in Patients With Familial Amyloidotic Polyneuropathy Who Have Completed a Prior Patisiran Clinical Study (Phase III) - FR
CHU Paris-Sud - Hôpital de Bicêtre
Service de neurologie - CRMR NNERf

ILE-DE-FRANCE
LE KREMLIN-BICÊTRE

An Open-Label Extension Study to Assess the Long-Term Safety and Efficacy of ISIS 420915 in Patients with Familial Amyloid Polyneuropathy (FAP) (Phase III) - FR
CHU Paris-Sud - Hôpital de Bicêtre
Service de neurologie - CRMR NNERf

Baden-Württemberg
HEIDELBERG

A multicentre, international, phase 3, double-blind, placebo-controlled, randomized study to evaluate the efficacy, safety and tolerability of daily oral dosing of tafamidis meglumine (PF-06291826) 20 mg or 80 mg in comparison to placebo in subjects diagnosed with transthyretin cardiomyopathy - DE
Zentrum für Innere Medizin (Krehl-Klinik)
Abteilung Innere Medizin V - Hämatologie, Onkologie und Rheumatologie

Baden-Württemberg
HEIDELBERG
A Phase 3 Multicenter, Multinational, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of ALN TTRSC in Patients With Transthyretin (TTR) Mediated Familial Amyloidotic Cardiomyopathy (FAC) - DE
Zentrum für Innere Medizin (Krehl-Klinik)
Abteilung Innere Medizin V - Hämatologie, Onkologie und Rheumatologie

Nordrhein-Westfalen
MÜNSTER
APOLLO: A Phase 3 multicenter, multinational, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of Patisiran (ALN-TTR02) in Transthyretin (TTR)-Mediated Polyneuropathy (Familial amyloid polyneuropathy-FAP) - DE
Universitätsklinikum Münster
Medizinische Klinik B für Gastroenterologie und Hepatologie

Nordrhein-Westfalen
MÜNSTER

A Phase III, Multicenter, Open-Label, Extension Study to Evaluate the Long-term Safety and Efficacy of Patisiran in Patients With Familial Amyloidotic Polyneuropathy Who Have Completed a Prior Patisiran Clinical Study (Enrolling only by invitation) - DE
Universitätsklinikum Münster
Medizinische Klinik B für Gastroenterologie und Hepatologie

Andalucía
HUELVA
A Multicenter, Open-Label, Extension Study to Evaluate the Long-term Safety and Efficacy of Patisiran in Patients with Familial Amyloidotic Polyneuropathy Who Have Completed a Prior Clinical Study with Patisiran (Phase III) - ES
Hospital Juan Ramón Jiménez
Servicio de Medicina Interna

Andalucía
MÁLAGA

HELIOS-B: A Phase 3, Randomized, Double-blind, Placebo-controlled, Multicenter Study to Evaluate the Efficacy and Safety of Vutrisiran in Patients with Transthyretin Amyloidosis with Cardiomyopathy (ATTR Amyloidosis with Cardiomyopathy) - ES
Hospital Universitario Virgen de la Victoria
Unidad de Corazón y Patología Cardiovascular

Baleares
PALMA DE MALLORCA
A Multicenter, Open-Label, Extension Study to Evaluate the Long-term Safety and Efficacy of Patisiran in Patients with Familial Amyloidotic Polyneuropathy Who Have Completed a Prior Clinical Study with Patisiran (Phase III) - ES
Hospital Son Llàtzer
Unidad de Medicina Interna

Cataluña
BARCELONA

An Open-Label Extension Study to Assess the Long-Term Safety and Efficacy of ISIS 420915 in Patients with Familial Amyloid Polyneuropathy (FAP) (Phase III) - ES
Hospital Clínic de Barcelona

Cataluña
BARCELONA
A Multicenter, Open-Label, Extension Study to Evaluate the Long-term Safety and Efficacy of Patisiran in Patients with Familial Amyloidotic Polyneuropathy Who Have Completed a Prior Clinical Study with Patisiran (Phase III) - ES
Hospital Clínic de Barcelona
Instituto Clínic de Nefrología y Urología

Cataluña
BARCELONA

An Open-Label Extension Study to Assess the Long-Term Safety and Efficacy of ISIS 420915 in Patients with Familial Amyloid Polyneuropathy (FAP) (Phase III) - ES
Hospital Universitari Vall d'Hebron

