- Trials with a EudraCT protocol (44,334)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
44,334 result(s) found.
Displaying page 910 of 2,217.
EudraCT Number: 2012-001106-26 | Sponsor Protocol Number: EC11-444-OSTEOSARC | Start Date*: 2012-07-02 |
Sponsor Name:JAVIER MARTÍN BROTO | ||
Full Title: PHASE II MULTICENTRIC AND PROSPECTIVE TRIAL WITH GEMCITABINE AND RAPAMYCIN IN SECOND LINE OF METASTATIC OSTEOSARCOMA | ||
Medical condition: Patients diagnosed with metastatic osteosarcoma cancer types that have been treated with chemotherapy and have active disease that permits to receive this treatment combination. | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-001638-41 | Sponsor Protocol Number: CLAR-09007 | Start Date*: 2011-10-12 |
Sponsor Name:CLARUS THERAPEUTICS, INC. | ||
Full Title: PHASE III, ACTIVE-CONTROLLED, SAFETY AND EFFICACY TRIAL OF ORAL TESTOSTERONE UNDECANOATE (TU) IN HYPOGONADAL MEN. | ||
Medical condition: Hypogonadal men | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: DE (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-005398-22 | Sponsor Protocol Number: ARACONDRO-001 | Start Date*: 2012-10-11 | |||||||||||
Sponsor Name:ARAFARMA GROUP, S.A. | |||||||||||||
Full Title: A randomized, multicenter, double-blind, double dummy and parallel study to evaluate the efficacy of the combination of Chondroitin sulfate and Glucosamine hydrochloride in a single dose chewable t... | |||||||||||||
Medical condition: Knee osteoarthritis with moderate to severe pain. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005007-33 | Sponsor Protocol Number: BIBEC02 | Start Date*: 2012-02-17 | |||||||||||
Sponsor Name:Laboratorios Biomendi S.A.U. | |||||||||||||
Full Title: A multicenter, randomized, double-blind, parallel groups, placebo-controlled trial to evaluate efficacy and safety of a new i.v. formulation of ibuprofen 800 mg every 6 hours in the management of p... | |||||||||||||
Medical condition: Moderate to severe postoperative pain. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000311-87 | Sponsor Protocol Number: FFC-0001 | Start Date*: 2012-04-23 | |||||||||||
Sponsor Name:Fundación Fernández-Cruz | |||||||||||||
Full Title: A long-term, randomized, open-labeled, parallel-group trial to compare the effects of liraglutide and sulphonilurea both in combination with metformin on clinical, endothelial and image markers of ... | |||||||||||||
Medical condition: type 2 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001296-36 | Sponsor Protocol Number: PCTA206/11 | Start Date*: 2012-03-09 |
Sponsor Name:Photocure ASA | ||
Full Title: A double blinded, prospective, randomized, vehicle controlled, multi-center study of photodynamic therapy with Visonac cream in patients with acne vulgaris | ||
Medical condition: acne vulgaris | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2011-004449-42 | Sponsor Protocol Number: A3L24 | Start Date*: 2012-04-10 | ||||||||||||||||||||||||||
Sponsor Name:Sanofi Pasteur S.A | ||||||||||||||||||||||||||||
Full Title: Multi-center, randomized, observer blinded, Phase III trial in 1,376 infants, using Infanrix hexa™ as the control vaccine. Four-arm trial with subjects randomly allocated to receive 1 of 3 lots of ... | ||||||||||||||||||||||||||||
Medical condition: Prevention of infections caused by Corynebacterium diphtheriae, Clostridium tetani, Bordetella pertussis, poliovirus types 1, 2 and 3, prevention against invasive infections caused by Haemophilus i... | ||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: Outside EU/EEA | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-001980-53 | Sponsor Protocol Number: GORTX-2012 | Start Date*: 2012-05-15 | |||||||||||
Sponsor Name:FONDAZIONE IRCCS CA' GRANDA OSPEDALE MAGGIORE POLICLINICO DI MILANO | |||||||||||||
Full Title: Preliminary study on the effectiveness of low doses of Rituximab in patients with Graves’ orbitopathy (GO) poorly responding to immunosuppressive steroid treatment. | |||||||||||||
Medical condition: Active moderate to severe Graves Orbitopathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001365-40 | Sponsor Protocol Number: BP25619 | Start Date*: 2012-02-08 | |||||||||||
Sponsor Name:F.Hoffmann-La Roche | |||||||||||||
Full Title: A Multi-Center, Randomized, Double-Blind, Placebo-Controlled Study Evaluating the Efficacy and Safety of 2 Doses of RO4905417 (R1512) Administered to Patients with Non ST-Elevation Myocardial Infar... | |||||||||||||
