- Trials with a EudraCT protocol (39,306)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
39,306 result(s) found for: $1.
Displaying page 1,596 of 1,966.
| EudraCT Number: 2005-003432-22 | Sponsor Protocol Number: EGF104383 | Start Date*: 2008-07-03 | |||||||||||
| Sponsor Name:Glaxo SmithKline Research and Development Limited | |||||||||||||
| Full Title: A Randomized, Double Blind, Placebo-Controlled, Multicenter, Phase III Study Comparing the Activity of Paclitaxel Plus Trastuzumab Plus Lapatinib to Paclitaxel Plus Trastuzumab Plus Placebo in Wome... | |||||||||||||
| Medical condition: ErbB2+ Metastatic Breast Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-003250-29 | Sponsor Protocol Number: IPAB-07-002 | Start Date*: 2008-03-14 | |||||||||||
| Sponsor Name:Independent Pharmaceutica AB | |||||||||||||
| Full Title: A randomised, placebo-controlled, multi-centre study on the efficacy of Niccine, a vaccine for nicotine, in smoking relapse prevention, assessed in abstinent, adult smokers. | |||||||||||||
| Medical condition: The intended indication for the drug under investigation is smoking relapse prevention. Tobacco smoking has been identified as the single largest preventable cause of morbidity and premature death ... | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-001530-14 | Sponsor Protocol Number: NPC 2006 | Start Date*: 2007-10-12 | |||||||||||
| Sponsor Name:GORTEC [...] | |||||||||||||
| Full Title: Essai de Phase III, Multicentrique, Randomisé, comparant la Chimiothérapie d’induction par Docétaxel, Cisplatine et 5-Fluorouracile (TPF) suivie d’une chimio-radiothérapie concomitante versus une c... | |||||||||||||
| Medical condition: Patients atteints de cancers du nasopharynx classés T2b; T3;T4 ; OMS II-III et /ou avec envahissement ganglionnaire (Nsupérieur ou égal à 1) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-005931-27 | Sponsor Protocol Number: D1690C00005 | Start Date*: 2008-04-17 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A 24-Week Randomised, Double-blind, Parallel-group, Multi-centre, Placebo-controlled Phase III Study to Evaluate the Efficacy and Safety of Dapagliflozin in Combination with Glimepiride (a Sulphony... | |||||||||||||
| Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) PL (Completed) CZ (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-007587-21 | Sponsor Protocol Number: CLL10 | Start Date*: 2008-09-05 | |||||||||||
| Sponsor Name:University of Cologne | |||||||||||||
| Full Title: Phase III trial of combined immunochemotherapy with Fludarabine, Cyclophosphamide and Rituximab (FCR) versus Bendamustine and Rituximab (BR) in patients with previously untreated chronic lymphocyti... | |||||||||||||
| Medical condition: patients (age 18 years or older) with chronic lymphocytic leukemia: Stage Binet C or stage Binet B and A requiring treatment | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) AT (Completed) DK (Completed) CZ (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-000123-26 | Sponsor Protocol Number: PRODIGE 10/VA 2007-40 | Start Date*: 2008-07-31 | |||||||||||
| Sponsor Name:Centre Val d'Aurelle Paul Lamarque | |||||||||||||
| Full Title: Etude de phase II, randomisée, testant l'association Nexavar (sorafenib) gemcitabine et oxaliplatine (GEMOX) dans le traitement des carcinomes hépatocellulaires non accessibles à un traitement chir... | |||||||||||||
| Medical condition: Carcinome hépatocellulaire non accessible à une chirurgie ou à une destruction per-cutanée. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-003285-26 | Sponsor Protocol Number: ASTA | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Universität Mainz, Klinik und Poliklinik für Kinder- und Jugendpsychiatrie und -psychotherapie | |||||||||||||
| Full Title: Effect of methylphenidate formulation on ADHD-patients' adherence to medical treatment. A comparison of Medikinet retard® (ER) once daily and Medikinet® (IR) twice daily in children and adolescents... | |||||||||||||
| Medical condition: Effect of methylphenidate formulation on ADHD-patients adherence to treatment | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-005613-19 | Sponsor Protocol Number: R-COMP 14 | Start Date*: 2007-04-27 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA OSPEDALE S. SALVATORE | |||||||||||||
| Full Title: R-COMP 14 in elderly patients with high grade non-Hodgkin lymphoma | |||||||||||||
| Medical condition: Elderly patients with B non-Hodgkin lymphoma | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-004220-23 | Sponsor Protocol Number: VIDEAT | Start Date*: 2008-09-04 | |||||||||||
| Sponsor Name:AZIENDA SANITARIA OSPEDALIERA "S. GIOVANNI BATTISTA DI TORINO" | |||||||||||||
| Full Title: EFFECT OF SUPPLEMENTATION WITH CHOLECALCIFEROL ON GLUCOSE AND LIPID METABOLISM, BLOOD PRESSURE, BONE MASS, QUALITY OF LIFE, CARDIOVASCULAR MORBIDITY AND MORTALITY IN PATIENTS WITH ISCHAEMIC HEART D... | |||||||||||||
| Medical condition: ISCHAEMIC ARTERY DISEASE | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-002828-15 | Sponsor Protocol Number: S 379 | Start Date*: 2009-03-13 |
