- ICH GCP
- US Clinical Trials Registry
- Search trials
Clinical Trials on Pyruvate Metabolism, Inborn Errors in United States
Total 2366 results
-
Washington University School of MedicineUniversity of Missouri-Columbia; Northwestern University; Oregon Health and Science... and other collaboratorsTerminated
-
Alexion Pharmaceuticals, Inc.RecruitingHypophosphatasiaItaly, Spain, Israel, Korea, Republic of, Belgium, Germany, United States, China, France, Taiwan, Austria, Japan, India, Australia, Argentina, Poland, Turkey, Brazil, Canada, Thailand, United Kingdom, Slovakia, Czechia
-
Lundquist Institute for Biomedical Innovation at...Swedish Orphan Biovitrum; Cure Sanfilippo FoundationCompleted
-
Mayo ClinicCompleted
-
Mayo ClinicNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK); Oxalosis...Completed
-
BioMarin PharmaceuticalCompleted
-
BioMarin PharmaceuticalCompletedMucopolysaccharidosis VIUnited States
-
BioMarin PharmaceuticalCompletedMucopolysaccharidosis VIUnited States
-
BioMarin PharmaceuticalCompletedMucopolysaccharidosis VIUnited States
-
Amicus TherapeuticsActive, not recruitingBatten Disease | CLN6United States
-
ModernaTX, Inc.RecruitingPropionic AcidemiaUnited States, Canada, United Kingdom
-
Ultragenyx Pharmaceutical IncCompletedGlycogen Storage Disease Type IIIUnited States
-
Horizon Therapeutics, LLCTerminatedUrea Cycle DisorderUnited States
-
Children's National Research InstitutePatient-Centered Outcomes Research Institute; Eunice Kennedy Shriver National... and other collaboratorsCompleted
-
University of NottinghamUniversity College, London; Newcastle University; University of ManchesterUnknownFamilial HypercholesterolemiaUnited Kingdom
-
SynlogicCompletedHealthy Volunteer | Urea Cycle DisorderUnited States
-
Ultragenyx Pharmaceutical IncCompletedOrnithine Transcarbamylase DeficiencyUnited States
-
Baylor College of MedicineCompletedUrea Cycle Disorders | Argininosuccinic Aciduria | Argininosuccinate Lyase DeficiencyUnited States
-
National Center for Research Resources (NCRR)Baylor College of MedicineUnknownAmino Acid Metabolism, Inborn ErrorsUnited States
-
Ultragenyx Pharmaceutical IncTerminatedGlycogen Storage Disease Type IIIUnited States, Spain, Italy
-
PTC TherapeuticsCompletedBH4 Deficiency | HyperphenylalaninemiaUnited States
-
Imperial College London Diabetes CentreUnknownFamilial HypercholesterolemiaUnited Arab Emirates
-
Alexion Pharmaceuticals, Inc.Enrolling by invitationHypophosphatasia (HPP)United States, Italy, Russian Federation, Spain, United Kingdom, Germany, Canada, France, Saudi Arabia, Poland, Australia
-
University of Alabama at BirminghamKaiser Permanente; University of NebraskaCompleted
-
Novartis PharmaceuticalsCompletedIron Overload | Hereditary HemochromatosisUnited States, Germany, Italy, Australia, Canada, France
-
CoA Therapeutics, Inc., a BridgeBio companyTerminatedHealthy Volunteers | Propionic Acidemia | Methylmalonic Acidemia | Organic AcidemiaUnited States
-
University of California, Los AngelesEnrolling by invitationTophaceous GoutUnited States
-
Eva Morava-KoziczNot yet recruitingSLC35A2-CDG - Solute Carrier Family 35 Member A2 Congenital Disorder of GlycosylationUnited States
-
Target PharmaSolutions, Inc.Recordati Rare DiseasesEnrolling by invitationPropionic Acidemia | Methylmalonic Acidemia | HyperammonemiaUnited States
-
La Jolla Pharmaceutical CompanyPRA Health SciencesCompletedHereditary HemochromatosisUnited States, Australia, France, United Kingdom
-
ModernaTX, Inc.RecruitingMethylmalonic AcidemiaUnited States, Spain, Canada, Netherlands, France, Australia, United Kingdom
-
BioMarin PharmaceuticalCompletedPhenylketonuriaUnited States
-
Tulane University School of MedicineBioMarin PharmaceuticalCompletedPhenylketonuria | Behavior and Behavior Mechanisms | PAH Gene ExpressionUnited States
-
Genzyme, a Sanofi CompanyCompletedGaucher DiseaseUnited States
-
University of PennsylvaniaRecruitingLCAT DeficiencyUnited States
-
AstraZenecaCompletedFamilial HypercholesterolemiaUnited States, Spain, Netherlands, Norway, Canada
-
Sanguine BiosciencesTerminatedGlycogen Storage Disease Type IBUnited States
-
Bellicum PharmaceuticalsNo longer availableHurler Syndrome | Inborn Errors of Metabolism | Metachromatic Leukodystrophy | Inherited Metabolic Disorder | Lysosomal Storage DisorderUnited States
-
Children's Hospital of PhiladelphiaTerminatedAlbright Hereditary Osteodystrophy | Pseudohypoparathyroidism Type 1AUnited States
-
59th Medical WingUnited States Air ForceCompleted
-
University of MinnesotaRecruitingGaucher Disease, Type 3United States
-
PfizerWithdrawnType 1 Gaucher DiseaseUnited States
-
National Institute of Neurological Disorders and...CompletedType 2 Gaucher DiseaseUnited States
-
National Institute of Neurological Disorders and...CompletedGaucher DiseaseUnited States
-
National Institute of Neurological Disorders and...Completed
-
Mendel TuchmanUniversity of Colorado, Denver; Children's Hospital of Philadelphia; University... and other collaboratorsTerminatedPropionic Acidemia | Methylmalonic AcidemiaUnited States
-
Cerenis Therapeutics, SATerminatedFamilial HypoalphalipoproteinemiaFrance, United States, Belgium, Canada, Israel, Italy, Netherlands
-
University of Texas Southwestern Medical CenterCompletedInsulin Resistance | Partial Lipodystrophy | Generalized Lipodystrophy | HypoleptinemiaUnited States
-
Amicus TherapeuticsTerminatedType 1 Gaucher DiseaseUnited States, United Kingdom
-
SanofiCompletedGaucher's DiseaseUnited States