NCT03505853
- Conditions
- Acute Hepatic Porphyria (AHP), Acute Intermittent Porphyria (AIP), Acute Porphyria, +13 more
- Locations
-
- Clinical Trial Site Stockholm, Sweden
Clinical trial condition
Porphyrias, Hepatic
Explore clinical trials studying Porphyrias, Hepatic. Study availability and eligibility vary by location and protocol.
47 public trials
4 recruiting studies
Porphyrias, Hepatic trial results
NCT03682731
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Erythropoietic Protoporphyria, +10 more
- Locations
-
- Bispebjerg Hospital Copenhagen, Denmark
- Bispebjerg Hospital Copenhagen NV, Denmark
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
NCT00418795
- Conditions
- Acute Intermittent Porphyria, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, +10 more
- Locations
-
- Univercity Texas Medical Branch Galveston, Texas, United States
Completed
Assessment of Intra-subject Variability in the Bioavailability of Chlorpromazine Hydrochloride
NCT02943213
- Conditions
- Acute Intermittent Porphyria, Adjunct in the Treatment of Tetanus, Anti-Psychotic, +22 more
- Locations
-
- Farmovs Parexel Bloemfontein, Kampuslaan Suid, South Africa
NCT01422915
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Erythropoietic Protoporphyria, +10 more
- Locations
-
- Brigham & Women's Hospital Boston, Massachusetts, 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