- Trials with a EudraCT protocol (78)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (35)
78 result(s) found for: TRACE.
Displaying page 4 of 4.
EudraCT Number: 2009-016784-11 | Sponsor Protocol Number: IMCLCP12-0917 | Start Date*: 2010-11-05 | |||||||||||
Sponsor Name:ImClone LLC | |||||||||||||
Full Title: An Open-label, Multicenter, Randomized, Phase 2 Study of a Recombinant Human Anti-VEGFR-2 Monoclonal Antibody, IMC-1121B in Combination with Platinum-based Chemotherapy versus Platinum-based Chemot... | |||||||||||||
Medical condition: Non small-cell lung cancer (NSCLC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006715-22 | Sponsor Protocol Number: CP12-0708 | Start Date*: 2008-12-18 | ||||||||||||||||
Sponsor Name:ImClone LLC | ||||||||||||||||||
Full Title: A Phase 2, Open-label Study of IMC-1121B in Combination with Paclitaxel and Carboplatin as First-line Therapy in Patients with Stage IIIB/IV Non-small Cell Lung Cancer | ||||||||||||||||||
Medical condition: Stage IIIB/IV Non-small Cell Lung Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-006778-14 | Sponsor Protocol Number: BT-CL-PGG-LCA0822 | Start Date*: 2009-03-06 | |||||||||||||||||||||
Sponsor Name:Biothera | |||||||||||||||||||||||
Full Title: A Phase 2, Randomized, Efficacy and Safety Study of Imprime PGG® Injection in Combination with Cetuximab and Concomitant Paclitaxel and Carboplatin Therapy in Patients with Previously Untreated Adv... | |||||||||||||||||||||||
Medical condition: Patients with Previously Untreated Advanced (Stage IIIB or IV) Non-Small Cell Lung Cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000304-29 | Sponsor Protocol Number: | Start Date*: 2016-04-05 | |||||||||||||||||||||||||||||||
Sponsor Name:MUST Coordinating Centre, John Hopkins Bloomberg School of Public Health | |||||||||||||||||||||||||||||||||
Full Title: Periocular and Intravitreal Corticosteroids for Uveitic Macular Edema (POINT) Trial | |||||||||||||||||||||||||||||||||
Medical condition: Uveitic macular oedema | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-002282-19 | Sponsor Protocol Number: ΕΑΕ-2018/ΜΜ03 | Start Date*: 2018-09-28 | |||||||||||
Sponsor Name:Hellenic Society of Hematology | |||||||||||||
Full Title: A Phase 2, Multicenter, Open-label, Single-Arm Study to Evaluate the Safety and Efficacy of Daratumumab in Combination with Ixazomib and Dexamethasone as Second Line Therapy in Multiple Myeloma Pat... | |||||||||||||
Medical condition: Relapsed and /or Refractory Multiple Myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003243-37 | Sponsor Protocol Number: | Start Date*: 2017-11-02 | |||||||||||||||||||||||||||||||
Sponsor Name:MUST Coordinating Centre, John Hopkins Bloomberg School of Public Health | |||||||||||||||||||||||||||||||||
Full Title: Macular Edema Ranibizumab v. Intravitreal anti-inflammatory Therapy (MERIT) Trial | |||||||||||||||||||||||||||||||||
Medical condition: Uveitic macular oedema | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GB (Temporarily Halted) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-001413-37 | Sponsor Protocol Number: BELI(E)VE-Trial | Start Date*: 2023-04-24 | |||||||||||
Sponsor Name:University Medical Center Hamburg-Eppendorf | |||||||||||||
Full Title: Combination treatment of Belantamab Mafodotin and Venetoclax in treatment of relapsed and refractory t(11;14) Multiple Myeloma (Phase I/IIa) The BELI(E)VE-Trial | |||||||||||||
Medical condition: relapsed and refractory t(11;14) Multiple Myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-003079-41 | Sponsor Protocol Number: BOLD-100-001 | Start Date*: 2023-01-06 | ||||||||||||||||||||||||||
Sponsor Name:Bold Therapeutics, Inc. (Bold) | ||||||||||||||||||||||||||||
Full Title: A Phase 1b/2a Dose Escalation Study of BOLD-100 in Combination with FOLFOX Chemotherapy in Patients with Advanced Solid Tumours | ||||||||||||||||||||||||||||
Medical condition: Colorectal Cancer Pancreatic Cancer Gastric Cancers Cholangiocarcinoma | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IE (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002502-74 | Sponsor Protocol Number: NEU-01-02-01 | Start Date*: 2012-02-14 | ||||||||||||||||
Sponsor Name:Neurophyxia B.V. | ||||||||||||||||||
Full Title: A multi-centre, randomised, double-blind, placebo-controlled Phase II study to evaluate the efficacy, safety, tolerability, and pharmacokinetics of 2-iminobiotin (2-IB) in neonates with gestational... | ||||||||||||||||||
Medical condition: Perinatal asphyxia | ||||||||||||||||||
