- Trials with a EudraCT protocol (15)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
15 result(s) found for: Nuclear organization.
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EudraCT Number: 2019-002716-43 | Sponsor Protocol Number: APJ2015/DOTAMIR-CHEVALIER/VS | Start Date*: 2020-03-23 |
Sponsor Name:CHRU DE NANCY | ||
Full Title: Pilot Study evaluating somatostatin receptor's PET imaging to detect inflammatory phases of myocarditis | ||
Medical condition: infectious myocarditis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005866-39 | Sponsor Protocol Number: I2R-MC-BIDJ | Start Date*: 2012-04-18 | |||||||||||
Sponsor Name:Lilly S.A. | |||||||||||||
Full Title: A Comparison of LY2605541 versus Insulin Glargine Alone or in Combination with Pre study Oral Antihyperglycemic Medications in Patients with Type 2 Diabetes Mellitus Previously Treated with Basal I... | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) GR (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000446-56 | Sponsor Protocol Number: CRT076 | Start Date*: 2016-03-07 | |||||||||||
Sponsor Name:Cristália Produtos Químicos Farmacêuticos Ltda. | |||||||||||||
Full Title: Clinical study to compare recombinant human growth hormone Cristalia (r-hGH Cristalia) versus Genotropin® in prepubertal children with growth deficiency due to deficiency of growth hormone. | |||||||||||||
Medical condition: Growth deficiency due to growth hormone deficiency | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005496-10 | Sponsor Protocol Number: H6Q-MC-S028 | Start Date*: 2009-01-28 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: An Open-label, Randomized, Phase 2 Study of R-CHOP Plus Enzastaurin versus R-CHOP in the First-Line Treatment of Patients with Intermediate and High-Risk Diffuse Large B-Cell Lymphoma | |||||||||||||
Medical condition: First-Line Diffuse Large B-Cell Lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001240-38 | Sponsor Protocol Number: KCP-330-010 | Start Date*: 2014-09-26 | |||||||||||
Sponsor Name:Karyopharm Therapeutics, Inc. | |||||||||||||
Full Title: A Phase 2 Study of the Safety and Anti-tumor Activity of the Oral Selective Inhibitor of Nuclear Export (SINE) Selinexor (KPT-330) in Patients with Refractory and/or Relapsed Richters Transformatio... | |||||||||||||
Medical condition: Primary Refractory and/or Relapsed Richters Transformation (RT) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Prematurely Ended) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000602-18 | Sponsor Protocol Number: BMT-CTN#1301 | Start Date*: 2016-09-26 | |||||||||||
Sponsor Name:National Heart, Lung, and Blood Institute (NHLBI) | |||||||||||||
Full Title: A Randomized, Multi-Center, Phase III Trial of Calcineurin Inhibitor-Free Interventions for Prevention of Graft-versus Host-Disease | |||||||||||||
Medical condition: Acute Leukemia in morphologic complete remission Myelodisplasia with less than 5% blasts in the marrow and no circulating blasts | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004977-23 | Sponsor Protocol Number: DP312804 | Start Date*: 2013-04-25 | |||||||||||
Sponsor Name:SFJ LungCancer, Ltd. | |||||||||||||
Full Title: ARCHER 1050: A RANDOMIZED, OPEN-LABEL, PHASE 3, EFFICACY AND SAFETY STUDY OF DACOMITINIB (PF 00299804) VERSUS GEFITINIB FOR THE FIRST LINE TREATMENT OF LOCALLY ADVANCED OR METASTATIC NON SMALL CELL... | |||||||||||||
Medical condition: Non-Small Cell Lung Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) IT (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001261-40 | Sponsor Protocol Number: I2R-MC-BIAN | Start Date*: 2012-03-05 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: Protocol I2R-MC-BIAN (a) Study: The Impact of LY2605541 versus Insulin Glargine for Patients with Type 1 Diabetes Mellitus Treated with Preprandial Insulin Lispro: an Open-Label, Randomized, 78 w... | |||||||||||||
Medical condition: Type 1 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002315-17 | Sponsor Protocol Number: MGL-3196-06 | Start Date*: 2017-01-12 | |||||||||||
