Exploring the Activity of RAD001 in Vestibular Schwannomas and Meningiomas
Condition(s):Neurofibromatosis Type 2; Vestibular Schwannomas; MeningiomasLast Updated:May 13, 2020Completed
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Condition(s):Neurofibromatosis Type 2; Vestibular Schwannomas; MeningiomasLast Updated:May 13, 2020Completed
Condition(s):Vestibular Schwannoma; NF2; Neurofibromatosis 2; Acoustic Neuroma; Auditory TumorLast Updated:January 12, 2021Completed
Condition(s):Vestibular Schwannoma; Meningioma; Acoustic Neuroma; Neurofibromatosis Type 2Last Updated:May 11, 2022Terminated
Condition(s):NeurofibromatosisLast Updated:April 4, 2017Completed
Condition(s):Vestibular Schwannoma; Inner Ear Disease; Dizziness; Neurofibromatosis 2; Vestibular DisorderLast Updated:March 16, 2023Enrolling by invitation
Condition(s):Profound Bilateral Deafness Due to; Bilateral Cochlear Aplasia; Bilateral Cochlear Nerve Deficiency; Bilateral Cochlear Ossification Secondary to MeningitisLast Updated:February 15, 2019Unknown status
Condition(s):Bilateral Cochlear Aplasia; Bilateral Cochlear Nerve Deficiency; Bilateral Cochlear Ossification Secondary to MeningitisLast Updated:March 18, 2015Withdrawn
Condition(s):Developmental Cochlear Nerve Deficiency; Acquired Cochlear Nerve Deficiency; Cochlear Aplasia; Post-meningitis Cochlear Ossification; Cochlear MalformationLast Updated:July 5, 2018Completed
Condition(s):Solid Tumors, Adult; Solid Tumor; Mesothelioma (MPM); Epithelioid Hemangioendothelioma (EHE); NF2 Deficient Mesothelioma; Other NF2 Deficient Solid Tumors and Solid Tumors With YAP1/TAZ Fusion Genes; NF2 Deficiency; YAP1 or TAZ Gene FusionsLast Updated:July 10, 2023Recruiting
Condition(s):Acute Leukemia; Adenomatous Polyposis; Adrenocortical Carcinoma; AML; BAP1 Tumor Predisposition Syndrome; Carney Complex; Choroid Plexus Carcinoma; Constitutional Mismatch Repair Deficiency Syndrome; Diamond-Blackfan Anemia; DICER1 Syndrome; Dyskeratosis Congenita; Emberger Syndrome; Familial Acute Myeloid Leukemia; Familial Adenomatous Polyposis; Fanconi Anemia; Familial Cancer; Familial Wilms Tumor; Familial Neuroblastoma; GIST; Hereditary Breast and Ovarian Cancer; Hereditary Paraganglioma-Pheochromocytoma Syndrome; Hodgkin Lymphoma; Juvenile Polyposis; Li-Fraumeni Syndrome; Lynch Syndrome; MDS; Melanoma Syndrome; Multiple Endocrine Neoplasia Type 1; Multiple Endocrine Neoplasia Type 2; Neuroblastoma; Neurofibromatosis Type 1; Neurofibromatosis Type II; Nevoid Basal Cell Carcinoma Syndrome; Non Hodgkin Lymphoma; Noonan Syndrome and Other Rasopathy; Overgrowth Syndromes; Pancreatic Cancer; Peutz-Jeghers Syndrome; Pheochromocytoma/Paraganglioma; PTEN Hamartoma Tumor Syndrome; Retinoblastoma; Rhabdoid Tumor Predisposition Syndrome; Rhabdomyosarcoma; Rothmund-Thomson Syndrome; Tuberous Sclerosis; Von Hippel-Lindau DiseaseLast Updated:May 17, 2023Recruiting
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