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Genetic Diseases, X-Linked

Clinical trial condition

Genetic Diseases, X-Linked

Explore clinical trials studying Genetic Diseases, X-Linked. Study availability and eligibility vary by location and protocol.

1,243 public trials 227 recruiting studies

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Genetic Diseases, X-Linked trial results

Completed

Safety of 40K Pegylated Recombinant Factor IX in Non-Bleeding Patients With Haemophilia B

NCT00956345

Conditions: Blood Coagulation Disorders, Blood Coagulation Disorders, Inherited, Coagulation Protein Disorders, +9 more
Locations: Novo Nordisk Investigational Site Cincinnati, Ohio, United States

Novo Nordisk Investigational Site Portland, Oregon, United States

Novo Nordisk Investigational Site Richmond, Virginia, United States

Novo Nordisk Investigational Site Copenhagen, Denmark

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Completed

This is a Study to Get More Information About Non Ambulatory Boys & Men With Duchenne Muscular Dystrophy

NCT01098708

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
Locations: Washington University St Louis, Missouri, United States

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Completed

Epidemiological Study on Haemophilia Care and Orthopaedic Status in Developing Countries

NCT01503567

Conditions: Blood Coagulation Disorders, Blood Coagulation Disorders, Inherited, Coagulation Protein Disorders, +13 more
Locations: Novo Nordisk Investigational Site Bangalore, India

Novo Nordisk Investigational Site Casablanca, Morocco

Novo Nordisk Investigational Site Muscat, Oman

Novo Nordisk Investigational Site Sandton, South Africa

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Completed

Impact of Pain on Functional Impairment and Quality of Life in Adults With Hemophilia

NCT01988532

Conditions: Blood Coagulation Disorders, Blood Coagulation Disorders, Inherited, Coagulation Protein Disorders, +13 more
Locations: Novo Nordisk Investigational Site Plainsboro, New Jersey, United States

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Completed

Establishment of Biomarkers for Fabry Disease

NCT01165697

Conditions: Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +19 more
Locations: Eye and Ear Institute Columbus, Ohio, United States

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Completed

Pharmacokinetics of Single Bolus Dose of NovoSeven® in Paediatric and Adult Patients With Haemophilia A or B in a Non- Bleeding State

NCT01562587

Conditions: Blood Coagulation Disorders, Blood Coagulation Disorders, Inherited, Coagulation Protein Disorders, +11 more
Locations: Novo Nordisk Investigational Site Bremen, Germany

Novo Nordisk Investigational Site Frankfurt, Germany

Novo Nordisk Investigational Site Athens, Greece

Novo Nordisk Investigational Site Florence, Italy

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Completed

Exercise Training in Barth Syndrome

NCT01194141

Conditions: Abnormalities, Multiple, Barth Syndrome, Cardiomyopathies, +13 more
Locations: Not specified

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Completed

A PET Brain Imaging Study of mGluR5 in Subjects With Neuropsychiatric Conditions

NCT00870974

Conditions: Alzheimer Disease, Autism Spectrum Disorder, Autistic Spectrum Disorders, +33 more
Locations: Institute for Neurodegenerative Disorders New Haven, Connecticut, United States

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Completed

An Institutional Pilot Study to Investigate Physical Activity Patterns in Boys With Hemophilia

NCT02199717

Conditions: Behavior, Blood Coagulation Disorders, Blood Coagulation Disorders, Inherited, +20 more
Locations: SickKids Toronto, Ontario, Canada

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Completed

Post-marketing Safety Surveillance of NovoSeven® in Patients With Haemophilia and Inhibitors by Means of the UK Haemophilia Database

NCT00853086

Conditions: Blood Coagulation Disorders, Blood Coagulation Disorders, Inherited, Coagulation Protein Disorders, +11 more
Locations: Novo Nordisk Investigational Site Crawley, United Kingdom

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Genetic Diseases, X-Linked

Genetic Diseases, X-Linked trial results

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