Clinical Trials on Aromatic Amino Acid Decarboxylase Deficiency
Total 556 results
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Cycle Pharmaceuticals Ltd.ParexelCompletedHereditary Tyrosinemia, Type ISouth Africa
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Swedish Orphan BiovitrumCompletedEfficacy and Safety of Once Daily Dosing Compared to Twice Daily Dosing of Nitisinone in HT-1 (HT-1)Hereditary Tyrosinemia, Type IBelgium, Denmark, France, Germany, Sweden
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Cytonet GmbH & Co. KGCompletedUrea Cycle DisordersGermany
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Pascoe Pharmazeutische Praeparate GmbHRecruitingChronic Disease | Acute Disease | Vitamin C DeficiencyGermany
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BioMarin PharmaceuticalRecruitingPhenylketonuria (PKU)United States, Germany, Italy
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Nutricia ResearchCompleted
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BioMarin PharmaceuticalActive, not recruiting
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BioMarin PharmaceuticalCompletedPhenylketonuria (PKU)United States, Turkey, Canada, France, Germany, Italy, United Kingdom
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Sutphin DrugsUnknownHereditary Tyrosinemia, Type IIndia
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Charite University, Berlin, GermanyJohannes Gutenberg University MainzCompletedPhenylketonuria | Endothelial Dysfunction
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Washington University School of MedicineUniversity of Missouri-Columbia; Northwestern University; Oregon Health and Science... and other collaboratorsTerminated
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Alexion PharmaceuticalsTerminatedLysosomal Acid Lipase DeficiencyUnited Kingdom, Finland, United States, Italy
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Fresenius KabiNot yet recruitingMalnutrition | Pediatric ALL | Essential Fatty Acid Deficiency | Parenteral Nutrition Associated Liver Disease (PNALD)
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Fondation Ophtalmologique Adolphe de RothschildCompletedAlbinism | Fovea PlanaFrance
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Brendan LeeEunice Kennedy Shriver National Institute of Child Health and Human Development... and other collaboratorsCompletedAmino Acid Metabolism, Inborn Errors | Urea Cycle Disorders | Argininosuccinic AciduriaUnited States
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University of GlasgowCompletedPhenylketonuria (PKU)United Kingdom
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University of WashingtonCompleted
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National Center for Research Resources (NCRR)University of MichiganCompletedTyrosinemia, Type I
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Andrea GropmanEunice Kennedy Shriver National Institute of Child Health and Human Development... and other collaboratorsRecruitingBrain Diseases, Metabolic, Inborn | Amino Acid Metabolism, Inborn Errors | Urea Cycle DisordersUnited States, Canada, Germany, Switzerland
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Tulane University School of MedicineBioMarin PharmaceuticalCompletedPhenylketonuria | Behavior and Behavior Mechanisms | PAH Gene ExpressionUnited States
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Dr. Schär AG / SPACompletedPhenylketonurias | Inborn Errors of Metabolism | Metabolic Disease | PKUUnited Kingdom
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Laboratoires GenévrierCompletedVitiligo | PiebaldismBelgium, France, Italy
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The Hospital for Sick ChildrenBioMarin PharmaceuticalCompletedPhenylketonuria | Mild HyperphenylalaninemiaCanada
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Yassin Abdelghaffar Charity Center for Liver Disease...Society of Friends of Liver Patients in the Arab World (SLPAW)RecruitingHereditary Tyrosinemia, Type IEgypt
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Children's National Research InstituteBoston Children's HospitalRecruitingUrea Cycle DisordersUnited States
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Vitaflo International, LtdCompleted
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University of Missouri-ColumbiaCompleted
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University Hospital, ToursCompletedPhenylketonuriaFrance
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Cycle Pharmaceuticals Ltd.ParexelCompletedHereditary Tyrosinemia, Type ISouth Africa
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University of ZurichCompletedPhenylketonuria (PKU) and HyperphenylalaninemiaSwitzerland
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Swedish Orphan BiovitrumCompletedHereditary Tyrosinemia, Type IGermany, United Kingdom, France
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Cytonet GmbH & Co. KGCRS Clinical Research Services Mannheim GmbHCompleted
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National Center for Research Resources (NCRR)University of TexasCompleted
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Ultragenyx Pharmaceutical IncTerminatedWilson Disease | Ornithine Transcarbamylase Deficiency | Glycogen Storage Disease Type IASpain, United Kingdom, Canada, United States, Brazil
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Dr Adnan AghaRecruitingHypothyroidism | Vitamin C Deficiency | Primary HypothyroidismUnited Arab Emirates
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Travere Therapeutics, Inc.Active, not recruiting
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Horizon Therapeutics, LLCCompletedUrea Cycle DisorderUnited States, Spain, Italy, Switzerland
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SynlogicCompletedHomocystinuriaUnited States
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University of Wisconsin, MadisonTerminated
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Assistance Publique - Hôpitaux de ParisCompleted
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Baylor College of MedicineCompletedUrea Cycle Disorders, InbornUnited States
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University Hospital, Clermont-FerrandUnknown
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Children's Hospital of PhiladelphiaCompletedMaple Syrup Urine DiseaseUnited States
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University Hospital, ToursInstitut National de la Santé Et de la Recherche Médicale, FranceCompletedPKU | HyperphenylalaninemiaFrance
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University of LausanneCompleted
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Children's National Research InstitutePatient-Centered Outcomes Research Institute; Eunice Kennedy Shriver National... and other collaboratorsCompleted
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Promethera TherapeuticsCompletedUrea Cycle DisordersBelgium, Spain, France, Poland
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Kaleido BiosciencesCompletedUrea Cycle DisordersSwitzerland
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National Human Genome Research Institute (NHGRI)CompletedOculocutaneous AlbinismUnited States
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University of Colorado, DenverCompletedHomocystinuriaUnited States