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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

Biochemical Correction of Severe EB by Allo HSCT and "Off-the-shelf" MSCs

NCT01033552

Conditions: Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Epidermolysis Bullosa, +6 more
Locations: University of Minnesota Masonic Cancer Center and Medical Center Minneapolis, Minnesota, United States

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Completed

Study to Test How Well Patients With Advanced Solid Tumors Respond to Treatment With the Elimusertib in Combination With Pembrolizumab, to Find the Optimal Dose for Patients, How the Drug is Tolerated and the Way the Body Absorbs, Distributes and Discharges the Drug

NCT04095273

Conditions: Advanced Solid Tumors, Ataxia, Ataxia Telangiectasia, +28 more
Locations: Stanford University Palo Alto, California, United States

Yale Cancer Center New Haven, Connecticut, United States

Johns Hopkins Hospital/Health System Baltimore, Maryland, United States

Dana-Farber Cancer Institute Boston, Massachusetts, United States

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Completed

Nexus of Risk: Sexual Assault, Alcohol Use, and Risky Sex Among College Women

NCT05892692

Conditions: Amino Acid Metabolism, Inborn Errors, Behavior, Chemically-Induced Disorders, +15 more
Locations: Logan Hall Albuquerque, New Mexico, United States

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Completed

The Frequency of Superior Cluneal Nerve Entrapment Diagnosed With Ultrasound Guided Nerve Block

NCT05303597

Conditions: Back Pain, Charcot-Marie-Tooth Disease, Congenital Abnormalities, +17 more
Locations: İstanbul Üniversitesi - Cerrahpasa (IUC) Istanbul, Turkey (Türkiye)

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Completed

Jaktinib Hydrochloride Cream For Atopic Dermatitis

NCT04435392

Conditions: Atopic Dermatitis, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dermatitis, +9 more
Locations: The Second Xiangya Hospital of Central South University Changsha, Hunan, China

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Completed

Acute Intermittent Porphyria Related Abnormalities in Cardiovascular System

NCT05882136

Conditions: Arrhythmias, Cardiac, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +17 more
Locations: Institute of Hematology and Transfusion Medicine Warsaw, Poland

National Institute of Cardiology Warsaw, Poland

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Completed

Kineret (Anakinra), in Adult Patients With Colchicine-Resistant Familial Mediterranean Fever

NCT01705756

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Familial Mediterranean Fever, Genetic Diseases, Inborn, +1 more
Locations: Sheba Medical Center Ramat Gan, Israel

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Completed

Low-Density Lipoprotein (LDL) Apheresis Using H.E.L.P. Therapy

NCT00916643

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Familial Hypercholesterolemia, +10 more
Locations: Not specified

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Completed

Physiotherapy and Reaction Time in Hemophilia

NCT06331091

Conditions: Behavior, Blood Coagulation Disorders, Blood Coagulation Disorders, Inherited, +11 more
Locations: Van Yüzüncü Yıl University Van, Turkey (Türkiye)

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Completed

Investigations of the Pathophysiology of Gilles de la Tourette Syndrome. Part 1: Simultaneous PET and 3T MRI

NCT05232955

Conditions: Basal Ganglia Diseases, Brain Diseases, Central Nervous System Diseases, +11 more
Locations: Max Planck Institute for Human Cognitive and Brain Sciences Leipzig, Germany

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Genetic Diseases, Inborn

Genetic Diseases, Inborn trial results

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