Search clinical trials for: autosomal dominant
Total 449 results
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Centre Hospitalier Universitaire, AmiensActive, not recruiting
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Juan PascualNational Institute of Neurological Disorders and Stroke (NINDS)CompletedGlucose Metabolism Disorders | Epilepsy | Glucose Transporter Type 1 Deficiency Syndrome | Glut1 Deficiency Syndrome 1, Autosomal Recessive | Glucose Transporter Protein Type 1 Deficiency Syndrome | Glucose Transport Defect | GLUT1DS1United States
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Sidney Kimmel Cancer Center at Thomas Jefferson...Bristol-Myers SquibbCompletedLarynx | Lip, Oral Cavity and PharynxUnited States
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Majmaah UniversityCompleted
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Southwest Oncology GroupNational Cancer Institute (NCI)CompletedLymphoma | Nonneoplastic ConditionUnited States
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Rocket Pharmaceuticals Inc.California Institute for Regenerative Medicine (CIRM)TerminatedInfantile Malignant OsteopetrosisUnited States
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Kadmon Corporation, LLCCompletedPolycystic Kidney, Autosomal RecessiveUnited States
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University Hospital, LimogesCompletedScleroderma, SystemicFrance
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Newsom Eye & Laser CenterCompleted
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The Rogosin InstituteWeill Medical College of Cornell UniversityCompleted
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Alliance for Clinical Trials in OncologyNational Cancer Institute (NCI)Completed
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Ramsay Générale de SantéEuropean Clinical Trial Experts NetworkCompleted
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M.D. Anderson Cancer CenterBayerCompleted
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Krystal Biotech, Inc.Active, not recruitingTGM-1 Related Autosomal Recessive Congenital IchthyosisUnited States
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Northwestern UniversityIcahn School of Medicine at Mount SinaiCompletedNetherton Syndrome | Ichthyosis | Lamellar Ichthyosis | Autosomal Recessive Congenital Ichthyosis | Congenital Ichthyosiform Erythroderma | Epidermolytic IchthyosisUnited States
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Phoenicis TherapeuticsTerminatedEpidermolysis Bullosa Dystrophica, Recessive | Epidermolysis Bullosa Dystrophica, DominantUnited States, Spain, France
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British Columbia Cancer AgencyCompleted
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National University Hospital, SingaporeNational University, SingaporeTerminatedCognitive Change | Cerebral HemodynamicsSingapore
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Anna OlczakCompleted
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Cadent TherapeuticsWithdrawnSpinocerebellar Ataxia Type 3 | Spinocerebellar Ataxias | Spinocerebellar Ataxia Type 1 | Spinocerebellar Ataxia Type 2 | Spinocerebellar Ataxia Type 6 | Spinocerebellar Ataxia Type 10 | Spinocerebellar Ataxia Type 7 | Spinocerebellar Ataxia Type 8 | Spinocerebellar Ataxia Type 17 | ARCA1 - Autosomal Recessive...United States
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Inozyme PharmaEngage Health Inc.; GACI GlobalCompletedGeneralized Arterial Calcification in Infancy | Autosomal Recessive Hypophosphatemic Rickets Type 2United States
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Fudan UniversityCompletedMetastatic Breast CancerChina
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National Human Genome Research Institute (NHGRI)Completed
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Children's Mercy Hospital Kansas CityCompletedHypophosphatemic Rickets, X-Linked DominantUnited States
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Lisa HaddadEunice Kennedy Shriver National Institute of Child Health and Human Development...CompletedHIV | ContraceptionUnited States
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Mercy Health OhioTerminatedOpen Fracture | Post-Op Wound InfectionUnited States
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Stanford UniversityNational Cancer Institute (NCI)CompletedLymphomaUnited States
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Azienda Usl di BolognaUnknown
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Jose AguirreCompleted
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Icahn School of Medicine at Mount SinaiNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK); Rare... and other collaboratorsCompletedErythropoietic Protoporphyria | EPP | XLP | X-Linked Protoporphyria | XLPP | X-Linked Dominant Erythropoietic Protoporphyria | XLEPP | XLDPUnited States
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Boehringer IngelheimCompletedPulmonary Disease, Chronic ObstructiveUnited States
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NCIC Clinical Trials GroupEastern Cooperative Oncology GroupCompletedHodgkin LymphomaCanada, United Kingdom, Italy
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Carlos A Acosta-OlivoCompletedRadius Fractures | Bone Fractures | Closed Fractures
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Xiangbei Welman Pharmaceutical Co., LtdCompleted
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Fred Hutchinson Cancer CenterNational Cancer Institute (NCI); National Heart, Lung, and Blood Institute...CompletedSevere Combined Immunodeficiency | Adenosine Deaminase Deficiency | Immune System Disorder | Autosomal Recessive Disorder | Purine-Nucleoside Phosphorylase Deficiency | Severe Combined Immunodeficiency With Absence of T and B Cells | X-Linked Severe Combined ImmunodeficiencyUnited States
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Hospices Civils de LyonCompletedHealthy VolunteersFrance
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University of Colorado, DenverCompletedColor Blindness, AcquiredUnited States
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Universitat de LleidaCompleted
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Wayne State UniversityUnknownAneuploidy | Autosomal Recessive DisorderUnited States
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Abd-Elazeem Abd-Elhameed ElbakryCompletedTympanum; PerforationEgypt
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PfizerCompletedFactor VIII Deficiency, Congenital | Hemophilia A, Congenital | Factor 8 Deficiency, Congenital | Autosomal Hemophilia A | Classic Hemophilia
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Origin BiosciencesCompletedMolybdenum Cofactor Deficiency (MoCD) | Rare Autosomal Recessive Disorder | Deficiency of Activity of Molybdenum-dependent Enzymes (Sulfite Oxidase [SOX], Xanthine Dehydrogenase, and Aldehyde Oxidase)United States
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NYU Langone HealthCompletedAnxiety Disorders | Familial Dysautonomia | Dysthymia | Paroxysmal Hypertension | Autosomal Recessive DiseaseUnited States
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Westfälische Wilhelms-Universität MünsterICON plcUnknownPseudoxanthoma Elasticum | Generalized Arterial Calcification in Infancy | Autosomal Recessive Hypophosphatemic RicketsGermany
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Zealand University HospitalUniversity Hospital Schleswig-HolsteinUnknownHormone-refractory Prostate CancerDenmark, Germany
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Inje UniversityUnknownStrabismus | Intermittent ExotropiaKorea, Republic of
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Montefiore Medical CenterNational Cancer Institute (NCI)Completed
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UCB PharmaCompletedOpen Label Long-Term Safety Study of Certolizumab Pegol (CZP) for Patients With Rheumatoid ArthritisRheumatoid ArthritisUnited States, United Kingdom, Belgium, Germany, Austria, Ireland, Czechia
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H. Lundbeck A/STakedaCompletedDepressive Disorder, MajorFinland, Estonia
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University of UtahCompletedDominantly Inherited Stargardt's Disease (STGD3)United States