- Trials with a EudraCT protocol (57)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4,585)
57 result(s) found for: NF.
Displaying page 1 of 3.
EudraCT Number: 2008-003855-65 | Sponsor Protocol Number: 090701 | Start Date*: 2009-09-21 | ||||||||||||||||
Sponsor Name:Baxter Innovations GmbH | ||||||||||||||||||
Full Title: FEIBA NF: A prospective, open-label, randomized, parallel study to evaluate efficacy and safety of prophylactic versus on-demand treatment in subjects with hemophilia A or B and a high titer inhibitor | ||||||||||||||||||
Medical condition: Hemophilia A or B and a high titer inhibitor | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) BG (Completed) IT (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-015242-30 | Sponsor Protocol Number: 2009-001 | Start Date*: 2009-11-05 |
Sponsor Name:The Walton Centre for Neurology and Neurosurgery NHS Trust | ||
Full Title: An open study to compare the efficacy of immunoglobulin administered subcutaneoulsy (SCIG) with current best practice in patients with Complex Regional Pain Syndrome (CRPS) | ||
Medical condition: Complex Regional Pain Syndrome (CRPS) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2014-001361-28 | Sponsor Protocol Number: GO29365 | Start Date*: 2015-10-07 | |||||||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd. | |||||||||||||||||||||||
Full Title: A Phase Ib/II study evaluating the safety, tolerability and anti-tumor activity of polatuzumab vedotin in combination with rituximab (R) or obinutuzumab (G) plus bendamustine (B) in relapsed or ref... | |||||||||||||||||||||||
Medical condition: Follicular Lymphoma and Diffuse Large B-Cell Lymphoma | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: CZ (Completed) HU (Completed) DE (Completed) GB (GB - no longer in EU/EEA) ES (Ongoing) NL (Completed) FR (Ongoing) IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-001846-15 | Sponsor Protocol Number: CSUC-01/06 | Start Date*: 2006-12-06 |
Sponsor Name:InDex Pharmaceuticals AB | ||
Full Title: A placebo-controlled, randomised, double-blind, single dose proof of concept study of Kappaproct, in steroid resistant or steroid dependent patients with ulcerative colitis of mild to moderate degree | ||
Medical condition: Active ulcerative colitis in steroid refractory or steroid dependent patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2011-001789-16 | Sponsor Protocol Number: PenCTU/2011/CTIMP-005 | Start Date*: 2011-08-26 | |||||||||||
Sponsor Name:Plymouth Hospital NHS Trust | |||||||||||||
Full Title: Investigation of the intra-tumoural concentration and activity of sorafenib in cutaneous schwannomas | |||||||||||||
Medical condition: Neurofibromatosis, type 2 (acoustic neurofibromatosis) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (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: 2020-004835-26 | Sponsor Protocol Number: D169AL00005 | Start Date*: 2021-05-24 | |||||||||||
Sponsor Name:IRCCS-A.O.U. SAN MARTINO-IST | |||||||||||||
Full Title: Single-center, randomized, controlled study to evaluate the effects of a six-month treatment with renal glucose transport inhibitor (SGLT2i) drugs on markers of senescence, inflammation and tubuloi... | |||||||||||||
Medical condition: Chronic Kidney Deseas | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003160-19 | Sponsor Protocol Number: ASL608LIOM01 | Start Date*: 2008-09-07 | |||||||||||
Sponsor Name:G.O.N.O. - GRUPPO ONCOLOGICO NORD OVEST | |||||||||||||
Full Title: CETUXIMAB PLUS IRINOTECAN IN PREVIOUSLY TREATED METASTATIC COLORECTAL CANCER PATIENTS SELECTED ON THE BASIS OF KRAS MUTATION AND EGFR INTRON 1 CA TANDEM REPEATS: PHASE II PROSPECTIVE STUDY AND RETR... | |||||||||||||
Medical condition: colorectal cancer | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002228-42 | Sponsor Protocol Number: P101202 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002520-16 | Sponsor Protocol Number: 626 | Start Date*: 2007-07-06 | |||||||||||
Sponsor Name:Universitätsklinik für klinische Pharmakologie, Medizinische Universität Wien | |||||||||||||
Full Title: The effects of post-conditioning and administration of Vitamin C on intramuscular high energy phosphate levels | |||||||||||||
Medical condition: ischemia reperfusion injury | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-005770-26 | Sponsor Protocol Number: KRONF2 | Start Date*: 2023-10-20 | ||||||||||||||||
Sponsor Name:Medical University of Warsaw | ||||||||||||||||||
Full Title: Phase 2a non-commercial and non-randomized intervention study evaluating the efficacy of crizotinib in the treatment of children with severe type 2 neurofibromatosis, in particular those excluded f... | ||||||||||||||||||
