- Trials with a EudraCT protocol (44,381)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
44,381 result(s) found.
Displaying page 1,278 of 2,220.
| EudraCT Number: 2005-004668-22 | Sponsor Protocol Number: SYR-322-MET-008 | Start Date*: 2006-05-26 |
| Sponsor Name:Takeda Global Research & Development Center, Inc. | ||
| Full Title: A multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Determine the Efficacy and safety of SYR110322 (SYR-322) When Used in Combination with Metformin in Subjects with Type 2 Diabetes | ||
| Medical condition: Type II diabetes mellitus. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) HU (Completed) DE (Completed) ES (Completed) CZ (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-001355-38 | Sponsor Protocol Number: AP24534-12-301 | Start Date*: 2012-10-04 |
| Sponsor Name:ARIAD Pharmaceuticals, Inc | ||
| Full Title: A Phase 3 Randomized, Open-Label Study of Ponatinib versus Imatinib in Adult Patients with Newly Diagnosed Chronic Myeloid Leukemia in Chronic Phase | ||
| Medical condition: Chronic Myeloid Leukemia in Chronic Phase | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) DE (Completed) SE (Prematurely Ended) BE (Prematurely Ended) CZ (Prematurely Ended) NL (Prematurely Ended) IT (Prematurely Ended) ES (Prematurely Ended) FI (Prematurely Ended) SK (Completed) PT (Prematurely Ended) AT (Prematurely Ended) PL (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-002022-10 | Sponsor Protocol Number: NV21928 | Start Date*: 2008-09-23 | |||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
| Full Title: Protocolo multicéntrico abierto en el que se proporciona interferón pegilado alfa-2a (PEGASYS®) en monoterapia o en combinación con ribavirina (COPEGUS®) a pacientes con hepatitis C crónica que han... | |||||||||||||
| Medical condition: Chronic hepatitis C Hepatitis C crónica | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) AT (Completed) FR (Completed) IT (Prematurely Ended) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-002781-66 | Sponsor Protocol Number: C-08-16 | Start Date*: 2008-12-04 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Alcon Research, Ltd. | ||||||||||||||||||||||||||||||||||||||
| Full Title: A twelve-month, multicenter, double-masked study of Travoprost / Brinzolamide fixed combination QD AM and Travoprost / Brinzolamide fixed combination QD PM versus COSOPT BID in patients with open-a... | ||||||||||||||||||||||||||||||||||||||
| Medical condition: Open-angle glaucoma or Ocular hypertension | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: DE (Completed) FR (Completed) ES (Completed) BE (Completed) SE (Prematurely Ended) DK (Prematurely Ended) PL (Completed) IT (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2008-001043-19 | Sponsor Protocol Number: CLO-34100405 | Start Date*: 2008-09-24 | |||||||||||
| Sponsor Name:Genzyme Europe BV | |||||||||||||
| Full Title: Phase III Randomized, Double-Blind, Controlled Study Comparing Clofarabine and Cytarabine versus Cytarabine Alone in Adult Patients 55 Years and Older with Acute Myelogenous Leukemia (AML) who have... | |||||||||||||
| Medical condition: Acute Myelogenous (Myeloid) Leukemia (AML) | |||||||||||||
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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: 2007-005886-36 | Sponsor Protocol Number: EFC6016 | Start Date*: 2008-07-03 | |||||||||||
| Sponsor Name:Sanofi -Aventis Recherche & De'veloppement | |||||||||||||
| Full Title: A randomized, double-blind, placebo-controlled, 2-arm parallel-group, multicenter study with a 24-week main treatment period and an extension assessing the efficacy and safety of AVE0010 in patient... | |||||||||||||
| Medical condition: Type II Diabetes | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) DE (Completed) FR (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-001564-31 | Sponsor Protocol Number: AMB 222 | Start Date*: 2005-10-07 | |||||||||||
