Natural History and Management of Von Hippel-Lindau (VHL) Associated Pancreatic Neuroendocrine Tumors | ClinicalTrials HQ

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Natural History and Management of Von Hippel-Lindau (VHL) Associated Pancreatic Neuroendocrine Tumors	Abnormalities, Multiple, Ciliopathies, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Digestive System Neoplasms, Neoplasms by Histologic Type, Neoplasms by Site, Neoplasms, Germ Cell and Embryonal, Neoplasms, Multiple Primary, Neoplasms, Nerve Tissue, Neuroectodermal Tumors, Primitive, angiomatosis, cardiovascular disorder, endocrine system disorder, epithelial neoplasm, hereditary disease, hereditary neoplastic syndrome, malignant endocrine neoplasm, multiple endocrine neoplasia, multiple endocrine neoplasia type 1, neoplasm, nervous system disorder, neurocutaneous syndrome, neuroendocrine neoplasm, neuroepithelial neoplasm, pancreas disorder, pancreatic neoplasm, primitive neuroectodermal tumor, vascular disorder, von Hippel-Lindau disease	Recruiting	Phase 2	2026-04-20		NCT04074135

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Organizations	Linked trials
National Cancer Institute (NCI)	3015

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Research sites	City	Country	Linked trials
National Institutes of Health Clinical Center	Bethesda	United States	800