Children's National Research Institute
Children's National Research Institute
Washington D.C., District of Columbia, United States3 results ยท Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| A Study of APG-115 in as a Monotherapy or Combination With Pembrolizumab in Patients With Metastatic Melanomas or Advanced Solid Tumors | Neoplasms by Histologic Type, Neoplasms by Site, Neoplasms, Connective and Soft Tissue, Neoplasms, Fibrous Tissue, Neoplasms, Germ Cell and Embryonal, Neoplasms, Nerve Tissue, Skin and Connective Tissue Diseases, Uveal Neoplasms, connective tissue neoplasm, cutaneous melanoma, eye disorder, fibrosarcoma, melanocytic neoplasm, melanoma, mucosal melanoma, neoplasm, nerve sheath neoplasm, nervous system disorder, neuroendocrine neoplasm, neurofibroma, neurofibrosarcoma, neuromuscular disease, ocular cancer, peripheral nervous system disorder, peripheral nervous system neoplasm, primitive neuroectodermal tumor, sarcoma, skin disorder, skin neoplasm, uveal disorder, uveal melanoma | Active, not recruiting | Phase 1 / Phase 2 | 2025-08-07 | NCT03611868 | |
| Research on Optimizing the Use of Technology With Education | Nutritional and Metabolic Diseases, autoimmune disease, diabetes mellitus, endocrine system disorder, glucose metabolism disease, immune system disorder, metabolic disease, type 1 diabetes mellitus | Active, not recruiting | Not applicable | 2025-07-03 | NCT05564481 | |
| Systemic Biomarkers of Brain Injury From Hyperammonemia | Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hypoxia, Hypoxia, Brain, Nutritional and Metabolic Diseases, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, Signs and Symptoms, Respiratory, X-linked disease, arginase deficiency, argininosuccinic aciduria, brain disorder, brain hypoxia - ischemia, brain ischemia, carbamoyl phosphate synthetase I deficiency disease, cardiovascular disorder, carnitine-acylcarnitine translocase deficiency, central nervous system disorder, cerebrovascular disorder, citrullinemia, glutaryl-CoA dehydrogenase deficiency, hereditary disease, hyperammonemia due to N-acetylglutamate synthase deficiency, inborn disorder of amino acid metabolism, inborn errors of metabolism, inborn mitochondrial metabolism disorder, inborn organic aciduria, maple syrup urine disease, medium chain acyl-CoA dehydrogenase deficiency, metabolic disease, mitochondrial trifunctional protein deficiency, nervous system disorder, ornithine carbamoyltransferase deficiency, ornithine translocase deficiency, perinatal asphyxia, urea cycle disorder, vascular disorder, very long chain acyl-CoA dehydrogenase deficiency | Recruiting | Not stated | 2024-02-07 | NCT04602325 |