- Trials with a EudraCT protocol (84)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
84 result(s) found for: Brain tumours.
Displaying page 1 of 5.
EudraCT Number: 2014-005669-54 | Sponsor Protocol Number: UKM2013-0034 | Start Date*: 2020-06-02 | |||||||||||
Sponsor Name:Universität Münster c/o Universitätsklinikum Münster, Geschäftsbereich Personal und Recht | |||||||||||||
Full Title: Clinical safety study on 5-Aminolevulinic acid (5-ALA) in children and adolescents with brain tumours | |||||||||||||
Medical condition: intra-axial brain tumor (malignant glioma, astrocytoma, malignant ependymoma, AT/RT, Oligodendroglioma, etc.) | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001154-26 | Sponsor Protocol Number: PBTC-020 | Start Date*: 2012-03-09 |
Sponsor Name:Pediatric Brain Tumour Consortium | ||
Full Title: A phase I Clinical Trial of AZD2171 in Children with Recurrent or Progressive Central Nervous System (CNS) Tumours | ||
Medical condition: Recurrent, Progressive, or Refactory Primary CNS Tumours | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: (No results available) |
EudraCT Number: 2004-005247-10 | Sponsor Protocol Number: ITCC-003-Tarceva/Roche MO 18461 | Start Date*: 2005-07-29 |
Sponsor Name:The University Hospitals of Leicester NHS Trust | ||
Full Title: Phase I study of TARCEVA (Erlotinib Hydrochloride, OSI-774) as a single agent in children with refractory and relapsed malignant brain tumours and in combination with irradiation in newly diagnosed... | ||
Medical condition: Refractory and relapsed malignant brain tumours and newly diagnosed brain stem glioma. | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-003227-35 | Sponsor Protocol Number: 755/11 | Start Date*: 2011-10-04 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: 18F-FECh-PET in patients with brain tumors | |||||||||||||
Medical condition: brain tumors | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-005565-40 | Sponsor Protocol Number: OTP-B-Linköping | Start Date*: 2014-09-11 |
Sponsor Name:Department of Biomedical Engineering, Linköping University | ||
Full Title: Optical measurement with 5-ALA during surgical resection of brain tumors in children | ||
Medical condition: Tumour border by means of fluorescenstechnique during surgical resection of brain tumours. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-005786-60 | Sponsor Protocol Number: FET-PET-2010 | Start Date*: Information not available in EudraCT |
Sponsor Name:Charité Universitaetsmedizin Berlin | ||
Full Title: A prospective, multicentre trial on the value of 18F-FET PET in the post-therapeutic evaluation of childhood brain tumours | ||
Medical condition: Children and adolescents with a primary brain tumour after first line therapy | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2008-006288-36 | Sponsor Protocol Number: 1200.24 | Start Date*: 2009-03-16 | |||||||||||||||||||||
Sponsor Name:Boehringer Ingelheim Limited | |||||||||||||||||||||||
Full Title: Phase II open label trial to assess the efficacy and the impact on QTcF of continuous oral BIBW 2992 at a daily dose of 50 mg in patients with relapsed or refractory solid tumours including patient... | |||||||||||||||||||||||
Medical condition: Patients diagnosed with EGFR/HER2-positive solid tumour cancers with and without brain metastases, and patients with recurrent glioblastoma. | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-000630-35 | Sponsor Protocol Number: | Start Date*: 2013-10-07 |
Sponsor Name:Alder Hey Children's NHS Foundation Trust | ||
Full Title: Pilot study on use of Sulphur hexafluoride Microbubbles (SonoVue®) as a Magnetic Resonance Imaging contrast agent in the imaging of brain tumours. | ||
Medical condition: Patients undergoing pre-operative/follow up MRI investigation for a known enhancing brain tumour | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2011-001319-30 | Sponsor Protocol Number: CH/2011/3670 | Start Date*: 2012-04-04 | |||||||||||
Sponsor Name:University Hospitals Bristol NHS Foundation Trust | |||||||||||||
Full Title: A randomized, double-blind, parallel group, placebo-controlled trial of metformin in tuberous sclerosis complex. | |||||||||||||
Medical condition: Tuberous Sclerosis Complex | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001119-30 | Sponsor Protocol Number: 2B3-101-CR-001 | Start Date*: 2011-06-22 | |||||||||||||||||||||||||||||||
Sponsor Name:to-BBB technologies B.V. | |||||||||||||||||||||||||||||||||
Full Title: An open-label, Phase I/IIa, dose escalating study of 2B3-101 in patients with solid tumors and brain metastases or recurrent malignant glioma. | |||||||||||||||||||||||||||||||||
Medical condition: Solid tumors and brain metastases or recurrent malignant glioma, HER2-positive adenocarcinoma of the breast with brain metastases | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: NL (Completed) BE (Completed) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-018072-33 | Sponsor Protocol Number: UKM08_0057 | Start Date*: 2011-08-01 | ||||||||||||||||
Sponsor Name:Universitätsklinikum Münster | ||||||||||||||||||
Full Title: Prospective Trial for the diagnosis and treatment of children, adolescents and young adults with Intracranial Germ Cell Tumours | ||||||||||||||||||