| Sponsor Name:Myogen Inc. | |||||||||||||
| Full Title: A phase 2, Open-label, Multicenter Study Evaluating Ambrisentan in Subjects with Pulmonary Arterial Hypertension Who Have Previously Discontinued Endothelin Receptor Antagonist Therapy Due to Serum... | |||||||||||||
| Medical condition: Pulmonary Arterial Hypertension | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-004606-97 | Sponsor Protocol Number: PMR-EC-1209 | Start Date*: 2007-02-22 | |||||||||||
| Sponsor Name:Astellas Pharma GmbH | |||||||||||||
| Full Title: A MULTICENTER, SINGLE-ARM, OPEN, CONVERSION STUDY FROM A CYCLOSPORINE (CyA) BASED IMMUNOSUPPRESSIVE REGIMEN TO A TACROLIMUS MODFIED RELEASE, FK506E (MR4), BASED IMMUNOSUPPRESSIVE REGIMEN IN KIDNEY ... | |||||||||||||
| Medical condition: Stable, adult kidney transplant recipients (at least 12 months post transplant) who are currently treated with cyclosporine and who meet the Inclusion and Exclusion Criteria will be enrolled. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) BE (Completed) DE (Completed) ES (Completed) CZ (Completed) HU (Completed) FI (Completed) SE (Completed) DK (Completed) AT (Completed) PT (Prematurely Ended) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-000617-19 | Sponsor Protocol Number: DOXIL-BCA-3001 | Start Date*: 2004-09-13 |
| Sponsor Name:Johnson & Johnson Pharmaceutical Research and Development | ||
| Full Title: A Randomized Controlled Study of Docetaxel Monotherapy or Docetaxel and DOXIL for the Treatment of Advanced Breast Cancer | ||
| Medical condition: Breast cancer | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: HU (Completed) AT (Completed) ES (Completed) GB (Completed) DE (Completed) LT (Completed) LV (Completed) EE (Completed) IT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-003839-68 | Sponsor Protocol Number: 333369-EPY-3001/3004 | Start Date*: 2006-11-09 | |||||||||||
| Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multicenter Study to Evaluate the Efficacy, Safety and Tolerability of RWJ-333369 as Adjunctive Therapy in Subjects with Partial Onse... | |||||||||||||
| Medical condition: Partial Onset Epilepsy Seizures | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) SE (Prematurely Ended) DE (Completed) CZ (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-001490-95 | Sponsor Protocol Number: ESPRIT 002: STALWART | Start Date*: 2006-04-21 |
| Sponsor Name:National Institute of Allergy and Infectious Diseases (NIAID) | ||
| Full Title: A Randomized, Open-Label, International Study of Subcutaneous Recombinant Interleukin-2 (rIL-2, Aldesleukin) with and without Concomitant Antiretroviral Therapy in Patients with HIV-1 Infection and... | ||
| Medical condition: HIV infection | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) ES (Completed) PT (Completed) DE (Completed) IT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-000025-19 | Sponsor Protocol Number: A0081183 | Start Date*: 2008-05-12 | |||||||||||
| Sponsor Name:Pfizer, S.A. | |||||||||||||
| Full Title: "ESTUDIO DE PREGABALINA, ALEATORIZADO, DOBLE CIEGO, DE 6 SEMANAS DE DURACIÓN EN SUJETOS CON SÍNDROME DE PIERNAS INQUIETAS" RANDOMIZED, DOUBLE-BLIND, 6-WEEK STUDY OF PREGABALIN IN SUBJECTS WITH RES... | |||||||||||||
| Medical condition: "Síndrome de Piernas Inquietas (SPI)" Restless legs syndrome (RLS) | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) AT (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-014916-37 | Sponsor Protocol Number: A3051122 | Start Date*: 2010-03-15 | |||||||||||
| Sponsor Name:PFIZER | |||||||||||||
| Full Title: "Estudio de fase 4, doble ciego, controlado con placebo, multicéntrico y de 12 semanas de duración para evaluar la seguridad y la eficacia del tartrato de Vareniclina (CP-526,555) 1 mg dos veces a... | |||||||||||||
| Medical condition: "Dejar de Fumar" "Smoking cessation" | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) DE (Completed) HU (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-006497-15 | Sponsor Protocol Number: LD | Start Date*: 2009-10-14 |
