Clinical Trials on Hereditary Angioedema in France

Total 392 results

Fondation Ophtalmologique Adolphe de Rothschild

Completed

Genetic Analysis and Multimodal Retinal Imaging of Asymptomatic Fovea Plana Cases in the General Population (APOGEE)

Albinism | Fovea Plana

France
Hospices Civils de Lyon

Completed

Diagnostic Value of Ultra-low Dose Thoracic Scanner for the Pulmonary Arteriovenous Malformation Detection in HHT Patient (ULD OSLER)

Telangiectasia, Hereditary Hemorrhagic | Rendu Osler Disease

France
University Hospital, Montpellier
Ministry of Health, France

Completed

Autosomal Dominant Retinitis Pigmentosa: Prevalence of Known Genes Identification of New Loci / Genes

Autosomal Dominant Retinitis Pigmentosa

France
University Hospital, Bordeaux

Recruiting

NGS Panel of Incomplete Forms of Ocular Albinism (DIA)

Albinism, Ocular

France
Fondation Ophtalmologique Adolphe de Rothschild

Completed

Genetic Determinant of Foveolar Hypoplasia in Parents of Albinos Children (ALAFOR)

Albinism, Ocular

France
Assistance Publique - Hôpitaux de Paris

Completed

Cord Blood Transplantation in Severe Aplastic Anemia (APCORD)

Hereditary Diseases | Relapse | Acquired Aplastic Anemia | Absence of an HLA Identical Donor

France
Biogen

Completed

A Safety Study of Retinal Gene Therapy for Choroideremia With Administration of BIIB111 (GEMINI)

Choroideremia

United States, Germany, France
Centre Oscar Lambret
CTD-CNO; Laboratoire PRISM

Active, not recruiting

Radical Fimbriectomy for Young BRCA Mutation Carriers (Fimbriectomy)

BRCA1 Mutation | BRCA2 Mutation | Hereditary Breast and Ovarian Cancer

France
Assistance Publique - Hôpitaux de Paris

Completed

Study of Colchicine Resistance in Familial Mediterranean Fever (COLCHI-RESIST)

Colchicine Resistance | Mediterranean Fever

France
Centre Hospitalier Intercommunal Creteil
Bayer

Completed

Aflibercept After Ranibizumab in Exudative Age-related Macular Degeneration (ARI2)

Eye Diseases | Macular Degeneration | Retinal Degeneration | Retinal Diseases | Wet Macular Degeneration

France
Hospices Civils de Lyon

Completed

Efficacy and Safety of a 0.1% Tacrolimus Nasal Ointment as a Treatment for Epistaxis in Hemorrhagic Hereditary Telangiectasia (HHT) (TACRO)

Hemorrhagic Hereditary Telangiectasia (HHT)

France
Columbia University
National Eye Institute (NEI); Centre Hospitalier National d'Ophtalmologie des... and other collaborators

Recruiting

Study of BEST1 Vitelliform Macular Dystrophy

Retinitis Pigmentosa | Best Vitelliform Macular Dystrophy

United States, Germany, France
Ophthalmos Research and Education Institute

Completed

Therapeutic Potential of Omega-3 Fatty Acids Supplementation in Dry Macular Degeneration and Stargardt Disease (MADEOS)

Stargardt Disease 1 | Dry AMD

France, Germany, Italy
University Hospital, Clermont-Ferrand

Recruiting

Prospective Study of Antiplatelet and Anticoagulation Therapy in Hereditary Haemorrhagic Telangiectasia (PROPLACO-Tel)

Hereditary Hemorrhagic Telangiectasia | Rendu Osler Disease

France
University Hospital, Lille

Completed

Adult Outcomes of Children With CAPS (CAPS)

Cryopyrin Associated Periodic Syndrome

France
Assistance Publique - Hôpitaux de Paris

Recruiting

Peripheral Serotonin and Albinism (SEPIAs)

Oculocutaneous Albinism

France
Institut National de la Santé Et de la Recherche...

