- 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 3 of 12.
EudraCT Number: 2016-002417-21 | Sponsor Protocol Number: AK2016-2 | Start Date*: 2016-09-22 | ||||||||||||||||
Sponsor Name:Rigshospitalet | ||||||||||||||||||
Full Title: uPAR-PET/MR in glioma | ||||||||||||||||||
Medical condition: Gliomas | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003138-17 | Sponsor Protocol Number: MO28347 | Start Date*: 2013-06-13 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A double-blind, placebo-controlled, randomised, Phase II study evaluating the efficacy and safety of addition of continuous multiple line bevacizumab treatment to lomustine in second (2nd)-line f... | |||||||||||||
Medical condition: Glioblastoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) LT (Prematurely Ended) IT (Completed) IE (Prematurely Ended) EE (Prematurely Ended) GB (Prematurely Ended) LV (Prematurely Ended) ES (Completed) FI (Prematurely Ended) SE (Completed) PT (Prematurely Ended) BG (Prematurely Ended) GR (Completed) HR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002539-27 | Sponsor Protocol Number: PI2011_843_0001 | Start Date*: 2013-03-05 | |||||||||||
Sponsor Name:CHU Amiens | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002606-54 | Sponsor Protocol Number: 8/2006 | Start Date*: 2006-03-02 | |||||||||||
Sponsor Name:ASL SALERNO 1 | |||||||||||||
Full Title: Investigational use of 5-ALA for fluorescence-guided resection of malignant glioma | |||||||||||||
Medical condition: Glioblastoma multiforme | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002142-37 | Sponsor Protocol Number: SURGE 01-07 | Start Date*: 2007-08-03 | |||||||||||
Sponsor Name:Medizinische Universität Innsbruck | |||||||||||||
Full Title: SUNITINIB (SUTENT, SU11248) in Patients with Recurrent or Progressive Glioblastoma multiforme An Academic Prospective Single-arm Phase II Clinical Trial including Translational Research Studies | |||||||||||||
Medical condition: Glioblastoma multiforme - WHO grade IV First progression/recurrence | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001977-13 | Sponsor Protocol Number: 020221 | Start Date*: 2012-08-01 | |||||||||||
Sponsor Name:Northwest Biotherapeutics Inc | |||||||||||||
Full Title: A Phase III clinical trial evaluating DCVax®-L, autologous dendritic cells (DC) pulsed with tumor lysate antigen for the treatment of glioblastoma multiforme (GBM) | |||||||||||||
Medical condition: Glioblastoma Multiforme | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002801-36 | Sponsor Protocol Number: Can-201 | Start Date*: 2023-03-08 | |||||||||||
Sponsor Name:Cantex Pharmaceuticals Inc. | |||||||||||||
Full Title: A Phase I/II Open Label Study to Assess Safety and Preliminary Evidence of a Therapeutic Effect of Azeliragon Combined with Conventional Concurrent Radiation and Temozolomide in Patients with Newly... | |||||||||||||
Medical condition: Newly diagnosed glioblastoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004418-40 | Sponsor Protocol Number: H9H-MC-JBAL | Start Date*: 2012-02-23 | |||||||||||
Sponsor Name:Lilly S.A, | |||||||||||||
Full Title: A Phase 2 Study of LY2157299 Monohydrate Monotherapy or LY2157299 Monohydrate plus Lomustine Therapy compared to Lomustine Monotherapy in Patients with Recurrent Glioblastoma | |||||||||||||
Medical condition: Glioblastoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) BE (Completed) IT (Completed) PL (Completed) NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021531-13 | Sponsor Protocol Number: UCL/10/0035 | Start Date*: 2011-02-17 | |||||||||||
Sponsor Name:Joint UCLH and UCL Biomedical Research Unit | |||||||||||||
Full Title: Multi-centre, randomised, double-blind phase II study comparing cediranib (AZD2171) plus gefitinib (Iressa, ZD1839) with cediranib plus placebo in subjects with recurrent/progressive glioblastoma (... | |||||||||||||
Medical condition: Glioblastoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004552-15 | Sponsor Protocol Number: NANO-GBM | Start Date*: 2021-03-18 | |||||||||||
Sponsor Name:Centre Jean Perrin | |||||||||||||
Full Title: Phase I/II study of AGuIX nanoparticles with radiotherapy plus concomitant Temozolomide in the treatment of newly diagnosed glioblastoma | |||||||||||||
