- Trials with a EudraCT protocol (16)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
16 result(s) found for: Neurofibroma.
Displaying page 1 of 1.
EudraCT Number: 2018-001846-32 | Sponsor Protocol Number: BUS2018-1 | Start Date*: 2018-09-18 |
Sponsor Name:VO Barnmedicin, Skånes University Hospital | ||
Full Title: Treatment of NF1-related plexiform neurofibroma with trametinib; a single arm, open-label trial with the goals of volumetric partial remission and pain relief | ||
Medical condition: NF1-related plexiform neurofibroma | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
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: 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: 2016-001563-36 | Sponsor Protocol Number: CRAD001MIL04T | Start Date*: 2016-05-12 |
Sponsor Name:Novartis Pharmaceuticals | ||
Full Title: A Phase II Study of RAD001 in the Treatment of Patients With Plexiform Neurofibromas (PN) Associated With Neurofibromatosis Type 1 (NF1) | ||
Medical condition: Plexiform Neurofibroma Associated With Neurofibromatosis Type 1 | ||
Disease: | ||
Population Age: Children, Under 18, Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2009-016922-15 | Sponsor Protocol Number: HSJD-IMANF1 | Start Date*: 2010-02-04 |
Sponsor Name:HOSPITAL SANT JOAN DE DÉU | ||
Full Title: ENSAYO PILOTO CON IMATINIB PARA PACIENTES CON NEUROFIBROMA PLEXIFORME ASOCIADO A LA NEUROFIBROMATOSIS TIPO I. PILOT STUDY WITH IMATINIB FOR PLEXIFORM NEUROFIBROMA IN NEUROFIBROMATOSIS TYPE I PATIENTS | ||
Medical condition: Tratamiento de los neurofibromas plexiformes de alto riesgo no abordables quirúrgicamente en pacientes con neurofibromatosis tipo I | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001317-16 | Sponsor Protocol Number: TRAIN_2019 | Start Date*: 2019-10-30 | ||||||||||||||||
Sponsor Name:ErasmusMC | ||||||||||||||||||
Full Title: The TRAIN study: TRAmetinib In Neurofibromatosis type 1 related symptomatic plexiform neurofibromas | ||||||||||||||||||
Medical condition: Adult patients (age >17 years) with (mosaic) NF1 with inoperable symptomatic plexiform neurofibromas | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-005022-10 | Sponsor Protocol Number: SYN-1748-MAL-0030-I | Start Date*: 2018-02-13 | ||||||||||||||||
Sponsor Name:Technische Universität München, Fakultät für Medizin | ||||||||||||||||||
Full Title: Improvement of synaptic plasticity and cognitive function in RAS pathway disorders | ||||||||||||||||||
Medical condition: Noonan Syndrom and Neurofibromatosis Type 1 | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-002635-41 | Sponsor Protocol Number: 15HI53 | Start Date*: 2018-09-26 | |||||||||||||||||||||
Sponsor Name:Great Ormond Street Hospital | |||||||||||||||||||||||
Full Title: A paediatric phase I/II study of intermittent dosing of the MEK-1 inhibitor selumetinib in children with neurofibromatosis type-1 and inoperable plexiform neurofibroma and/or progressive optic path... | |||||||||||||||||||||||
Medical condition: Neurofibromatosis type 1 associated plexiform neurofibromas Neurofibromatosis type 1 associated progressive or relapsed optic pathway glioma | |||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001572-42 | Sponsor Protocol Number: FCN-159-002 | Start Date*: 2021-12-21 | |||||||||||
Sponsor Name:Shanghai Fosun Pharmaceutical Industrial Development Co.,Ltd. | |||||||||||||
Full Title: A multi-center, open-label, single-arm Phase I dose-escalation and Phase II dose-expansion study to evaluate the safety, tolerability, PK characteristics and anti-tumor activity of FCN-159 in adult... | |||||||||||||
Medical condition: Participants diagnosed with Neurofibromatosis NF1-related plexiform neurofibromas (PN) and symptomatic with requirement of systematic therapy per investigator’s judgment. A PN is defined as a neuro... | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) IT (Ongoing) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002462-41 | Sponsor Protocol Number: TBRU-dS-RAC-PII | Start Date*: 2018-10-29 |
Sponsor Name:CUTISS AG | ||
Full Title: A Phase II, prospective, intra-patient randomized controlled, multicentre study to evaluate the safety and efficacy of an autologous bio-engineered dermo-epidermal skin substitute (EHSG-KF) for the... | ||
Medical condition: Adults and children with full thickness skin defects | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) IT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2009-012088-32 | Sponsor Protocol Number: KKSH-066 | Start Date*: 2010-01-07 | |||||||||||
Sponsor Name:Martin-Luther-Universität Halle-Wittenberg | |||||||||||||
Full Title: Prospektive und randomisierte Multicenter-Studie (Phase III-Studie) zur Verbesserung der Funktion des Nervus facialis und des Nervus vestibulocochlearis nach der Resektion von Akustikusneurinomen d... | |||||||||||||
Medical condition: Akustikusneurinom mit Indikation zur operativen Therapie | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000847-16 | Sponsor Protocol Number: D1532C00057 | Start Date*: 2019-01-29 | |||||||||||
Sponsor Name:National Cancer Institute, Cancer Therapy Evaluation Program | |||||||||||||
Full Title: A Phase 1/2 Study of the Mitogen Activated Protein Kinase Kinase(MEK) 1 Inhibitor Selumetinib (AZD6244, ARRY-142886, Hydrogen Sulfate) in Children With Neurofibromatosis Type 1 (NF1) and Inoperable... | |||||||||||||
Medical condition: Neurofibromatosis type 1 (NF1) | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002604-27 | Sponsor Protocol Number: PCT2017-1 | Start Date*: 2017-10-03 | |||||||||||
Sponsor Name:Department of Clinical Physiology, Nuclear Medicin and PET | |||||||||||||
Full Title: Phase II trial: RGD PET/MRI in sporadic Vestibular Schwannoma | |||||||||||||
Medical condition: Vestibularis Schwannoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002317-19 | Sponsor Protocol Number: KKSH155 | Start Date*: 2020-04-17 | |||||||||||
Sponsor Name:Martin-Luther-Universität Halle-Wittenberg | |||||||||||||
Full Title: Prophylactic nimodipine treatment for hearing preservation after vestibular schwannoma surgery: a randomized multi-center phase III trial | |||||||||||||
Medical condition: Vestibular schwannomas with indication for surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004685-25 | Sponsor Protocol Number: GO29665 | Start Date*: 2016-10-07 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A PHASE I/II, MULTICENTER, OPEN-LABEL, DOSE-ESCALATION STUDY OF THE SAFETY AND PHARMACOKINETICS OF COBIMETINIB IN PEDIATRIC AND YOUNG ADULT PATIENTS WITH PREVIOUSLY TREATED SOLID TUMORS | |||||||||||||
Medical condition: Solid Tumors | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) IE (Completed) DK (Completed) GB (GB - no longer in EU/EEA) DE (Completed) ES (Completed) IT (Completed) FR (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) |
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