| Sponsor Name:Wilhelminen Krebsforschung GmbH | ||
| Full Title: Lenalidomide and Dexamethasone for treatment of patients with acute myeloma (light chain)-induced renal failure | ||
| Medical condition: There are two patient groups to be included into the study: 1) Patients with previously unknown MM and acute light chain induced renal failure 2) Patients with previously diagnosed MM, normal or... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) CZ (Completed) SK (Completed) DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-017238-39 | Sponsor Protocol Number: IPX066-B09-06 | Start Date*: 2010-09-15 | |||||||||||
| Sponsor Name:Impax Laboratories, Inc., acting through its Impax Pharmaceuticals Division (Impax) | |||||||||||||
| Full Title: A Study to Compare IPX066 and Carbidopa/Levodopa/Entacapone (CLE) in Advanced Parkinson’s Disease | |||||||||||||
| Medical condition: Idiopathic Parkinson’s Disease (paralysis agitans) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) IT (Completed) BE (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-019844-38 | Sponsor Protocol Number: A6141116 | Start Date*: 2010-08-12 | |||||||||||
| Sponsor Name:Pfizer, S.A | |||||||||||||
| Full Title: A double-blind, randomized, placebo-controlled trial evaluating the safety and efficacy of early the treatment with Eplerenone in patients with acute myocardial infarction. Estudio doble ciego, al... | |||||||||||||
| Medical condition: Infarto agudo de miocardio | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) SK (Completed) CZ (Completed) HU (Completed) GB (Completed) DE (Completed) NL (Completed) GR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-005232-33 | Sponsor Protocol Number: FE200486 CS30 | Start Date*: 2009-04-15 | |||||||||||
| Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
| Full Title: A randomised, parallel arm, open-label trial comparing degarelix with goserelin plus anti-androgen flare protection (bicalutamide), in terms of prostate size reduction in prostate cancer patients o... | |||||||||||||
| Medical condition: Prostate Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: NL (Completed) DE (Completed) FR (Completed) ES (Completed) GB (Completed) GR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-001841-40 | Sponsor Protocol Number: GW685698X | Start Date*: 2005-10-05 |
| Sponsor Name:GlaxoSmithKline Research And Development Ltd | ||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multicenter Study to Evaluate the Efficacy and Safety of GW685698X Inhalation Powder 200mcg Twice-Daily, GW685698X Inhalation Powder ... | ||
| Medical condition: Persistent asthma | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: CZ (Completed) LV (Prematurely Ended) DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-015400-26 | Sponsor Protocol Number: ARQ 197-A-U251 | Start Date*: 2010-03-04 | |||||||||||
| Sponsor Name:Daiichi Sankyo Pharma Development | |||||||||||||
| Full Title: MULTICENTER PHASE 2 TRIAL OF ARQ 197 FOR SUBJECTS WITH RELAPSED OR REFRACTORY GERM CELL TUMORS | |||||||||||||
| Medical condition: Germ cell tumors (GCT) including testicular and non-central nervous system (non-CNS) extragonadal types. | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: DE (Completed) FR (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-014246-29 | Sponsor Protocol Number: BPS-MR-PAH-203 | Start Date*: 2010-02-01 | |||||||||||
| Sponsor Name:Lung Rx | |||||||||||||
| Full Title: A 12-week, double-blind, international, multicenter, dose-response study of the safety and efficacy of Beraprost Sodium Modified Release (BPS-MR) in patients with pulmonary arterial hypertension (PAH) | |||||||||||||
| Medical condition: Pulmonary Arterial Hypertension | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (Completed) BE (Prematurely Ended) DE (Completed) CZ (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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