| Sponsor Name:Krankenhaus Nordwest GmbH | ||
| Full Title: An open-label, uncontrolled phase II trial of single agent sunitinib (SU 11248) for patients with chemo-refractory metastatic melanoma | ||
| Medical condition: chemo-refractory metastatic melanoma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-006175-75 | Sponsor Protocol Number: BRD 08/9-P | Start Date*: 2008-12-24 | |||||||||||
| Sponsor Name:CHU de Nantes | |||||||||||||
| Full Title: ETUDE DE PHASE II D’UN CONDITIONNEMENT SUB-MYELOABLATIF A TOXICITE REDUITE AVANT ALLOGREFFE DE CELLULES SOUCHES HEMATOPOÏETIQUES DANS LE TRAITEMENT DES HEMOPATHIES MALIGNES | |||||||||||||
| Medical condition: Hémopathies malignes | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-001712-21 | Sponsor Protocol Number: ESBA105CRD02 | Start Date*: 2009-03-05 | |||||||||||
| Sponsor Name:Delenex Therapeutics AG | |||||||||||||
| Full Title: A double-blind, randomised placebo-controlled Phase I/IIa study to investigate the safety, tolerability and efficacy on pain of intra-articular ESBA105 applied to patients with severely painful os... | |||||||||||||
| Medical condition: Osteoarthritis of the knee | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-002775-28 | Sponsor Protocol Number: GBM - ANOCEF01 | Start Date*: 2008-10-06 | |||||||||||
| Sponsor Name:Centre Georges François Leclerc | |||||||||||||
| Full Title: Evaluation de l'association irinotécan/bévacizumab utilisée en néo-adjuvant et en adjuvant d'une radiochimiothérapie avec témozolomide concomitant pour les glioblastomes non résécables. Etude de ph... | |||||||||||||
| Medical condition: GLIOBLASTOMES MULTIFORME (GBM) NON RESECABLES | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-008339-27 | Sponsor Protocol Number: A0081107 | Start Date*: 2009-05-07 | |||||||||||
| Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, NY10017 | |||||||||||||
| Full Title: A 17-WEEK, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP, MULTI-CENTER TRIAL OF PREGABALIN FOR THE TREATMENT OF CHRONIC CENTRAL NEUROPATHIC PAIN AFTER SPINAL CORD INJURY | |||||||||||||
| Medical condition: Chronic Central Neuropathic Pain after Spinal Cord Injury. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-001916-18 | Sponsor Protocol Number: 20080331 | Start Date*: 2008-11-05 | ||||||||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA ORDINE MAURIZIANO | ||||||||||||||||||
| Full Title: A phase II, randomized trial with single agent trastuzumab or lapatinib in women with metastatic breast cancer iperexpressing HER2 | ||||||||||||||||||
| Medical condition: women with metastatic breast cancer iperexpressing HER2 | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: IT (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2007-006603-20 | Sponsor Protocol Number: C1377T04 | Start Date*: 2009-07-29 | |||||||||||
| Sponsor Name:Centocor B.V. | |||||||||||||
| Full Title: A Phase 2, 2-Part, Multicenter, Randomized, Double-blind, Parallel-group, Placebo-controlled, Proof-of-concept, dose-finding Study Evaluating the Efficacy and Safety of CNTO 136 Administered Subcut... | |||||||||||||
| Medical condition: Rheumatoid Arthritis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-003866-16 | Sponsor Protocol Number: AP REN 01-01 | Start Date*: 2009-03-03 | ||||||||||||||||
| Sponsor Name:AM-Pharma B.V. | ||||||||||||||||||
| Full Title: A Phase-II, double-blind, randomized, placebo-controlled proof of concept study on the safety and early efficacy of Alkaline Phosphatase in sepsis patients with Renal Failure. | ||||||||||||||||||
| Medical condition: Sepsis with Renal Failure | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2009-010399-10 | Sponsor Protocol Number: STAT | Start Date*: 2009-04-16 | ||||||||||||||||
| Sponsor Name:OSPEDALE G.PASQUINUCCI-FONDAZIONE G.MONASTERIO | ||||||||||||||||||
| Full Title: STANDARD VERSUS TAILORED ANTI-PLATELET THERAPY IN ACS PATIENTS UNDERGOING PERCUTANEOUS CORONARY ANGIOPLASTY | ||||||||||||||||||
| Medical condition: PATIENTS UNDERGOING CORONARY ANGIOPLASTY FOR ACUTE CORONARY SYNDROME TYPE STEMI / NSTEMI ESC | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2009-010327-41 | Sponsor Protocol Number: EBEV | Start Date*: 2010-02-23 | ||||||||||||||||
| Sponsor Name:Fundació Privada Clínic per a la Recerca Biomèdica | ||||||||||||||||||
| Full Title: Estudio aleatorizado y abierto de la eficacia, seguridad y tolerabilidad de dosis repetidas de bevacizumab intravítreo en pacientes con edema macular uveítico | ||||||||||||||||||
| Medical condition: Edema macular uveítico | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2009-016849-25 | Sponsor Protocol Number: A0081047 | Start Date*: 2010-03-15 | |||||||||||
| Sponsor Name:Pfizer Inc | |||||||||||||
| Full Title: A DOUBLE-BLIND, RANDOMIZED, MULTICENTER EFFICACY AND SAFETY STUDY OF PREGABALIN (LYRICA) AS MONOTHERAPY IN PATIENTS WITH PARTIAL SEIZURES | |||||||||||||
| Medical condition: Partial Seizures | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
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