Cataluña
BARCELONA

HELIOS-B: A Phase 3, Randomized, Double-blind, Placebo-controlled, Multicenter Study to Evaluate the Efficacy and Safety of Vutrisiran in Patients with Transthyretin Amyloidosis with Cardiomyopathy (ATTR Amyloidosis with Cardiomyopathy) - ES
Hospital Universitari Vall d'Hebron
Servicio de Medicina Interna

Cataluña
L'HOSPITALET DE LLOBREGAT

HELIOS-B: A Phase 3, Randomized, Double-blind, Placebo-controlled, Multicenter Study to Evaluate the Efficacy and Safety of Vutrisiran in Patients with Transthyretin Amyloidosis with Cardiomyopathy (ATTR Amyloidosis with Cardiomyopathy) - ES
Hospital Universitari de Bellvitge
Servicio de Cardiología

Comunidad Valenciana
VALENCIA
HELIOS-A: A Phase 3 Global, Randomized, Open-label Study to Evaluate the Efficacy and Safety of ALN-TTRSC02 in Patients with Hereditary Transthyretin Amyloidosis (hATTR Amyloidosis) - ES
Hospital Universitario y Politécnico La Fe
Servicio de Neurología

Galicia
A CORUÑA

A phase 3 multicenter, randomized, double-blind, extension study to evaluate the safety of daily oral dosing of tafamidis meglumine (PF-06291826) 20 mg or 80 mg in subjects diagnosed with transthyretin cardiomyopathy (TTR-CM) - ES
Hospital Universitario da Coruña

Madrid
ADDRESS: NOT PROVIDED - ES
ATTRIBUTE-CM Trial: A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study of the Efficacy and Safety of AG10 in Subjects with Symptomatic Transthyretin Amyloid Cardiomyopathy - ES
Institution: Information not provided - ES

Madrid
ADDRESS: NOT PROVIDED - ES
A Randomized Phase 3 Study to Evaluate the Efficacy and Safety of Daratumumab in Combination with Cyclophosphamide, Bortezomib and Dexamethasone (CyBorD) Compared With CyBorD Alone in Newly Diagnosed Systemic AL Amyloidosis - ES
Institution: Information not provided - ES

Madrid
MADRID
A Multicenter, Open-Label, Extension Study to Evaluate the Long-term Safety and Efficacy of Patisiran in Patients with Familial Amyloidotic Polyneuropathy Who Have Completed a Prior Clinical Study with Patisiran (Phase III) - ES
Hospital Clínico San Carlos

Madrid
MADRID


AMILCA-DIFLU: Unicentre, open, uncontrolled clinical trial to assess the morphological, biochemical and functional effects of Diflunisal treatment in patients with transthyretin cardiac amyloidosis (Phase II-III) - ES
Hospital Universitario Fundación Jiménez Díaz
Servicio de Cardiología

Madrid
MAJADAHONDA

A phase 3 multicenter, randomized, double-blind, extension study to evaluate the safety of daily oral dosing of tafamidis meglumine (PF-06291826) 20 mg or 80 mg in subjects diagnosed with transthyretin cardiomyopathy (TTR-CM) - ES
Hospital Universitario Puerta de Hierro - Majadahonda

Madrid
MAJADAHONDA

CARDIO-TTRansform: A Phase 3 Global, Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Efficacy and Safety of ION-682884 in Patients with Transthyretin-Mediated Amyloid Cardiomyopathy (ATTR CM) - ES
Hospital Universitario Puerta de Hierro - Majadahonda
Servicio de Cardiología

Madrid
MAJADAHONDA

HELIOS-B: A Phase 3, Randomized, Double-blind, Placebo-controlled, Multicenter Study to Evaluate the Efficacy and Safety of Vutrisiran in Patients with Transthyretin Amyloidosis with Cardiomyopathy (ATTR Amyloidosis with Cardiomyopathy) - ES
Hospital Universitario Puerta de Hierro - Majadahonda
Servicio de Cardiología

Murcia
EL PALMAR, MURCIA

CARDIO-TTRansform: A Phase 3 Global, Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Efficacy and Safety of ION-682884 in Patients with Transthyretin-Mediated Amyloid Cardiomyopathy (ATTR CM) - ES
Hospital Clínico Universitario Virgen de la Arrixaca
Servicio de Cardiología

Region Västerbotten
UMEÅ
Safety and Efficacy of Orally Administered Fx-1006A in Patients With Familial Amyloid Polyneuropathy (FAP): A Randomized, Double-Blind, Placebo-Controlled Study (Phase II-III)
University Hospital of Umeå
Department of Medicine

