- Trials with a EudraCT protocol (39,276)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
39,276 result(s) found for: $1.
Displaying page 1,596 of 1,964.
EudraCT Number: 2009-017686-34 | Sponsor Protocol Number: URO-VAR-2010-01 | Start Date*: 2010-05-26 | |||||||||||
Sponsor Name:UROLOGY ASSOCIATES S.L. | |||||||||||||
Full Title: ENSAYO CLÍNICO, FASE IIIb, MULTICÉNTRICO, DOBLE CIEGO, PARA EVALUAR LA EFICACIA DE VARDENAFILO BUCODISPERSABLE vs PLACEBO, EN PACIENTES CON DISFUNCIÓN ERÉCTIL MAS COMORBILIDAD Y EL IMPACTO EN LA CA... | |||||||||||||
Medical condition: Pacientes con disfunción eréctil que presenten dislipemia, hipertensión, diabetes y/o obesidad. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012718-35 | Sponsor Protocol Number: Loulla001 | Start Date*: 2010-05-05 | |||||||||||
Sponsor Name:Only For Children Pharmaceuticals | |||||||||||||
Full Title: An open-label, randomised crossover pharmacokinetic, palatability and safety study to assess the bioavailability of a new 6MP oral liquid formulation by comparison to a currently registered 6MP 50 ... | |||||||||||||
Medical condition: Acute Lymphoblastic Leukemia | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) DE (Ongoing) DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018979-16 | Sponsor Protocol Number: SAXA24011980GLIPTIN | Start Date*: 2010-08-23 | |||||||||||
Sponsor Name:University Hospital Erlangen | |||||||||||||
Full Title: EFFECTS OF SAXAGLITPIN ON ENDOTHELIAL FUNCTION IN PATIENTS WITH TYPE 2 DIABETES | |||||||||||||
Medical condition: diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020098-18 | Sponsor Protocol Number: 2010-605 | Start Date*: 2010-09-09 | |||||||||||
Sponsor Name:HOSPICES CIVILS DE LYON | |||||||||||||
Full Title: CrYSTobs A cohort of patients with cystinosis : compliance to cysteamine and neurological complications An auxiliary study to Raptor RP103 03 and RP103 04 | |||||||||||||
Medical condition: nephropatic cystinosis | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016588-12 | Sponsor Protocol Number: RV-HL-GOTEL-440 | Start Date*: 2010-09-29 | |||||||||||
Sponsor Name:Grupo Oncológico para el Tratamiento y Estudio de los Linfomas (GOTEL) | |||||||||||||
Full Title: ENSAYO FASE II PARA VALORAR LA COMBINACIÓN DE LENALIDOMIDA CON DOSIS METRONÓMICAS DE CICLOFOSFAMIDA EN PACIENTES CON LINFOMA DE HODGKIN CLÁSICO REFRACTARIO O EN RECAÍDA | |||||||||||||
Medical condition: Linfoma de Hodgkin clásico recidivado o refractario. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021872-27 | Sponsor Protocol Number: ICO-20431 | Start Date*: 2010-12-27 | |||||||||||
Sponsor Name:Institut Català dOncologia (ICO) | |||||||||||||
Full Title: Estudio de fase II de tratamiento neoadyuvante con gemcitabina, Tarceva® y oxaliplatino, seguido de quimiorradioterapia con Tarceva® y gemcitabina en pacientes con adenocarcinoma pancreático de re... | |||||||||||||
Medical condition: ADENOCARCINOMA DE PANCREAS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022826-34 | Sponsor Protocol Number: 08092010 | Start Date*: 2011-04-28 | ||||||||||||||||||||||||||
Sponsor Name: | ||||||||||||||||||||||||||||
Full Title: Randomised trial to investigate possible differences in biological availability and effectiveness between vitamin K solution in oil and vitamin K tablets. | ||||||||||||||||||||||||||||
Medical condition: Lowering anticoagulant effect of vitamin K antagonists in case of over-anticoagulation or pending diagnostic or therapeutic invase action. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005008-24 | Sponsor Protocol Number: 08126 | Start Date*: 2011-07-07 | ||||||||||||||||
Sponsor Name:University of Nottingham | ||||||||||||||||||
Full Title: Worms for immune regulation of multiple sclerosis | ||||||||||||||||||
Medical condition: Relapsing Multiple Sclerosis | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-002158-30 | Sponsor Protocol Number: FLUVAL AB-H-YL2011 | Start Date*: 2011-07-20 | |||||||||||
Sponsor Name:Omninvest Ltd. | |||||||||||||
Full Title: Tolerability and Immunogenicity Study of Fluval AB Influenza Vaccine (trivalent, seasonal, active ingredient content: 15 μg HA/strain/0.5 mL) in Adults and Elderly Persons | |||||||||||||
Medical condition: Immunization of healthy people against influenza virus infection. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003123-35 | Sponsor Protocol Number: TRG 10-01 | Start Date*: 2011-09-22 | |||||||||||
Sponsor Name:University of Oxford | |||||||||||||
Full Title: The impact of single versus double dose acetylsalicylic acid on platelet function in patients with type 2 diabetes (the "ASP Study"). | |||||||||||||
Medical condition: Type 2 Diabetes mellitus | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004298-24 | Sponsor Protocol Number: KCH-STR-INF | Start Date*: 2008-08-13 | |||||||||||
