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Genetic Diseases, Inborn

Clinical trial condition

Genetic Diseases, Inborn

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

12,656 public trials 2,147 recruiting studies

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Genetic Diseases, Inborn trial results

Completed

Age of Blood in Sickle Cell Transfusion

NCT03704922

Conditions: Anemia, Anemia, Hemolytic, Anemia, Hemolytic, Congenital, +7 more
Locations: Emory University Atlanta, Georgia, United States

University of North Carolina at Chapel Hill Chapel Hill, North Carolina, United States

Versiti Wisconsin Milwaukee, Wisconsin, United States

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Completed

Clinical Study to Evaluate the Efficacy and Safety of Givinostat in Ambulant Patients With Becker Muscular Dystrophy

NCT03238235

Conditions: Becker Muscular Dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +8 more
Locations: Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico di Milano, UOS Milan, Italy

Leiden University Medical Center LUMC Leiden, Netherlands

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Completed

A Study to Assess Treatment Patterns, Clinical Outcomes, and Healthcare Resource Utilization in Chinese Participants Receiving Upadacitinib for Atopic Dermatitis (AD) Through Chart Review

NCT06503536

Conditions: Atopic Dermatitis (AD), Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dermatitis, +9 more
Locations: Huashan Hospital affiliated to Fudan University /ID# 268259 Shanghai, Shanghai Municipality, China

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Completed

A Study of TAK-660 in Surgical Procedures for People With Hemophilia A.

NCT04941898

Conditions: Blood Coagulation Disorders, Blood Coagulation Disorders, Inherited, Coagulation Protein Disorders, +6 more
Locations: Takeda Selected Site Tokyo, Japan

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Completed

The Role of Red Cell Characteristics, Angiogenesis, Viscosity and Oxygenation in the Pathophysiology of Sickle Cell Related Retinopathy

NCT06396403

Conditions: Anemia, Anemia, Hemolytic, Anemia, Hemolytic, Congenital, +10 more
Locations: Amsterdam UMC Amsterdam, North Holland, Netherlands

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Completed

Treatment of Hereditary Angioedema Prodrome with Recombinant C1-esterase Inhibitor (Ruconest)

NCT06690047

Conditions: Angioedema, Angioedemas, Hereditary, Cardiovascular Diseases, +14 more
Locations: Clinical Research Center of Alabama Birmingham, Alabama, United States

Bernstein Clinical Research Center, LLC Cincinnati, Ohio, United States

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Completed

A Study Evaluating Relative Bioavailability of an Oral Suspension of Abrocitinib and Effect of an Acid Reducing Agent on the Bioavailability of Abrocitinib and Assessing the Taste of Abrocitinib Oral Formulations.

NCT04903093

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dermatitis, Dermatitis, Atopic, +9 more
Locations: New Haven Clinical Research Unit New Haven, Connecticut, United States

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Completed

Mitochondrial Video Assessment Source Material Study

NCT06180421

Conditions: Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +31 more
Locations: Casimir Kingston, Massachusetts, United States

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Completed

A Gene Transfer Therapy Study to Evaluate the Safety of Delandistrogene Moxeparvovec (SRP-9001) in Participants With Duchenne Muscular Dystrophy (DMD)

NCT03375164

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
Locations: Nationwide Children's Hospital Columbus, Ohio, United States

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Completed

A Randomized, Double-blind, Placebo-controlled Study of Delandistrogene Moxeparvovec (SRP-9001) for Duchenne Muscular Dystrophy (DMD)

NCT03769116

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, +7 more
Locations: David Geffen School of Medicine at UCLA Los Angeles, California, United States

Nationwide Children's Hospital Columbus, Ohio, United States

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Genetic Diseases, Inborn

Genetic Diseases, Inborn trial results

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