Recruiting

Eurbio-Alport (RaDiCo Cohort) (RaDiCo Eurbio-Alport) (Eurbio-Alport)

Alport Syndrome

France
Véronique Hentgen

Active, not recruiting

Physical Abilities of Teenagers With Familial Mediterranean Fever (Sport & FMF)

Familial Mediterranean Fever

France
University Hospital, Strasbourg, France

Completed

Bardet-Biedl Syndrome Study: Clinical and Genetic Epidemiology Study in Adults

Bardet-Biedl Syndrome | Orphan Diseases

France
Novartis Pharmaceuticals

Completed

A Study of Canakinumab in Patients With Systemic Juvenile Idiopathic Arthritis or Hereditary Periodic Fevers Who Participated in the CACZ885G2301E1, CACZ885G2306 or CACZ885N2301 Studies

Hereditary Periodic Fevers | Systemic Juvenile Idiopathic Arthritis

France
Hospices Civils de Lyon

Completed

BABH Study: Efficacy and Safety of Bevacizumab on Severe Bleedings Associated With Hemorrhagic Hereditary Telangiectasia (HHT). (BABH)

Telangiectasia, Hereditary Hemorrhagic | Rendu Osler Disease

France
Assistance Publique - Hôpitaux de Paris

Unknown

Quality of Life in Patients With Auto-inflammatory Diseases (MAI-PATIENT)

Hereditary Autoinflammatory Diseases

France
Imagine Institute
RWTH Aachen University; Ruhr University of Bochum; Medical University of Warsaw

Recruiting

Clinical Trial Data Set Re-use With Statistical Methodologies Tailored for Clinical Trials in Rare Diseases (EPISTOPIDEAL)

Epilepsy | Tuberous Sclerosis

France
University Hospital, Montpellier

Unknown

Dermatologic Patterns of Tuberous Sclerosis Patients and Somatic Mutation Relationship

Tuberous Sclerosis Complex

France
University Hospital, Montpellier

Not yet recruiting

Assessment of microRNAs Role in Familial Mediterranean Fever FMF Pathophysiology (miRinFMF)

Familial Mediterranean Fever

France
Assistance Publique - Hôpitaux de Paris

Recruiting

Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) (CILLICORIRCM)

Ciliopathies | Bardet-Biedl Syndrome | Nephronophthisis | Senior-Loken Syndrome | Joubert Syndrome | Jeune Syndrome

France
Assistance Publique - Hôpitaux de Paris
Motion analysis laboratory, Garches; Fondation de Garches

Recruiting

Validation Study of Posturology Platforms for Evaluating Postural Control of Hemiparetic and Neuro-muscular Patients (KPLATES)

Neuromuscular Diseases | Charcot-Marie-Tooth Disease | Hemiparesis

France
Assistance Publique - Hôpitaux de Paris

Completed

Efficacy and Safety of Ustekinumab, a Human Monoclonal Anti-IL-12/IL-23 Antibody, in Patients With Behçet Disease (STELABEC)

Behçet Disease

France
Assistance Publique - Hôpitaux de Paris

Unknown

Musculoskeletal Ultrasound of the Ankles in Erysipelas-like Erythema of Familial Mediterranean Fever (ECHOPERY)

Erysipelas

France
Assistance Publique - Hôpitaux de Paris
French National Referral Center for Neurofibromatoses

Unknown

Modifying Genes in Neurofibromatosis 1 (NFGENMODIF)

Neurofibromatosis 1

France
Rennes University Hospital

Recruiting

Myocardial Effects in Patients With ATTRv With Polyneuropathy Treated With Patisiran or Vutrisiran (MyocardON-TTR)

Transthyretin Amyloidosis | Amyloidosis, Hereditary

France
GenSight Biologics

Completed

Efficacy Study of GS010 for Treatment of Vision Loss From 7 Months to 1 Year From Onset in LHON Due to the ND4 Mutation (REVERSE) (REVERSE)

Optic, Atrophy, Hereditary, Leber

United Kingdom, United States, Germany, Italy, France
Centre Hospitalier National d'Ophtalmologie des...

Recruiting

Bimodal and Coaxial High Resolution Ophtalmic Imaging (AOSLO-OCT)

Stroke | Glaucoma | Hypertension | Diabetes | Retinal Degeneration | Macular Edema | Retinitis Pigmentosa | Retinal Detachment | Vascular Inflammation | Macular Dystrophy | Maculopathy, Age Related

France
Assistance Publique - Hôpitaux de Paris

Completed

Function of the Pigment Epithelium in Patients With Type 1 Neurofibromatosis (NEF-1)

