NCT01543867
- Conditions
- Cardiovascular Abnormalities, Cardiovascular Diseases, Chromosome Disorders, +27 more
- Locations
-
- Mainz, Germany
Clinical trial condition
Genetic Diseases, Inborn
Explore clinical trials studying Genetic Diseases, Inborn. Study availability and eligibility vary by location and protocol.
449 public trials
107 recruiting studies
Genetic Diseases, Inborn trial results
NCT00004705
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystic Fibrosis, Digestive System Diseases, +9 more
- Locations
-
Not specified
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
NCT00004492
- Conditions
- Anemia, Anemia, Hemolytic, Anemia, Hemolytic, Congenital, +11 more
- Locations
-
- University of North Carolina School of Medicine Chapel Hill, North Carolina, United States
NCT00004437
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cranial Nerve Diseases, Cranial Nerve Neoplasms, +37 more
- Locations
-
Not specified
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
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
NCT00004685
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Genetic Diseases, Inborn, +13 more
- Locations
-
Not specified
Completed
Phase I Randomized Study of CPX for the Treatment of Adult Patients With Mild Cystic Fibrosis
NCT00004428
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystic Fibrosis, Digestive System Diseases, +9 more
- Locations
-
Not specified
NCT00004440
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystic Fibrosis, Digestive System Diseases, +9 more
- Locations
-
Not specified