Sponsor Name:King's College Hospital NHS Foundation Trust [...] | |||||||||||||
Full Title: A cluster randomised trial of different strategies of antibiotic use to reduce the incidence and consequences of chest infection in acute stroke patients with swallowing problems. | |||||||||||||
Medical condition: Acute stroke patients with dysphagia and at high risk of aspiration as assessed by the bedside swallowing assessment. A policy to prevent pneumonias with prophylactic antibiotics is being investig... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001160-29 | Sponsor Protocol Number: SH-NEC-0002 | Start Date*: 2012-03-08 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: An Open Single-centre Study on the Pharmacokinetics and Pharmacodynamics of Esomeprazole After Once Daily Oral Administration for 7 Days in Preterm Infants and Neonates | |||||||||||||
Medical condition: Gastraesdophageal Reflux Disease | |||||||||||||
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Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024652-28 | Sponsor Protocol Number: OLÉ | Start Date*: 2011-08-08 | |||||||||||
Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | |||||||||||||
Full Title: Estudio para evaluar la actividad y la tolerabilidad de la biterapia con lopinavir/ritonavir y 3TC en sustitución de una triple terapia que incluya lopinavir/ritonavir y 3TC ó FTC en pacientes con ... | |||||||||||||
Medical condition: Infección VIH | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002193-23 | Sponsor Protocol Number: HLS04/2011 | Start Date*: 2011-09-27 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA L. SACCO (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
Full Title: Long term Immunogenicity of Quadrivalent Human Papillomavirus vaccine (Gardasil) in HIV-infected adolescents and young adults vs. healthy adolescents and young adults: non-randomized controlled cli... | |||||||||||||
Medical condition: HIV+ teenagers and young adults versus HIV-negative subjects: high-risk population for HPV-related disease. | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002695-16 | Sponsor Protocol Number: CA204009 | Start Date*: 2012-02-01 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase 2, Randomized Study of Bortezomib/dexamethasone With or Without Elotuzumab in Subjects with Relapsed/Refractory Multiple Myeloma. | |||||||||||||
Medical condition: Relapsed or Refractory Multiple Myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001718-32 | Sponsor Protocol Number: FBS0701CTP-07 | Start Date*: 2011-09-07 | |||||||||||
Sponsor Name:FERROKIN BIOSCIENCES INC. | |||||||||||||
Full Title: A Phase 2, Open Label, Multi-Center, Single-Dose Pharmacokinetics, and Multiple Dose Study of the Safety, Efficacy and Tolerability of FBS0701 in a Pediatric Population with Transfusional Iron Over... | |||||||||||||
Medical condition: Patients with documented transfusional iron overload ages 6 to less than 18 years old will be studied. Patients with transfusion-dependent anemias will be eligible regardless of the cause of thei... | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000637-37 | Sponsor Protocol Number: 501 | Start Date*: 2011-04-13 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA OSPEDALE S. SALVATORE | |||||||||||||
Full Title: “AN OBSERVATIONAL STUDY ON THE MOLECULES INVOLVED IN THE INTRACELLULAR UPTAKE IN PATIENTS AFFECTED FROM CHRONIC MYELOID LEUKEMIA RECEIVING TIROSINE-KINASE INHIBITORS.” | |||||||||||||
Medical condition: Chronic myeloid leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002877-46 | Sponsor Protocol Number: PALIFE-2011-01 | Start Date*: 2011-11-21 |
Sponsor Name:Fundación Renal Iñigo Álvarez de Toledo | ||
Full Title: Paricalcitol effect vs Albumine, inflammation and Fibrosis in Chronic proteinuric kidney disease patients (PALIFE trial) Randomized, controlled trial. | ||
Medical condition: Proteinuric nephropatic patients | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2011-002796-41 | Sponsor Protocol Number: NICTDP0002 | Start Date*: 2011-09-29 |
Sponsor Name:McNeil AB | ||
Full Title: A PROOF OF CONCEPT WITH A NEW NICOTINE INHALER IN COMPARISON WITH NICOTINE INHALER 10 MG - AN EXPLORATORY STUDY IN ADULT HEALTHY SMOKERS | ||
Medical condition: Tobacco Dependence | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-003425-96 | Sponsor Protocol Number: 11091 | Start Date*: 2011-12-15 |
Sponsor Name:University of Nottingham | ||
Full Title: Helicobacter eradication to prevent ulcer bleeding in aspirin users: a large simple randomised controlled trial | ||
Medical condition: Helicobacter eradication to prevent ulcer bleeding in aspirin users | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
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