NCT03505853
- Conditions
- Acute Hepatic Porphyria (AHP), Acute Intermittent Porphyria (AIP), Acute Porphyria, +13 more
- Locations
-
- Clinical Trial Site Stockholm, Sweden
Clinical trial condition
Porphyrias
Explore clinical trials studying Porphyrias. Study availability and eligibility vary by location and protocol.
25 public trials
0 recruiting studies
Porphyrias trial results
Completed
A Phase 1 Study of Givosiran (ALN-AS1) in Patients With Acute Intermittent Porphyria (AIP)
NCT02452372
- Conditions
- Acute Intermittent Porphyria, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, +10 more
- Locations
-
- Clinical Trial Site Birmingham, Alabama, United States
- Clinical Trial Site San Francisco, California, United States
- Clinical Trial Site New York, United States
- Clinical Trial Site Galveston, Texas, United States
NCT00004940
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Disease Attributes, +15 more
- Locations
-
Not specified
NCT00004831
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Disease Attributes, +15 more
- Locations
-
Not specified
NCT02082860
- Conditions
- Acute Intermittent Porphyria, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, +10 more
- Locations
-
- 12 Octubre Hospital Madrid, Spain
- Clinica Universidad de Navarra Pamplona, Navarre, Spain
NCT02076763
- Conditions
- Acute Intermittent Porphyria, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, +10 more
- Locations
-
- 12 Octubre Hospital Madrid, Spain
- Clinica Universidad de Navarra Pamplona, Navarre, Spain
NCT00004789
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Disease Attributes, +15 more
- Locations
-
Not specified
NCT00005103
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Disease Attributes, +14 more
- Locations
-
- University of Texas Medical Branch Galveston, Texas, United States
NCT00004330
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Genetic Diseases, Inborn, +8 more
- Locations
-
- University of Texas Medical Branch Galveston, Texas, United States
NCT00004788
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Genetic Diseases, Inborn, +8 more
- Locations
-
Not specified