Medical condition: Neurofibromatosis type 2 is a genetically determined primary malignancy resulting from a mutation that disables the function of the cell division control gene and leads to neoplasia such as benign ... | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: PL (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003111-31 | Sponsor Protocol Number: 2007-1-18-20-6 | Start Date*: 2008-07-21 |
Sponsor Name:Charité - Universitaetsmedizin Berlin | ||
Full Title: Influence of postoperative influenza vaccination versus GM-CSF in immune-compromised patients undergoing pancreatic or esophageal resection on the course of immunosuppression and the postoperative ... | ||
Medical condition: Post-operative immunological stimulation in severe immune suppression. The study population is made up of adult, which are able to give their inform consent by their own. The patients are undergoin... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-002231-27 | Sponsor Protocol Number: LOB-LEV-2005-02 | Start Date*: 2006-01-16 | |||||||||||
Sponsor Name:Clínica del Dr. Lobatón | |||||||||||||
Full Title: Estudio prospectivo, in vivo, aleatorizado, controlado, abierto, de fase IV, en grupos paralelos para medir el efecto de los antihistamínicos (levocetirizina 5 mg/día y ebastina 20 mg/día, vía oral... | |||||||||||||
Medical condition: Rinitis alérgica estacional | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001933-16 | Sponsor Protocol Number: 26866138PCR2002 | Start Date*: 2007-03-13 |
Sponsor Name:Christos N. Papandreou | ||
Full Title: "A Phase II, Open-Label study of Velcade(Bortezomib)for patients with Androgen-Independent Prostate Carcinoma who progressed on or after prior chemotherapy" | ||
Medical condition: Treatment of patients with Androgen-Independent Prostate Carcinoma who progressed on or after prior chemotherapy. | ||
Disease: | ||
Population Age: | Gender: Male | |
Trial protocol: GR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-004626-17 | Sponsor Protocol Number: 1101/08 | Start Date*: 2009-03-23 | ||||||||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | ||||||||||||||||||
Full Title: Anti-inflammatory and Anti-platelet effect of Clopidogrel and Aspirin vs Aspirin alone in Symptomatic Polyvascular disease and in patients with multiple recurrent cardiovascular events. | ||||||||||||||||||
Medical condition: Polyvascular disease and in patients with multiple recurrent cardiovascular events. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-004284-27 | Sponsor Protocol Number: CA043-001 | Start Date*: 2022-01-17 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase 1/2 First-in-human Study of BMS-986288 Alone and in Combination with Nivolumab in Advanced Malignant Tumors | |||||||||||||
Medical condition: Advanced solid tumors (squamous cell carcinoma of the head and neck (SCCHN), non-small cell lung cancer (NSCLC), cutaneous melanoma, triple-negative breast cancer (TNBC), renal cell carcinoma (RCC)... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) IT (Trial now transitioned) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000190-28 | Sponsor Protocol Number: IMD-10412002-1 | Start Date*: 2007-03-22 | |||||||||||
Sponsor Name:Institute of Medicinal Molecular Design Inc | |||||||||||||
Full Title: A Single Centre, Double-blind, Randomised Study To Investigate a Single Oral Dose of IMD-1041 in A Nasal Allergen Challenge (NAC) Model | |||||||||||||
Medical condition: It is intended to investigate the potential therapeutic benefit of IKKβ inhibition in man by oral dosing of IMD-1041 in a Nasal Alllergen Challenge. | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019759-23 | Sponsor Protocol Number: PET-CT140410 | Start Date*: 2011-01-12 | |||||||||||
Sponsor Name:Guys' and St. Thomas' NHS Foundation Trust | |||||||||||||
Full Title: Evaluation of [11C]-methionine positron emission computerised tomography (PET CT) in diagnosing neurofibromatosis 1(NF1) - malignant peripheral nerve sheath tumours (MPNST) | |||||||||||||
Medical condition: The diagnosis of malignant peripheral nerve sheath tumours in patients with neurofibromatosis 1 | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019937-85 | Sponsor Protocol Number: dmestatina | Start Date*: 2010-09-16 | |||||||||||
Sponsor Name:Dr. Luis Serra Majem | |||||||||||||
Full Title: Dieta Mediterránea, Ejercicio y Estatinas en el Tratamiento de la Dislipemia | |||||||||||||
Medical condition: Dislipidemia | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003297-13 | Sponsor Protocol Number: D5892N00005 | Start Date*: 2005-12-01 |
Sponsor Name:Imperial College | ||
Full Title: A randomised, double-blind, placebo-controlled, parallel-group study to investigate the effect of Symbicort® and Pulmicort® on HAT and HDAC expression and activity in induced sputum cells obtained ... | ||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
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