- Trials with a EudraCT protocol (8)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
8 result(s) found for: Cilengitide.
Displaying page 1 of 1.
EudraCT Number: 2008-000615-15 | Sponsor Protocol Number: EMR200052-013 | Start Date*: 2008-07-14 | |||||||||||
Sponsor Name:Merck KGaA | |||||||||||||
Full Title: Open-label, randomized, controlled Phase I/II study of cilengitide to evaluate the safety and efficacy of the combination of different regimens of cilengitide added to cisplatin, 5-FU, and cetuxima... | |||||||||||||
Medical condition: Recurrent/metastatic squamous cell cancer of the head and neck. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) AT (Completed) DE (Completed) FR (Completed) HU (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004344-78 | Sponsor Protocol Number: EMD121974-011 | Start Date*: 2008-08-28 | |||||||||||
Sponsor Name:Merck KGaA | |||||||||||||
Full Title: Cilengitide in subjects with newly diagnosed glioblastoma multiforme and methylated MGMT gene promoter – a multicenter, open-label, controlled Phase III study, testing cilengitide in combination wi... | |||||||||||||
Medical condition: Newly diagnosed, histologically proven GBM with proven methylated MGMT gene promoter status | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (Completed) AT (Completed) DE (Completed) CZ (Completed) FR (Completed) ES (Prematurely Ended) IT (Prematurely Ended) SK (Completed) HU (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004457-15 | Sponsor Protocol Number: EMD 121974-012 | Start Date*: 2010-08-13 | |||||||||||
Sponsor Name:Merck KGaA | |||||||||||||
Full Title: Cilengitide in subjects with newly diagnosed glioblastoma multiforme and unmethylated MGMT gene promoter - a multicenter, open-label Phase II study, investigating two cilengitide regimens in combin... | |||||||||||||
Medical condition: Newly diagnosed glioblastoma multiforme with unmethylated MGMT gene promoter status | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) IT (Prematurely Ended) FR (Completed) HU (Completed) AT (Completed) ES (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: 2009-016870-33 | Sponsor Protocol Number: CILENT-0902 | Start Date*: 2010-05-20 | |||||||||||
Sponsor Name:Centre Oscar Lambret | |||||||||||||
Full Title: Cilengitide (EMD121974) in combination with irradiation in children and young adults with newly diagnosed diffuse intrinsic pontine glioma : Phase I study | |||||||||||||
Medical condition: Newly diagnosed diffuse intrinsic pontine glioma | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004148-35 | Sponsor Protocol Number: EMR 200037-014 | Start Date*: 2010-04-19 | |||||||||||
Sponsor Name:Merck KGaA | |||||||||||||
Full Title: Cilengitide and cetuximab in combination with platinum-based chemotherapy as first-line treatment for subjects with advanced NSCLC. Open-label, randomized, controlled, multicenter Phase II study in... | |||||||||||||
Medical condition: Advanced non-small cell lung cancer (NSCLC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) BE (Completed) DE (Completed) ES (Completed) FR (Completed) IT (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012324-83 | Sponsor Protocol Number: UZB-BN-09-001 | Start Date*: 2009-07-04 | |||||||||||
Sponsor Name:Prof Bart Neyns | |||||||||||||
Full Title: CeCil: A randomized, non-comparative phase II clinical trial of the effect of radiation therapy plus Temozolomide combined with Cilengitide or Cetuximab on the 1-year overall survival of patients w... | |||||||||||||
Medical condition: Subjects with newly diagnosed glioblastoma, who have met all eligibility criteria for the CENTRIC study (EMD 121974-011 study, EudraCT 2007-004344-78) with the exception of NOT having a tumor with ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011898-33 | Sponsor Protocol Number: HIT-HGG-CilMetro | Start Date*: 2011-11-28 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Martin-Luther-Universität Halle-Wittenberg | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Cilengitide and Metronomic Temozolomide for Relapsed or Refractory High Grade Gliomas or Diffuse Intrinsic Pontine Gliomas in Children and Adolescents - A Phase II Study | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Treatment of relapsed or refractory high grade gliomas and diffuse intrinsic pontine gliomas in paediatric patients ≥ 3 years and < 18 years of age. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
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