Greater London
LONDON
A Pilot study of Response to Velcade combination chemotherapy in AL amyloidosis (REVEAL)
Cancer Research UK & UCL Cancer Trials Centre

Greater London
LONDON

A multicentre, international, phase 3, double-blind, placebo-controlled, randomized study to evaluate the efficacy, safety and tolerability of daily oral dosing of tafamidis meglumine (PF-06291826) 20 mg or 80 mg in comparison to placebo in subjects diagnosed with transthyretin cardiomyopathy (TTR-CM) - UK
St George's Healthcare NHS Trust
Department of Haematology

Greater London
LONDON


ISIS 420915-CS2: A Phase 2/3 Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy and Safety of ISIS 420915 in Patients With Familial Amyloid Polyneuropathy - UK
University College London Medical School and Royal Free Hospital
National Amyloidosis Centre, Division of Medicine

Greater Manchester
ADDRESS: NOT PROVIDED - UK
An Open-Label Extension Study to Assess the Long-Term Safety and Efficacy of ISIS 420915 in Patients with Familial Amyloid Polyneuropathy (FAP) - GB
Institution: Information not provided - UK

Massachusetts
CAMBRIDGE
Fx-005: Safety and efficacy of Orally Administered Fx-1006A in Patients with Familial Amyloid Polyneuropathy (FAP): a Phase II/III, Randomised, Double-Blind, Placebo-Controlled Study - UK
FoldRx Pharmaceuticals, Inc.
FoldRx Pharmaceuticals

New York
NEW YORK


An Open-Label Extension Study to Assess the Long-Term Safety and Efficacy of ISIS 420915 in Patients With Familial Amyloid Polyneuropathy (FAP) (Phase III) - US
Icahn School of Medicine at Mount Sinai

Washington
ADDRESS: NOT PROVIDED - US


A Phase 2/3 Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy and Safety of ISIS 420915 in Patients With Familial Amyloid Polyneuropathy - US
Institution: Information not provided - US
Multinational clinical trial(s)

ILE-DE-FRANCE
PARIS
Determination of the efficacious and safe dose of Ivabradine in paediatric patients with Dilated Cardiomyopathy and symptomatic chronic heart failure aged from 6 months to less than 18 years (Phase II/III)
Hôpital Necker-Enfants Malades
Cardiologie pédiatrique : Unité médico-chirurgicale de cardiologie congénitale et pédiatrique

County Dublin
ADDRESS: NOT PROVIDED - IE
A Phase 2b Open-label Extension Study to Evaluate the Long-term Safety and Efficacy of NEOD001 in Subjects with Light Chain (AL) Amyloidosis who were previously enrolled in Study NEOD001-201 (Prematurely ended)
Institution: Information not provided - IE

LOMBARDIA
PAVIA
A Randomized Phase II/III Trial of Doxycycline vs. Standard Supportive Therapy in Newly-diagnosed Cardiac AL Amyloidosis Patients Undergoing Bortezomib-based Therapy
Fondazione IRCCS Policlinico San Matteo
Dipartimento di Medicina Molecolare

Region Stockholm
STOCKHOLM
An Open-Label, Phase 1/2 Study of Melflufen and Dexamethasone for Patients with AL Amyloidosis Following at Least One Prior Line of Therapy
Oncopeptides AB

Massachusetts
CAMBRIDGE
A Phase 2, Open-Label, Multi-Dose, Dose Escalation Trial to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Intravenous Infusions of ALN-TTR02 in Patients With TTR Amyloidosis - coordination
Alnylam Pharmaceuticals, Inc.

Massachusetts
CAMBRIDGE
An Open-label Study to Evaluate Safety, Efficacy and Pharmacokinetics (PK) of Patisiran-LNP in Patients With Hereditary Transthyretin-mediated Amyloidosis (hATTR Amyloidosis) With Disease Progression Post-Orthotopic Liver Transplant
Alnylam Pharmaceuticals, Inc.

Washington
ADDRESS: NOT PROVIDED - US
AMYDARA: A Multicentre Open Label Phase II Study of Daratumumab in AL Amyloidosis Patients Not in VGPR or Better
Institution: Information not provided - US

Massachusetts
CAMBRIDGE
A Phase 2, Multicenter, Open-Label, Extension Study to Evaluate the Long-Term Safety, Clinical Activity, and Pharmacokinetics of ALN-TTR02 in Patients With Familial Amyloidotic Polyneuropathy Who Have Previously Received ALN-TTR02
Alnylam Pharmaceuticals, Inc.

Massachusetts
CAMBRIDGE