- Trials with a EudraCT protocol (34)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
34 result(s) found for: Langerhans Cell.
Displaying page 1 of 2.
EudraCT Number: 2006-006819-75 | Sponsor Protocol Number: CRAD001C2324 | Start Date*: 2007-10-03 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized double-blind phase III study of RAD001 10 mg/d plus best supportive care versus placebo plus best supportive care in the treatment of patients with advanced pancreatic neuroendocrine t... | |||||||||||||
Medical condition: Pancreatic neuroendocrine tumors (also called pancreatic endocrine tumors or islet cell tumors (ICT)) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) IT (Completed) DE (Completed) ES (Completed) FR (Completed) GR (Completed) BE (Completed) GB (Completed) SK (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005051-20 | Sponsor Protocol Number: HISTIOGEN | Start Date*: Information not available in EudraCT | ||||||||||||||||||||||||||
Sponsor Name:Institute of Mother and Child | ||||||||||||||||||||||||||||
Full Title: Determination Of Molecular Status And Benefit Of Use Fludeoxyglucose (18F-FDG) In PET/CT imagining In Juvenile Patients With Histiocytosis | ||||||||||||||||||||||||||||
Medical condition: histiocytic cell proliferation | ||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: PL (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005053-25 | Sponsor Protocol Number: TRAM | Start Date*: Information not available in EudraCT | ||||||||||||||||||||||||||
Sponsor Name:Institute of Mother and Child | ||||||||||||||||||||||||||||
Full Title: Optimalization Of The Time And Dosage Of Trametinib In BRAF Negative Juvenile Patients With Refractory Histiocytosis Or After Failure Of Vemurafenib Treatment. | ||||||||||||||||||||||||||||
Medical condition: histiocytic cell proliferation | ||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: PL (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005052-37 | Sponsor Protocol Number: BRAVO | Start Date*: 2021-04-01 | ||||||||||||||||||||||||||
Sponsor Name:Institute of Mother and Child | ||||||||||||||||||||||||||||
Full Title: Optymalizacja czasu leczenia i dawkowania wemurafenibu u małoletnich pacjentów z opornymi na konwencjonalną terapię rozrostami z komórek histiocytarnych z obecnością mutacji w genie BRAF. | ||||||||||||||||||||||||||||
Medical condition: histiocytic cell proliferation | ||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: PL (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005806-38 | Sponsor Protocol Number: NO21884 | Start Date*: 2009-10-23 | ||||||||||||||||||||||||||
Sponsor Name:F.Hoffmann-La Roche Ltd. | ||||||||||||||||||||||||||||
Full Title: A multiple ascending dose study to evaluate the safety, tolerability and effect on tumor response of the mTOR inhibitor (RAD001) in combination with the IGF-1R antagonist (R1507) in patients with a... | ||||||||||||||||||||||||||||
Medical condition: PIb: solid malignancy that is metastatic or unresectable PII: C 1: Advanced metastatic renal cell carcinoma C 2: Advanced low- to intermediate grade metastatic or unresectable locoregional pancre... | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-003300-31 | Sponsor Protocol Number: 20159460(c) | Start Date*: 2017-06-13 | |||||||||||
Sponsor Name:Hellenic Society for the Study of Bone Metabolism | |||||||||||||
Full Title: Evaluation of the efficacy of Denosumab in adult patients with Langerhans Cell Histiocytosis (LCH) : a multiple-site, single arm, open label Clinical Trial. | |||||||||||||
Medical condition: Langerhans Cell Histiocytosis (LCH) is a rare disease of unknown etiology with variable clinical course exhibiting both neoplastic and inflammatory features. It is characterized by the accumulatio... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001699-20 | Sponsor Protocol Number: 042011 | Start Date*: 2012-05-18 |
Sponsor Name:St. Anna Kinderkrebsforschung, GmbH | ||
Full Title: LCH-IV International Collaborative Treatment Protocol for Children and Adolescents with LANGERHANS CELL HISTIOCYTOSIS | ||
Medical condition: Langerhans cell histiocytosis | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: AT (Ongoing) BE (Ongoing) NL (Ongoing) DK (Ongoing) NO (Ongoing) IE (Ongoing) IT (Ongoing) SE (Ongoing) CZ (Ongoing) ES (Ongoing) PL (Ongoing) GR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-002388-15 | Sponsor Protocol Number: LCH-III | Start Date*: 2005-03-10 | |||||||||||
Sponsor Name:AZIENDA DI RILIEVO NAZIONALE E DI ALTA SPECIALIZZAZIONE OSPEDALE CIVICO E BENFRATELLI, G.DI CRISTINA E M.ASCOLI | |||||||||||||
Full Title: LCH-III Treatment Protocol of the Third International Study for LANGERHANS CELL HISTIOCYTOSIS | |||||||||||||
Medical condition: Langerhans cell Histiocytosis | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000106-37 | Sponsor Protocol Number: 37.07.-92906 | Start Date*: 2008-08-28 | |||||||||||
Sponsor Name:Klinik für Dermatologie und Allergologie der RUB, St. Josef Hospital | |||||||||||||
Full Title: Studies on the combined treatment using etanercept and ultraviolet B for patients with moderate to severe psoriasis vulgaris | |||||||||||||
Medical condition: Psoriasis vulgaris (Plaque-Typ) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014912-36 | Sponsor Protocol Number: SIM001 | Start Date*: 2009-09-22 |
Sponsor Name:Karolinska Institutet | ||
