Home
Conditions
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.

456 public trials 107 recruiting studies

Refine in advanced search Browse all conditions

Genetic Diseases, Inborn trial results

Completed

Safety and Efficacy of AFQ056 in Adolescent Patients With Fragile X Syndrome

NCT01357239

Conditions: Chromosome Disorders, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +10 more
Locations: Novartis Investigative Site Sacramento, California, United States

Novartis Investigative Site Decatur, Georgia, United States

Novartis Investigative Site Chicago, Illinois, United States

Novartis Investigative Site Boston, Massachusetts, United States

View all 38 locations

View Trial Details

Completed

Durban Diabetes Study:A Study of the Epidemiology of Diabetes Mellitus in Urban South Africans of African Descent (DDS)

NCT02416440

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Diabetes Mellitus, Endocrine System Diseases, +7 more
Locations: University of KwaZulu-Natal Durban, KwaZulu-Natal, South Africa

View Trial Details

Completed

Phase II Randomized Trial:Arginine Butyrate Plus Standard Local Therapy in Patients With Refractory Sickle Cell Ulcers

NCT00004412

Conditions: Anemia, Anemia, Hemolytic, Anemia, Hemolytic, Congenital, +17 more
Locations: University of Illinois College of Medicine Chicago, Illinois, United States

Boston University School of Medicine Boston, Massachusetts, United States

Mount Sinai School of Medicine New York, United States

University of Tennessee, Memphis Cancer Center Memphis, Tennessee, United States

View Trial Details

Completed

Safety and Efficacy of Long-term Somatropin Treatment in Children

NCT01543867

Conditions: Cardiovascular Abnormalities, Cardiovascular Diseases, Chromosome Disorders, +27 more
Locations: Mainz, Germany

View Trial Details

Completed

Study of Uridine Triphosphate (UTP) as an Aerosol Spray for Cystic Fibrosis

NCT00004705

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystic Fibrosis, Digestive System Diseases, +9 more
Locations: Not specified

View Trial Details

Completed

Study of Tauroursodeoxycholic Acid for Hepatobiliary Disease in Cystic Fibrosis

NCT00004441

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystic Fibrosis, Digestive System Diseases, +9 more
Locations: Children's Hospital of Denver Denver, Colorado, United States

Children's Hospital Medical Center - Cincinnati Cincinnati, Ohio, United States

University of Milan Milan, Italy

View Trial Details

Completed

Phase I/II Randomized Study of Hydroxyurea With or Without Clotrimazole in Patients With Sickle Cell Anemia

NCT00004492

Conditions: Anemia, Anemia, Hemolytic, Anemia, Hemolytic, Congenital, +11 more
Locations: University of North Carolina School of Medicine Chapel Hill, North Carolina, United States

View Trial Details

Completed

Phase II Study of the Multichannel Auditory Brain Stem Implant for Deafness Following Surgery for Neurofibromatosis 2

NCT00004437

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cranial Nerve Diseases, Cranial Nerve Neoplasms, +37 more
Locations: Not specified

View Trial Details

Completed

Phase III Randomized Study of the Inhalation of Tobramycin in Patients With Cystic Fibrosis

NCT00004829

Conditions: Bacterial Infection, Bacterial Infections, Bacterial Infections and Mycoses, +15 more
Locations: Not specified

View Trial Details

Completed

Phase III Randomized Study of Interferon Gamma in Children With Severe, Congenital Osteopetrosis

NCT00004402

Conditions: Bone Diseases, Bone Diseases, Developmental, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +9 more
Locations: Not specified

View Trial Details

Genetic Diseases, Inborn

Genetic Diseases, Inborn trial results

Related conditions