Neurofibromatosis Type 1

France
University Hospital, Toulouse

Unknown

Vision, Attention and Reading in Neurofibromatosis Type 1 (NF1) Children

Neurofibromatosis Type 1

France
ProQR Therapeutics

Active, not recruiting

A Study to Evaluate Efficacy, Safety, Tolerability and Exposure After a Repeat-dose of Sepofarsen (QR-110) in LCA10 (ILLUMINATE) (ILLUMINATE)

Eye Diseases | Neurologic Manifestations | Eye Diseases, Hereditary | Sensation Disorders | Vision Disorders | Blindness | Leber Congenital Amaurosis | Leber Congenital Amaurosis 10 | Retinal Disease | Eye Disorders Congenital

United States, Belgium, Brazil, Canada, France, Germany, Italy, Netherlands, United Kingdom
Centre d'Etude des Cellules Souches
Genethon

Recruiting

Efficacy Study of Daily Administration of VPA in Patients Affected by Wolfram Syndrome (AUDIOWOLF)

Wolfram Syndrome

France, Spain
Hospices Civils de Lyon

Completed

A Diagnostic Test for Familial Mediterranean Fever (DEPIST-FMF)

Familial Mediterranean Fever

France
Genethon

Recruiting

Gene Therapy for Severe Crigler Najjar Syndrome (CareCN)

Crigler-Najjar Syndrome

Italy, France, Netherlands
GenSight Biologics

Completed

Efficacy Study of GS010 for the Treatment of Vision Loss up to 6 Months From Onset in LHON Due to the ND4 Mutation (RESCUE)

Optic, Atrophy, Hereditary, Leber

United Kingdom, United States, France, Germany, Italy
Centre Leon Berard

Recruiting

Evaluation of Percutaneous Cryotherapy in the Treatment of Plexiform Neurofibromas and Unresectable Neurofibromas in Neurofibromatosis Type 1 (CryoNF1)

Neurofibroma | Neurofibroma, Plexiform

France
Assistance Publique - Hôpitaux de Paris
Shire; Zymenex A/S; European Leukodystrophy Association

Completed

Efficacy METAZYM for the Treatment Metachromatic Leukodystrophy Treated With Hematopoietic Stem Cell Transplantation (Azylis)

Metachromatic Leukodystrophy

France
Assistance Publique - Hôpitaux de Paris

Completed

Assessment of the Prevalence of Genes AHI1, NPHP1 and CEP290 in Joubert Syndrome (JSCORS)

Joubert Syndrome | Cerebello-oculo-renal Syndromes

France
University Hospital, Strasbourg, France

Recruiting

Molecular Aspects of Preimplantation Genetic Diagnosis for NF1 (NF1)

Neurofibromatosis Type 1

France
Centre Hospitalier Universitaire de Nice

Unknown

Evaluation of the Analgesic Efficiency of the Transcutaneous Neurostimulation in the Charcot Syndrome Marie Tooth on the Pains of Lower Limbs

CHARCOT MARIE TOOTH DISEASE

France
Pixium Vision SA

Completed

Restoring Vision With the Intelligent Retinal Implant System (IRIS V1)in Patients With Retinal Dystrophy (IRIS-1)

Retinitis Pigmentosa | Choroideremia | Cone Rod Dystrophy

Austria, France, Germany
Second Sight Medical Products
National Eye Institute (NEI)

Completed

Argus® II Retinal Stimulation System Feasibility Protocol

Retinitis Pigmentosa

United States, United Kingdom, France, Mexico, Switzerland
Hospices Civils de Lyon

Completed

ATERO : A Randomised Study With Tranexamic Acid in Epistaxis of Rendu Osler Syndrome

Telangiectasia, Hereditary Hemorrhagic | Osler-Rendu Disease

France
Foundation Fighting Blindness
United States Department of Defense

Completed

A Natural History of the Progression of Stargardt Disease: Retrospective and Prospective Studies (ProgSTAR)

Stargardt Disease

United States, United Kingdom, France, Germany
Ionis Pharmaceuticals, Inc.

Recruiting

Orbit Study: A Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of Intrathecally Administered ION356 in Participants With Pelizaeus Merzbacher Disease (PMD)

Pelizaeus-Merzbacher Disease

France, Netherlands

Clinical Trials on Hereditary Angioedema in France

Sponsors and Collaborators

Medical Conditions

Drug Interventions

CROs by country

CROs in Austria

Conditions

Rare Diseases

Drug Interventions

Dietary Supplements

Sponsor/Collaborators

Locations