Full Title: Behandling vid Langerhans cellhistiocytos (LCH) | ||
Medical condition: Langerhans cell histiocytosis | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-002392-40 | Sponsor Protocol Number: LCH-A1 | Start Date*: 2007-10-05 | |||||||||||
Sponsor Name:VU University Medical Center | |||||||||||||
Full Title: LCH-A1, first international study for Langerhans Cell Histiocytosis in adults | |||||||||||||
Medical condition: Langerhans Cell Histiocytosis in adults with single system disease with multifocal bonelesions or with lesions in the craniofacial bones with brain extension or in the vertebral bones with intrasp... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003936-21 | Sponsor Protocol Number: TD-212-2308 | Start Date*: 2015-09-14 | ||||||||||||||||||||||||||
Sponsor Name:Hôpital de Jolimont | ||||||||||||||||||||||||||||
Full Title: A PROSPECTIVE MULTICENTRIC, PROOF OF CONCEPT STUDY TO EVALUATE THE VALUE OF 18-FDG-PET-SCAN ON TUMOUR RESPONSE IN PATIENTS WITH A PROGRESSIVE PANCREATIC ENDOCRINE TUMOUR RECEIVING A COMBINATION THE... | ||||||||||||||||||||||||||||
Medical condition: Progressive well or moderately differentiated neuroendocrine tumour of the pancreas | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: BE (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003568-38 | Sponsor Protocol Number: LCH-IV-G-2016 | Start Date*: 2017-11-14 |
Sponsor Name:Johann Wolfgang Goethe-University Frankfurt am Main | ||
Full Title: German Treatment Optimization Study for Children with De Novo and Relapsed Langerhans cell Histiocytosis (LCH) as Part of the International Study LCH-IV | ||
Medical condition: Langerhans cell Histiocytosis (LCH) | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-023183-40 | Sponsor Protocol Number: CSOM230I2201 | Start Date*: 2011-06-28 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, open-label phase II multicenter study evaluating the efficacy of oral Everolimus alone or in combination with Pasireotide LAR i.m. in advanced progressive pancreatic neuroendocrine tu... | |||||||||||||
Medical condition: advanced progressive pancreatic neuroendocrine tumors (PNET) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) SE (Prematurely Ended) BE (Completed) DK (Prematurely Ended) DE (Completed) HU (Completed) ES (Completed) NL (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000425-45 | Sponsor Protocol Number: | Start Date*: 2012-07-03 | |||||||||||||||||||||
Sponsor Name: | |||||||||||||||||||||||
Full Title: Effects of morning vs evening dosing on the pharmacokinetics and pharmacodynamics of sunitinib. | |||||||||||||||||||||||
Medical condition: Renal Cell Cancer, GIST, pancreatic neuroendocrine tumor | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002312-13 | Sponsor Protocol Number: AK2017-1 | Start Date*: 2017-08-25 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Rigshospitalet | ||||||||||||||||||||||||||||||||||||||
Full Title: PET/CT imaging of uPAR-expression in patients with neuroendocrine tumors using 68Ga-NOTA-AE105 | ||||||||||||||||||||||||||||||||||||||
Medical condition: Patients with neuroendocrine tumors (gastro-entero-pancreatic and bronchopulmonary) | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Ongoing) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-002512-14 | Sponsor Protocol Number: AK2017-2 | Start Date*: 2017-09-04 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Rigshospitalet | ||||||||||||||||||||||||||||||||||||||
Full Title: PET/CT imaging of angiogenesis in patients with neuroendocrine tumors using 68Ga-NODAGA-E[c(RGDyK)]2 | ||||||||||||||||||||||||||||||||||||||
Medical condition: Patients with neuroendocrine tumors (gastro-entero-pancreatic and bronchopulmonary) | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-002196-34 | Sponsor Protocol Number: Neo.Lu.Pa.NET | Start Date*: 2019-11-07 | |||||||||||
Sponsor Name:OSPEDALE SAN RAFFAELE | |||||||||||||
Full Title: A Prospective Phase II Single-Arm Trial on Neoadjuvant Peptide Receptor Radionuclide Therapy with 177Lu-DOTATATE Followed by Surgery for resectable Pancreatic Neuroendocrine Tumors (Neo.Lu.Pa.NET) | |||||||||||||
Medical condition: Resectable pancreatic neuroendocrine tumors | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000888-41 | Sponsor Protocol Number: MetNET1trial | Start Date*: 2014-06-05 | ||||||||||||||||
Sponsor Name:Fondazione IRCCS Istituto Nazionale dei tumori | ||||||||||||||||||
Full Title: Activity and safety of Everolimus in combination with octreotide LAR and Metformin in patients with advanced pancreatic well-differentiated Neuroendocrine Tumors (pWDNETs): a Phase II, open, mono... | ||||||||||||||||||
Medical condition: advanced/ or not resectable well differnciated pancreatic neuroendocrin tumor | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006126-10 | Sponsor Protocol Number: Efalizumab in CTCL | Start Date*: 2008-11-27 |
Sponsor Name:Charité - University Hospital Berlin | ||
Full Title: pilot study to evaluate the efficacy of Efalizumab in patients with cutaneous t-cell lymphoma | ||
Medical condition: The cutaneous T-cell lymphoma (also known as Sézary syndrome) is a common disorder of proliferated cells with characteristics of maligne t-lymphocytes immigrating from the cutaneous blood vessels t... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
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