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Published and searchable clinical trials
NCT07102394
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cutaneous Neurofibroma, Genetic Diseases, Inborn, +20 more
- Locations
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- Johns Hopkins University Baltimore, Maryland, United States
Mirdametinib Monotherapy in Adults With Neurofibromatosis 1 (NF1) and Cutaneous Neurofibromas (cNF).
NCT06159166
- Conditions
- Cutaneous Neurofibroma, Monotherapy, NF1
- Locations
-
- Johns Hopkins Hospital Baltimore, Maryland, United States
Developing Biomarkers of Plexiform Tumor Burden in Patients With Neurofibromatosis-Type 1
NCT05238909
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +18 more
- Locations
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- Ann & Robert H. Lurie Children's Hospital of Chicago Chicago, Illinois, United States
Trial of Selumetinib and Bromodomain Inhibitor With Durvalumab for Sarcomas
NCT05253131
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Fibrosarcoma, Genetic Diseases, Inborn, +23 more
- Locations
-
- The University of Alabama at Birmingham Birmingham, Alabama, United States
NCT02101736
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +18 more
- Locations
-
- Children's Hospital Los Angeles Los Angeles, California, United States
- Children's National Medical Center Washington D.C., District of Columbia, United States
- Lurie Children's Hospital of Chicago Chicago, Illinois, United States
- University of Chicago Chicago, Illinois, United States
NCT00006435
- Conditions
- NF1, Neoplasms, Neoplasms by Histologic Type, +10 more
- Locations
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- National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda, Maryland, United States
NCT00684398
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +16 more
- Locations
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- National Human Genome Research Institute (NHGRI), 9000 Rockville Pike Bethesda, Maryland, United States
NCT01275586
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +18 more
- Locations
-
- Riley Hospital for Children Indianapolis, Indiana, United States
AZD6244 Hydrogen Sulfate for Children With Nervous System Tumors
NCT01362803
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +22 more
- Locations
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- Children's National Medical Center Washington D.C., District of Columbia, United States
- National Institutes of Health Clinical Center Bethesda, Maryland, United States
- Cincinnati Children's Hospital Medical Center Cincinnati, Ohio, United States
- Children's Hospital of Philadelphia Philadelphia, Pennsylvania, United States
Interventions for Reading Disabilities in NF1
NCT02964884
- Conditions
- Communication Disorders, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslexia, +28 more
- Locations
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- Vanderbilt University Nashville, Tennessee, United States