- Trials with a EudraCT protocol (115)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
115 result(s) found for: Glioblastoma Multiforme.
Displaying page 3 of 6.
EudraCT Number: 2018-000046-19 | Sponsor Protocol Number: 64616 | Start Date*: 2018-11-26 | ||||||||||||||||||||||||||
Sponsor Name:Radboud University Medical Center | ||||||||||||||||||||||||||||
Full Title: 18F-PSMA PET/CT for visualization of glioblastoma multiforme | ||||||||||||||||||||||||||||
Medical condition: Patients with suspected/detected GBM on T1w-Gd-MRI | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003045-42 | Sponsor Protocol Number: CV-005 | Start Date*: 2014-03-24 | |||||||||||
Sponsor Name:CytoVac A/S | |||||||||||||
Full Title: An Open-labelled, Randomized Phase II Multicentre Study to Investigate Efficacy of Autologous Lymphoid Effector Cells Specific Against Tumour-Cells (ALECSAT) in Patients with Glioblastoma Multiform... | |||||||||||||
Medical condition: The overall purpose of the study is to investigate the efficacy and safety of ALECSAT in GBM patients either with relapse of GBM after first line treatments (followed by reoperation if possible). T... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001363-46 | Sponsor Protocol Number: ML25739 | Start Date*: 2011-08-22 | |||||||||||
Sponsor Name:ROCHE | |||||||||||||
Full Title: RANDOMIZED, NON COMPARATIVE PHASE II TRIAL WITH BEVACIZUMAB AND FOTEMUSTINE IN THE TREATMENT OF RECURRENT GLIOBLASTOMA. | |||||||||||||
Medical condition: Glioblastoma multiforme progressed after a first line treatment with temozolomide and radiotherapy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002685-23 | Sponsor Protocol Number: ICT-107-301 | Start Date*: 2016-08-19 | |||||||||||
Sponsor Name:ImmunoCellular Therapeutics, Ltd. | |||||||||||||
Full Title: A Phase III randomized double-blind, controlled study of ICT-107 with maintenance temozolomide (TMZ) in newly diagnosed glioblastoma following resection and concomitant TMZ chemoradiotherapy. | |||||||||||||
Medical condition: Treatment of newly diagnosed glioblastoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) DE (Prematurely Ended) NL (Ongoing) ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000410-38 | Sponsor Protocol Number: StrateGlio-1802 | Start Date*: 2018-10-17 | ||||||||||||||||
Sponsor Name:Centre Oscar Lambret | ||||||||||||||||||
Full Title: Phase III randomised trial evaluating treatment intensification with temozolomide in adults with a glioblastoma | ||||||||||||||||||
Medical condition: Adults with a de novo glioblastoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005177-29 | Sponsor Protocol Number: EORTC 26052-22053 | Start Date*: 2006-11-10 | |||||||||||
Sponsor Name:EORTC | |||||||||||||
Full Title: Phase III trial comparing conventional adjuvant temozolomide with dose-intensive temozolomide in patients with newly diagnosed glioblastoma | |||||||||||||
Medical condition: Patients with Glioblastoma Multiforme | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) GB (Completed) FR (Completed) LV (Completed) NL (Completed) SI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004968-41 | Sponsor Protocol Number: CPRC 2007-Dr BEAUCHESNE-TEMOFRAC | Start Date*: 2008-02-06 | |||||||||||
Sponsor Name:CHU DE NANCY - DIRECTION DE LA RECHERCHE CLINIQUE ET DE L'INNOVATION | |||||||||||||
Full Title: Essai de phase II testant une association concomitante irradiation cérébrale ultra-fractionnée – témozolomide pour des glioblastomes multiformes inopérables de novo | |||||||||||||
Medical condition: Glioblastomes multiformes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002775-28 | Sponsor Protocol Number: GBM - ANOCEF01 | Start Date*: 2008-10-06 | |||||||||||
Sponsor Name:Centre Georges François Leclerc | |||||||||||||
Full Title: Evaluation de l'association irinotécan/bévacizumab utilisée en néo-adjuvant et en adjuvant d'une radiochimiothérapie avec témozolomide concomitant pour les glioblastomes non résécables. Etude de ph... | |||||||||||||
Medical condition: GLIOBLASTOMES MULTIFORME (GBM) NON RESECABLES | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001533-17 | Sponsor Protocol Number: EORTC26053-22054 | Start Date*: 2007-06-25 | |||||||||||
Sponsor Name:EORTC European Organisation for research and treatment of cancer | |||||||||||||
Full Title: Phase III trial on Concurrent and Adjuvant Temozolomide chemotherapy in non-1p/19q deleted anaplastic glioma. The CATNON Intergroup trial. | |||||||||||||
Medical condition: anaplastic glioma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DE (Completed) FR (Completed) IT (Completed) BE (Completed) ES (Completed) GB (GB - no longer in EU/EEA) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004015-31 | Sponsor Protocol Number: WPD-201 | Start Date*: 2021-09-10 | |||||||||||
Sponsor Name:WPD Pharmaceuticals Sp. z o.o. | |||||||||||||