Sponsor Name:Madrigal Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 2, Multi-Center, Double-Blind, Randomized, Placebo-controlled Study of MGL-3196 in Patients with Heterozygous Familial Hypercholesterolemia | |||||||||||||
Medical condition: Heterozygous Familial Hypercholesterolemia (HeFH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) DK (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004136-36 | Sponsor Protocol Number: 1002-040 | Start Date*: 2016-06-14 | ||||||||||||||||||||||||||
Sponsor Name:Esperion Therapeutics, Inc. | ||||||||||||||||||||||||||||
Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTI-CENTER LONG-TERM SAFETY AND TOLERABILITY STUDY OF ETC-1002 IN PATIENTS WITH HYPERLIPIDEMIA AT HIGH CARDIOVASCULAR RISK WHO ARE NOT ADEQUATELY C... | ||||||||||||||||||||||||||||
Medical condition: Treatment of high cardiovascular risk patients (heterozygous familial hypercholesterolemia [HeFH] and atherosclerotic cardiovascular diseases [ASCVD]) with hyperlipidemia | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: NL (Completed) GB (Completed) DE (Completed) PL (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-001937-40 | Sponsor Protocol Number: EORTC 16032-18031 | Start Date*: 2005-05-19 | |||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||
Full Title: Randomized, open phase II study of immunization with the recombinant MAGE-3 protein combined with adjuvant AS02B or AS15 in patients with unresectable and progressive metastatic cutaneous melanoma | |||||||||||||
Medical condition: Unresectable and progressive metastatic cutaneous melanoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001508-12 | Sponsor Protocol Number: CVAY736X2208 | Start Date*: 2018-11-02 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A placebo-controlled, patient and investigator blinded, randomized parallel cohort study to assess pharmacodynamics, pharmacokinetics, safety, tolerability and preliminary clinical efficacy of VA... | |||||||||||||
Medical condition: Systemic lupus erythematosus (SLE) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) ES (Completed) FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003700-44 | Sponsor Protocol Number: BGB-A317-207 | Start Date*: 2018-06-21 | |||||||||||
Sponsor Name:BeiGene, Ltd. c/o BeiGene USA, Inc. | |||||||||||||
Full Title: A Phase 2, Open-Label Study of BGB-A317 in Patients with Relapsed or Refractory Mature T- and NK-cell Neoplasms | |||||||||||||
Medical condition: Relapsed or Refractory Mature T- and NK-cell Neoplasms | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002919-18 | Sponsor Protocol Number: AC220-A-U202 | Start Date*: Information not available in EudraCT | |||||||||||||||||||||
Sponsor Name:Daiichi Sankyo, Inc. | |||||||||||||||||||||||
Full Title: A Phase 1/2, Multicenter, Dose-Escalating Study To Evaluate the Safety, Pharmacokinetics, Pharmacodynamics, and Efficacy Of Quizartinib Administered in Combination with Re-Induction Chemotherapy, a... | |||||||||||||||||||||||
Medical condition: Relapsed or Refractory acute myeloid leukemia (AML) in subjects aged ≥1 month to ≤21 years with FMS-like tyrosine kinase 3 (FLT3)-internal tandem duplication (ITD) mutations following failure of fr... | |||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IE (Prematurely Ended) FR (Trial now transitioned) DK (Trial now transitioned) ES (Ongoing) BE (Trial now transitioned) SE (Trial now transitioned) NL (Trial now transitioned) GB (GB - no longer in EU/EEA) IT (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003486-26 | Sponsor Protocol Number: 1002-047 | Start Date*: 2017-05-24 | ||||||||||||||||
Sponsor Name:Esperion Therapeutics Inc., | ||||||||||||||||||
Full Title: A Long-term, Randomized, Double-blind, Placebo-controlled, Multicenter Study to Evaluate the Efficacy of Bempedoic Acid (ETC-1002) in Patients with Hyperlipidemia at High Cardiovascular Risk Not Ad... | ||||||||||||||||||
Medical condition: Patients with Hyperlipidemia at High Cardiovascular Risk Not Adequately Controlled by Their Lipid-Modifying Therapy | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) GB (Completed) | ||||||||||||||||||
Trial results: View results |
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