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Published and searchable clinical trials
NCT05007990
- Conditions
- Batten's Disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Diabetes, +21 more
- Locations
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- National Institutes of Health Clinical Center Bethesda, Maryland, United States
NCT02435940
- Conditions
- Abetalipoproteinemia, Abnormalities, Multiple, Achromatopsia, +100 more
- Locations
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- Foundation Fighting Blindness Columbia, Maryland, United States
Italian NCL Registry: a Registry for NCL as an Integration Tool for Future Therapeutic Strategies
NCT06844877
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +10 more
- Locations
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- IRCCS Fondazione Stella Maris Pisa, Italy
NCT03307304
- Conditions
- Batten Disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +11 more
- Locations
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- National Institutes of Health Clinical Center Bethesda, Maryland, United States
NCT03333200
- Conditions
- ALD, Alpha-Mannosidosis, Batten Disease, +78 more
- Locations
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- UPMC Children's Hospital of Pittsburgh Pittsburgh, Pennsylvania, United States
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +10 more
- Locations
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- University Medical Center Hamburg-Eppendorf (UKE)- Childrens Hospital Hamburg, Germany
- Greater Ormond Street Hospital London, United Kingdom
NCT01873924
- Conditions
- Batten Disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +19 more
- Locations
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- University of Rochester Rochester, New York, United States
NCT02254863
- Conditions
- Adrenal Gland Diseases, Adrenal Insufficiency, Adrenoleukodystrophy, +55 more
- Locations
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- Duke University Medical Center Durham, North Carolina, United States
Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford
NCT01793168
- Conditions
- 1p36 Deletion Syndrome, 3-Methylglutaconic Aciduria, Type V, 4p Deletion Syndrome, Non-Wolf-Hirschhorn Syndrome, +698 more
- Locations
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- Sanford Health Sioux Falls, South Dakota, United States
- Online Patient Enrollment System Sydney, Australia
NYSCF Scientific Discovery Biobank
NCT06203106
- Conditions
- ALS, Adnexal Diseases, Alzheimer Disease, +101 more
- Locations
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- New York Stem Cell Foundation Research Institute New York, United States
NCT04613089
- Conditions
- Batten Disease, CLN1 Disease, CLN10 Disease, +27 more
- Locations
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- University Medical Center Hamburg-Eppendorf Hamburg, Germany
Examining Developmental Outcomes of Children Diagnosed With CLN2 Disease
NCT03862274
- Conditions
- Batten Disease, CLN2, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +11 more
- Locations
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- Nationwide Children's Hospital Columbus, Ohio, United States
Gene Therapy Trial for CLN6 Batten Disease
NCT07582484
- Conditions
- Batten Disease, Batten's Disease, CLN6, +14 more
- Locations
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- University of California, San Diego - Rady Children's La Jolla, California, United States
Safety, Tolerability, and Efficacy of PLX-200 in Patients With CLN3
NCT04637282
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +10 more
- Locations
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Not specified
NCT05642221
- Conditions
- Abnormalities, Multiple, Brain Diseases, Brain Diseases, Metabolic, +33 more
- Locations
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- National Institutes of Health Clinical Center Bethesda, Maryland, United States
NCT02725580
- Conditions
- Ceroid Lipofuscinosis, Neuronal, 6, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +11 more
- Locations
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- Nationwide Children's Hosptial Columbus, Ohio, United States
NCT05174039
- Conditions
- Batten Disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +10 more
- Locations
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- Texas Children Hospital Houston, Texas, United States
Baby Detect : Genomic Newborn Screening
NCT05687474
- Conditions
- 3-Hydroxy 3-Methyl Glutaric Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency, +368 more
- Locations
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- CRMN, Hôpital La Citadelle Liège, Wallonia, Belgium
NCT02678689
- Conditions
- Batten Disease, CLN2 Disease, CLN2 Disorder, +14 more
- Locations
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- Nationwide Children's Hospital Columbus, Ohio, United States
- Universitaetsklinikum Hamburg-Eppendorf Hamburg, Germany
- Children's Hospital Bambino Gesù,IRCCS Rome, Piazza, Italy
- Great Ormond Street Childrens Hospital London, United Kingdom
NCT01586455
- Conditions
- Acute Lymphocytic Leukemia, Acute Myelogenous Leukemia, Adrenal Gland Diseases, +84 more
- Locations
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- Children's Hospital Colorado Denver, Colorado, United States
- New York Medical College Valhalla, New York, United States
- University of Utah Salt Lake City, Utah, United States