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Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: LT (Prematurely Ended) Outside EU/EEA | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-003833-24 | Sponsor Protocol Number: AGMT_HNO_PN | Start Date*: 2016-06-30 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:AGMT – Arbeitsgemeinschaft medikamentöse Tumortherapie gemeinnützige GmbH | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Randomized phase III study: Supplemental parenteral nutrition for patients with locally advanced inoperable tumors of the head and neck, receiving definitive radiotherapy with Cetuximab or Cisplatin | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Locally advanced inoperable tumors of the head and neck under definitive radiotherapy with Cetuximab or Cisplatin | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: AT (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-006780-37 | Sponsor Protocol Number: BT-CL-PGG-LCA0821 | Start Date*: 2009-03-06 | |||||||||||||||||||||
Sponsor Name:Biothera | |||||||||||||||||||||||
Full Title: A Phase 2, Randomized, Efficacy and Safety Study of Imprime PGG® Injection in Combination with Bevacizumab and Concomitant Paclitaxel and Carboplatin Therapy in Patients with Previously Untreated A... | |||||||||||||||||||||||
Medical condition: Patients with with Previously Untreated Advanced (Stage IIIB or IV) Non-Small Cell Lung Cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-006792-42 | Sponsor Protocol Number: EAE120 | Start Date*: 2022-03-09 | |||||||||||
Sponsor Name:Hellenic Society of Hematology (EAE) | |||||||||||||
Full Title: A phase 1/2, dose and schedule evaluation study to investigate the safety and clinical activity of Belantamab Mafodotin administered in combination with Daratumumab, Lenalidomide and Dexamethasone ... | |||||||||||||
Medical condition: newly diagnosed multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001942-39 | Sponsor Protocol Number: EAE128 | Start Date*: 2022-10-24 | |||||||||||
Sponsor Name:Hellenic Society of Hematology (EAE) | |||||||||||||
Full Title: A phase 1/2, dose and schedule evaluation study to investigate the safety and clinical activity of belantamab mafodotin administered in combination with lenalidomide, dexamethasone and nirogacestat... | |||||||||||||
Medical condition: Newly diagnosed patients with multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005826-27 | Sponsor Protocol Number: EAE-2020/MM0107 | Start Date*: 2021-01-26 | |||||||||||
Sponsor Name:Hellenic Society of Hematology (EAE) | |||||||||||||
Full Title: A phase 1/2, dose and schedule evaluation study to investigate the safety and clinical activity of Belantamab Mafodotin administered in combination with Lenalidomide and Dexamethasone in patients w... | |||||||||||||
Medical condition: newly diagnosed multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001941-19 | Sponsor Protocol Number: EAE127 | Start Date*: 2022-10-26 | |||||||||||
Sponsor Name:Hellenic Society of Hematology (EAE) | |||||||||||||
Full Title: A PHASE 1/2, DOSE AND SCHEDULE EVALUATION STUDY TO INVESTIGATE THE SAFETY AND CLINICAL ACTIVITY OF BELANTAMAB MAFODOTIN ADMINISTERED IN COMBINATION WITH POMALIDOMIDE AND DEXAMETHASONE WITH OR WITHO... | |||||||||||||
Medical condition: Relapsed/refractory multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001503-20 | Sponsor Protocol Number: MedOPP150(ATRACTIB) | Start Date*: 2021-07-30 | |||||||||||
Sponsor Name:Medica Scientia Innovation Research (MedSIR) | |||||||||||||
Full Title: PHASE II CLINICAL TRIAL TO EVALUATE THE EFFICACY AND SAFETY OF FIRST LINE ATEZOLIZUMAB IN COMBINATION WITH PACLITAXEL AND BEVACIZUMAB (AVASTIN®) IN PATIENTS WITH ADVANCED OR METASTATIC TRIPLE-NEGAT... | |||||||||||||
Medical condition: Advanced or metastatic triple-negative breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004167-37 | Sponsor Protocol Number: ZX008-1502 | Start Date*: 2016-05-17 | |||||||||||
Sponsor Name:Zogenix International Limited | |||||||||||||
Full Title: A Multicenter, Randomized, Double-blind, Parallel Group, Placebo-controlled Trial of Two Fixed Doses of ZX008 (Fenfluramine Hydrochloride) Oral Solution as an Adjunctive Therapy in Children and You... | |||||||||||||
Medical condition: Dravet's syndrome | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) BE (Completed) NO (Ongoing) DK (Completed) SE (Ongoing) ES (Completed) FR (Ongoing) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002381-18 | Sponsor Protocol Number: VEG107769 | Start Date*: 2007-03-15 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: An Open-Label Extension Study to Assess the Safety and Efficacy of Pazopanib in Subjects with Renal Cell Carcinoma previously enrolled on Protocol VEG105192 | |||||||||||||
Medical condition: Renal Cell Carcinoma | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) GB (Completed) AT (Prematurely Ended) SK (Completed) LT (Completed) EE (Completed) GR (Prematurely Ended) CZ (Completed) IT (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
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