- Trials with a EudraCT protocol (235)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
235 result(s) found for: glioblastoma.
Displaying page 7 of 12.
EudraCT Number: 2016-001614-16 | Sponsor Protocol Number: 16TETE04 | Start Date*: 2016-09-22 | |||||||||||
Sponsor Name:INSTITUT CLAUDIUS REGAUD | |||||||||||||
Full Title: A phase I/II multicenter trial evaluating the association of hypofractionated stereotactic radiation therapy and the anti-PD-L1 Durvalumab (Medi4736) for patients with recurrent glioblastoma. | |||||||||||||
Medical condition: Recurrent glioblastoma. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005912-27 | Sponsor Protocol Number: GO27819 | Start Date*: 2012-08-17 | ||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd. | ||||||||||||||||||
Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTICENTER PHASE II STUDY EVALUATING THE EFFICACY AND SAFETY OF ONARTUZUMAB IN COMBINATION WITH BEVACIZUMAB OR ONARTUZUMAB MONOTHERAPY IN PATIEN... | ||||||||||||||||||
Medical condition: Patients with recurrent Glioblastoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) ES (Completed) GB (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-003908-50 | Sponsor Protocol Number: EORTC-1709-BTG | Start Date*: 2018-04-11 | ||||||||||||||||
Sponsor Name:European Organisation for research and Treatment of cancer (EORTC) | ||||||||||||||||||
Full Title: A phase III trial of marizomib in combination with standard temozolomide-based radiochemotherapy versus standard temozolomide-based radiochemotherapy alone in patients with newly diagnosed glioblas... | ||||||||||||||||||
Medical condition: Glioblastoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) GB (GB - no longer in EU/EEA) DK (Completed) DE (Completed) NL (Completed) ES (Completed) AT (Completed) NO (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-002752-27 | Sponsor Protocol Number: NCT-2014-0235/N2M2 | Start Date*: 2018-04-04 | |||||||||||
Sponsor Name:University Hospital Heidelberg | |||||||||||||
Full Title: Umbrella protocol for phase I/IIa trials of molecularly matched targeted therapies plus radiotherapy in patients with newly diagnosed glioblastoma without MGMT promoter methylation: NCT Neuro Maste... | |||||||||||||
Medical condition: Patient with newly diagnosed glioblastoma with unmethylated MGMT promoter | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000699-14 | Sponsor Protocol Number: CINC280X2204 | Start Date*: 2014-02-26 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A Phase Ib/II, open-label, multicenter study of INC280 in combination with buparlisib in adult patients with recurrent glioblastoma | ||
Medical condition: Glioblastoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) ES (Completed) | ||
Trial results: View results |
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: 2016-003841-27 | Sponsor Protocol Number: MDNA-55-05 | Start Date*: 2017-07-19 | |||||||||||
Sponsor Name:Medicenna Therapeutics Inc. | |||||||||||||
Full Title: An Open-Label Non-Randomized, Multi-Center Phase-2 Study of Convection-Enhanced Delivery (CED) of MDNA55 in Adults with Recurrent or Progressive Glioblastoma | |||||||||||||
Medical condition: Glioblastoma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: PL (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: View results |
EudraCT Number: 2004-004849-18 | Sponsor Protocol Number: EMD121974-010 | Start Date*: 2005-07-18 | |||||||||||
Sponsor Name:Merck KGaA | |||||||||||||
Full Title: Cilengitide (EMD121974) and temozolomide with concomitant radiation therapy, followed by cilengitide and temozolomide maintenance therapy in subjects with newly diagnosed glioblastoma multiforme – ... | |||||||||||||
Medical condition: Newly diagnosed Glioblastoma (Astrocytoma, WHO grade IV) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002200-13 | Sponsor Protocol Number: CBGJ398X2201 | Start Date*: 2014-05-09 | |||||||||||
Sponsor Name:NOVARTIS FARMA S.p.A | |||||||||||||
Full Title: A Phase 2, multicenter, open-label study of BGJ398 in patients with recurrent resectable or unresectable Glioblastoma | |||||||||||||