Medical condition: Intracranial Germ Cell tumours of any histology and intracranial site and dissemination | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) SE (Completed) GB (Completed) FR (Completed) AT (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-000589-31 | Sponsor Protocol Number: NEMESIS | Start Date*: 2018-02-02 | ||||||||||||||||
Sponsor Name:SOCIETà CAMPANA DI IMMUNOTERAPIA ONCOLOGICA | ||||||||||||||||||
Full Title: multi stage phase II trial of Nivolumab (an anti –PD-1) in patients with platinum resistant Mismatch Repair deficient germinal cells tumours | ||||||||||||||||||
Medical condition: patients with platinum resistant Mismatch Repair deficient germinal cells tumours | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002123-10 | Sponsor Protocol Number: 1200.120 | Start Date*: 2015-04-18 | ||||||||||||||||||||||||||
Sponsor Name:Boehringer Ingelheim España, S.A. | ||||||||||||||||||||||||||||
Full Title: Phase I open label, dose escalation trial to determine the MTD, safety, PK and efficacy of afatinib monotherapy in children aged 2 years to <18 years with recurrent/refractory neuroectodermal tumou... | ||||||||||||||||||||||||||||
Medical condition: Paediatric patients with recurrent//refractory high grade glioma (HGG), diffuse intrinsic pontine glioma (DIPG), low grade astrocytoma, neuroblastoma, ependymoma, medulloblastoma/primitive neuroect... | ||||||||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: ES (Temporarily Halted) DE (Completed) GB (GB - no longer in EU/EEA) AT (Completed) FR (Completed) DK (Completed) IT (Completed) NL (Completed) IE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-000801-19 | Sponsor Protocol Number: MBMET_MEYER2017 | Start Date*: 2017-11-28 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA MEYER | |||||||||||||
Full Title: An interventional, open-label, Phase II study, to evaluate safety and efficacy of standard and high-dose chemotherapy associated with craniospinal irradiation in patients with metastatic medullobla... | |||||||||||||
Medical condition: Metastatic medulloblastoma and other embryonal tumours | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-006426-43 | Sponsor Protocol Number: IPAX-Linz-01 | Start Date*: 2022-02-16 |
Sponsor Name:Kepler Universitätsklinikum Linz Neuromed Campus | ||
Full Title: An open label, single arm monocentric phase II study to evaluate safety, tolerability, and preliminary efficacy of carrier-added 4-L- [131I]iodophenylalanine (131I-IPA), administered as sequential ... | ||
Medical condition: Previously confirmed histological diagnosis of malignant brain tumours (glioma), with current clinical or imaging evidence for first or second recurrence | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003335-29 | Sponsor Protocol Number: SIOPEATRT01 | Start Date*: 2021-04-15 |
Sponsor Name:German Pediatric Oncology Group, GPOH gGmbH | ||
Full Title: An international prospective umbrella trial for children with atypical teratoid/rhabdoid tumours (ATRT) including A randomized phase III study evaluating the non-inferiority of three courses of hig... | ||
Medical condition: atypical teratoid/rhabdoid tumours (ATRT) | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Ongoing) NO (Trial now transitioned) NL (Trial now transitioned) DK (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2012-000690-23 | Sponsor Protocol Number: ADVL0612;NCI-07-C-0220 | Start Date*: 2012-02-29 | |||||||||||
Sponsor Name:National Institution of Health (NCI) | |||||||||||||
Full Title: A Phase I Study of Sunitinib (SU11248), an Oral Multi-Targeted Tyrosine Kinase Inhibitor, in Children with Refractory Solid Tumors | |||||||||||||
Medical condition: Paediatric solid tumours | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003408-19 | Sponsor Protocol Number: WX/80-003 | Start Date*: 2012-01-25 | |||||||||||
Sponsor Name:WILEX AG | |||||||||||||
Full Title: A Phase I/II, open-label, dose-escalation study to investigate the safety, pharmacokinetics, pharmacodynamics and clinical activity of the MEK inhibitor WX-554 in patients with solid tumours | |||||||||||||
Medical condition: Patients with advanced, metastatic and/or progressive solid tumours for whom there is no effective standard therapy available. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012644-16 | Sponsor Protocol Number: 361/09 | Start Date*: 2009-07-24 | ||||||||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | ||||||||||||||||||
Full Title: PHASE 2 SINGLE- ARM STUDIES OF TEMOZOLOMIDE IN COMBINATION WITH TOPOTECAN IN REFRACTORY AND RELAPSED NEUROBLASTOMA AND OTHER PAEDIATRIC SOLID TUMOURS | ||||||||||||||||||
Medical condition: NEUROBLASTOMA AND OTHER PAEDIATRIC SOLID TUMOURS | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003103-27 | Sponsor Protocol Number: UoL001152 | Start Date*: 2017-01-19 |
Sponsor Name:University of Liverpool | ||
Full Title: A proof of concept phase II study of Buparlisib in HER2 positive breast cancer with brain metastasis following HER2 directed monoclonal antibody therapy | ||
Medical condition: HER2-positive breast cancer with brain metastasis | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
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