Full Title: A Multicenter, Open-Label Study of the Efficacy, Safety, and Pharmacokinetics of Intravenously Infused Berubicin in Adult Patients with Recurrent Glioblastoma Multiforme (WHO Grade IV) After Failur... | |||||||||||||
Medical condition: Glioblastoma Multiforme | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003659-40 | Sponsor Protocol Number: CNS-201 | Start Date*: 2022-01-03 | |||||||||||
Sponsor Name:CNS Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Multicenter, Open-Label Study with a Randomized Control Arm of the Efficacy, Safety, and Pharmacokinetics of Intravenously Infused Berubicin in Adult Patients with Recurrent Glioblastoma Multifor... | |||||||||||||
Medical condition: Glioblastoma Multiforme (WHO Grade IV) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) FR (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003129-27 | Sponsor Protocol Number: CBKM120E2102 | Start Date*: 2014-02-25 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: Phase Ib/II multicenter study of buparlisib plus carboplatin or lomustine in patients with recurrent glioblastoma multiforme (GBM) | |||||||||||||
Medical condition: recurrent glioblastoma multiform | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003193-10 | Sponsor Protocol Number: CDKO-125a-002 | Start Date*: 2009-02-24 | ||||||||||||||||
Sponsor Name:Nerviano Medical Sciences S.r.l. | ||||||||||||||||||
Full Title: A phase I/II study of oral PHA-848125AC given daily for 14 consecutive days every 3 weeks in recurrent malignant glioma | ||||||||||||||||||
Medical condition: Phase I Part: Recurrent Malignant Glioma Phase II Part: Recurrent Glioblastoma Multiforme | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-003089-38 | Sponsor Protocol Number: FG001-CT-001 | Start Date*: 2020-09-03 | |||||||||||
Sponsor Name:FluoGuide A/S | |||||||||||||
Full Title: An open-label, dose escalation, single-dose administration, multi-center phase I/II trial of FG001 (an imaging agent), in patients with glioblastoma scheduled for neurosurgery | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022160-13 | Sponsor Protocol Number: H9H-MC-JBAI | Start Date*: 2011-02-21 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: Phase 1b/2a Study Combining LY2157299 with Standard Temozolomide-based Radiochemotherapy in Patients with Newly Diagnosed Malignant Glioma | |||||||||||||
Medical condition: Glioblastoma Multiforme (GBM) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013406-13 | Sponsor Protocol Number: GBM-DC-2009 | Start Date*: 2009-10-07 |
Sponsor Name:Masaryk University | ||
Full Title: First Line Therapy of Glioblastoma Multiforme with Surgical Resection, Irradiation Therapy, Temozolomide and Additional Tumour-Lysate Pulsed Dendritic Cell Vaccination. A Feasibility Phase II Study... | ||
Medical condition: Glioblastoma Multiforme | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-003101-85 | Sponsor Protocol Number: OSAG 101-BSA-05 | Start Date*: 2007-05-14 |
Sponsor Name:Oncoscience AG | ||
Full Title: Phase-III study of standard radiotherapy plus concomitant and adjuvant OSAG 101 (Theraloc®) plus Temozolomide vs. standard radiotherapy plus concomitant and adjuvant Temozolomide in patient with ne... | ||
Medical condition: Glioblastoma multiforme grade IV | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-003911-63 | Sponsor Protocol Number: GERT | Start Date*: 2006-01-12 |
Sponsor Name:University of Heidelberg, Frau I. Gürkan, Kaufmännische Direktorin | ||
Full Title: Combined Radiochemotherapy with Erbitux (Cetuximab) plus Temozolomide in the primary therapy of Glioblastoma Multiforme (GBM) - Phase I/II Trial | ||
Medical condition: Glioblastoma Multiforme (GBM) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003668-30 | Sponsor Protocol Number: KCP-330-004 | Start Date*: 2013-11-12 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Karyopharm Therapeutic, Inc. | ||||||||||||||||||||||||||||||||||||||
Full Title: A Phase 2 Study Evaluating the Efficacy and Safety of Selinexor (KPT-330) in Patients with Recurrent Gliomas | ||||||||||||||||||||||||||||||||||||||
Medical condition: Recurrent glioblastoma or other brain cancer after failure of radiation therapy and temozolomide | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) NL (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-004214-14 | Sponsor Protocol Number: P311-201 | Start Date*: 2016-10-13 | ||||||||||||||||
Sponsor Name:Upsher-Smith Laboratories, Inc. | ||||||||||||||||||
Full Title: A Phase 1/2 Dose-escalation of USL311 as Single Agent and in Combination with Lomustine (CCNU) in Subjects with Advanced Solid Tumors, with Subsequent Single Agent and Combination Phase 2 Cohorts f... | ||||||||||||||||||
Medical condition: Advanced Solid Tumors/Relapsed/Recurrent Glioblastoma Multiforme (GBM) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
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