Medical condition: 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: 2015-002727-25 | Sponsor Protocol Number: UKM12_0017 | Start Date*: 2017-10-20 | |||||||||||
Sponsor Name:Universitätsklinikum Münster | |||||||||||||
Full Title: Controlled clinical trial to evaluate the safety and efficacy of stereotactical photodynamic therapy with 5-aminolevulinic acid (Gliolan®) in recurrent glioblastoma | |||||||||||||
Medical condition: Recurrent glioblastoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023218-30 | Sponsor Protocol Number: 26101 | Start Date*: 2012-12-13 | |||||||||||
Sponsor Name:EORTC | |||||||||||||
Full Title: Phase III trial exploring the combination of bevacizumab and loumustine in patients with first recurrence of a glioblastoma. | |||||||||||||
Medical condition: Recurrent glioblastoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) NL (Completed) AT (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003738-34 | Sponsor Protocol Number: CA209-143 | Start Date*: 2014-06-05 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Randomized Phase 3 Open Label Study of Nivolumab versus Bevacizumab and a Safety Study of Nivolumab or Nivolumab in Combination with Ipilimumab in Adult Subjects with Recurrent Glioblastoma (GBM)... | |||||||||||||
Medical condition: Recurrent glioblastoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) ES (Completed) BE (Completed) DK (Completed) PL (Completed) FR (Completed) NL (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: 2018-004064-62 | Sponsor Protocol Number: SNOXA12C401 | Start Date*: 2019-05-07 | |||||||||||
Sponsor Name:TME Pharma AG | |||||||||||||
Full Title: Single-arm, dose-escalation Phase 1/2 Study of olaptesed pegol (NOX-A12) in combination with irradiation in inoperable or partially resected first-line glioblastoma patients with unmethylated MGMT ... | |||||||||||||
Medical condition: glioblastoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000900-16 | Sponsor Protocol Number: UZB-BN-11-001 | Start Date*: 2011-05-05 | |||||||||||
Sponsor Name:UZ BRUSSEL | |||||||||||||
Full Title: AA randomized phase II clinical trial on the efficacy of axitinib as a monotherapy or in combination with lomustine for the treatment of patients with recurrent glioblastoma | |||||||||||||
Medical condition: • Patients with recurrent central nervous system glioblastoma (histologically confirmed WHO grade IV glioma), at documented recurrence/progression following prior treatment with surgery, radiation ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004058-17 | Sponsor Protocol Number: CV-006 | Start Date*: 2016-02-22 | |||||||||||
Sponsor Name:CytoVac A/S | |||||||||||||
Full Title: An open-label, randomised, Phase II study to investigate the efficacy and safety of ALECSAT treatment as an add-on therapy to radiotherapy and temozolomide in patients with newly diagnosed gliobl... | |||||||||||||
Medical condition: Glioblastoma multiforme | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-004631-92 | Sponsor Protocol Number: WWU20_0041 | Start Date*: 2022-07-26 | |||||||||||
Sponsor Name:Westfälische Wilhelms-Universität Münster, C/o Universitätsklinikum Münster Geschäftsbereich Recht u. Drittmittel | |||||||||||||
Full Title: Phase I/II dose escalation trial of radiodynamic therapy (RDT) with 5-Aminolevulinic acid in patients with first recurrence of glioblastoma | |||||||||||||
Medical condition: recurrence of glioblastoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003722-41 | Sponsor Protocol Number: IOV–GB–1-2014-REGOMA | Start Date*: 2015-04-24 | |||||||||||
Sponsor Name:Istituto Oncologico Veneto – IOV‐IRCCS | |||||||||||||
Full Title: Regorafenib in relapsed glioblastoma. REGOMA study Randomized, controlled open‐label phase II clinical trial | |||||||||||||
Medical condition: Glioblastoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000708-39 | Sponsor Protocol Number: NEU-201901 | Start Date*: 2021-07-16 | |||||||||||
Sponsor Name:Rheinische Friedrich-Wilhelms-Universität Bonn | |||||||||||||
Full Title: Phase I/II trial of meclofenamate in progressive MGMT-methylated glioblastoma under temozolomide second-line therapy | |||||||||||||
Medical condition: Adult patients with IDHwt, MGMT promotor methylated glioblastoma at first relapse | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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