Medical condition: recurrent resectable or unresectable Glioblastoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) NL (Prematurely Ended) ES (Prematurely Ended) BE (Prematurely Ended) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000380-42 | Sponsor Protocol Number: CISTEM08 | Start Date*: 2008-02-21 | ||||||||||||||||
Sponsor Name:ISTITUTO NEUROLOGICO "CARLO BESTA" | ||||||||||||||||||
Full Title: Radiotherapy and chemotherapy with cisplatin and temozolomide for patients affected by primary glioblastoma of new diagnosis | ||||||||||||||||||
Medical condition: Primary GLIOBLASTOMA of first diagnosis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
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: 2016-003468-38 | Sponsor Protocol Number: OLA-TMZ-RTE-01 | Start Date*: 2017-03-17 | |||||||||||
Sponsor Name:Centre François baclesse | |||||||||||||
Full Title: Phase I/IIa study of concomitant radiotherapy with olaparib and temozolomide in unresectable high grade gliomas patients | |||||||||||||
Medical condition: First line treatment of patients with unresectable high-grade gliomas | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000310-15 | Sponsor Protocol Number: HC-MRI-GBM | Start Date*: 2020-03-26 | |||||||||||
Sponsor Name:Christoffer Laustsen | |||||||||||||
Full Title: MRI WITH HYPERPOLARISED PYRUVATE IN GLIOBLASTOMA – A PHASE II STUDY | |||||||||||||
Medical condition: Glioblastoma multiforme | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003417-35 | Sponsor Protocol Number: PARPA-293-002 | Start Date*: 2021-11-10 | |||||||||||
Sponsor Name:Nerviano Medical Sciences S.r.l | |||||||||||||
Full Title: A Phase I/II Combination Study of NMS-03305293 and Temozolomide in Adult Patients with Recurrent Glioblastoma | |||||||||||||
Medical condition: Glioblastoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000742-35 | Sponsor Protocol Number: RTBAIEOP018 | Start Date*: 2021-05-05 | ||||||||||||||||||||||||||
Sponsor Name:ASSOCIAZIONE ITALIANA EMATOLOGIA ONCOLOGIA PEDIATRICA | ||||||||||||||||||||||||||||
Full Title: PROTOCOL FOR THE DIAGNOSIS AND THERAPY OF INTRAOCULAR RETINOBLASTOMA | ||||||||||||||||||||||||||||
Medical condition: Intraocular retinoblastoma | ||||||||||||||||||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001690-16 | Sponsor Protocol Number: BORTEM-17 | Start Date*: 2018-05-29 |
Sponsor Name:Helse Bergen HF | ||
Full Title: Bortezomib sensitization of recurrent glioblastoma with unmethylated MGMT promoter to Temozolomide phase 1B/II study | ||
Medical condition: recurrent or progressed WHO grade IV intracranial glioblastoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003371-34 | Sponsor Protocol Number: CDI-CS-002 | Start Date*: 2015-02-20 | ||||||||||||||||
Sponsor Name:Basilea Pharmaceutica International Ltd. | ||||||||||||||||||
Full Title: An open-label Phase 1/2a study of oral BAL101553 in adult patients with advanced solid tumors and in adult patients with recurrent or progressive glioblastoma or high-grade glioma | ||||||||||||||||||
Medical condition: Advanced or recurrent solid tumors, recurrent or progressive glioblastoma, or high-grade glioma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-005131-74 | Sponsor Protocol Number: pGBM-WBRT/DOX2020 | Start Date*: 2021-02-25 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA MEYER | ||||||||||||||||||
Full Title: Phase II, single-arm, open-label interventional clinical trial to evaluate the role of anthracycline infusion after radiotherapy (RT) in pediatric and young adult patients with glioblastoma (pGBM) | ||||||||||||||||||
Medical condition: First diagnosed glioblastoma | ||||||||||||||||||
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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: 2017-003171-64 | Sponsor Protocol Number: M16-534 | Start Date*: 2018-10-30 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co.KG | |||||||||||||
Full Title: Phase 3b Study for Management of Ocular Side Effects in Subjects with EGFR-Amplified Glioblastoma Receiving Depatuxizumab Mafodotin (ABT-414) | |||||||||||||
Medical condition: EGFR-Amplified Newly diagnosed glioblastoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) NL (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
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