Medical condition: Non-STEMI | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005887-20 | Sponsor Protocol Number: MRZ60201_3076_1 | Start Date*: 2012-07-17 | |||||||||||
Sponsor Name:Merz Pharmaceuticals GmbH | |||||||||||||
Full Title: A prospective, randomized, double-blind, placebo-controlled, multicenter study with an open-label extension period to investigate the efficacy and safety of NT 201 in the combined treatment of uppe... | |||||||||||||
Medical condition: Upper facial lines (horizontal forehead lines, glabellar frown lines, and lateral periorbital lines) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000868-15 | Sponsor Protocol Number: PENT_PTA | Start Date*: 2012-03-06 | |||||||||||
Sponsor Name:UNIVERSITA' CAMPUS BIOMEDICO | |||||||||||||
Full Title: EFFECT OF TREATMENT WITH PENTOXIFYLLINE ABOUT THE RISK RATER OF POST-angioplasty restenosis IN PATIENTS WITH LOWER LIMB arterial disease | |||||||||||||
Medical condition: PERIPHERAL ARTERIOPATHY | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002281-12 | Sponsor Protocol Number: CT-BI-Vacc-4x-2012/1 | Start Date*: 2013-02-01 | |||||||||||
Sponsor Name:Bionor Immuno AS | |||||||||||||
Full Title: Re-boosting of Subjects Previously Included in the CT BI-Vacc-4x 2007/1 Study. An Open, Multicenter, Immunogenicity, Follow-up Reboosting Study with Vacc-4x in Subjects Infected with HIV-1 Who Have... | |||||||||||||
Medical condition: Subjects Infected with HIV-1 Who Have Maintained an Adequate Response to ART | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) ES (Ongoing) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004763-72 | Sponsor Protocol Number: IM133-005 | Start Date*: 2012-06-26 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase IIb, Double-Blind, Randomized, Placebo-Controlled, Double-Dummy, Dose-Ranging Study to Evaluate the Clinical Efficacy and Safety of Induction and Maintenance Therapy with BMS-945429 in Subj... | |||||||||||||
Medical condition: Crohn’s Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) AT (Completed) DE (Completed) CZ (Prematurely Ended) NL (Prematurely Ended) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002128-41 | Sponsor Protocol Number: RyB001 | Start Date*: 2011-07-12 |
Sponsor Name:Erasmus MC | ||
Full Title: Accumulation of Nadroparin Used in Renal Insufficiency Assessed by anti-Xa levels | ||
Medical condition: Venous thromboembolism | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005219-98 | Sponsor Protocol Number: PH3-01 | Start Date*: 2012-10-08 | |||||||||||
Sponsor Name:Galena Biopharma, Inc | |||||||||||||
Full Title: Prevention of Recurrence in Early-Stage, Node-Positive Breast Cancer with Low to Intermediate HER2 Expression with NeuVax™ Treatment (PRESENT) | |||||||||||||
Medical condition: Operable early-stage, node-positive breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BG (Prematurely Ended) HU (Prematurely Ended) CZ (Prematurely Ended) DE (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000831-10 | Sponsor Protocol Number: E5501-G000-305 | Start Date*: 2012-07-16 | ||||||||||||||||||||||||||
Sponsor Name:Eisai Limited | ||||||||||||||||||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-blind, Active-controlled, Parallel-group Trial with an Open-label Extension Phase to Evaluate the Efficacy and Safety of Oral E5501 versus Eltrombopag, i... | ||||||||||||||||||||||||||||
Medical condition: Chronic Immune Thrombocytopenia (Idiopathic Thrombocytopenic Purpura) | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: BE (Prematurely Ended) DE (Prematurely Ended) AT (Prematurely Ended) NL (Prematurely Ended) GB (Prematurely Ended) ES (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-001465-33 | Sponsor Protocol Number: PGL11-024 | Start Date*: 2012-07-09 | |||||||||||
Sponsor Name:PregLem S.A. | |||||||||||||
Full Title: A Phase III, multicentre, extension study investigating the efficacy and safety of repeated intermittent 3-month courses of open-label administration of ulipristal acetate, in subjects with symp... | |||||||||||||
Medical condition: Uterine myomas are benign, monoclonal, hormone-sensitive, smooth muscle tumours of the uterus. They are the most common tumour of the female reproductive tract in pre-menopausal women and mostly a... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) AT (Completed) ES (Ongoing) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005577-23 | Sponsor Protocol Number: 853-P-401 | Start Date*: 2012-07-09 | |||||||||||
Sponsor Name:Novartis Consumer Health | |||||||||||||
Full Title: A randomized, double-blind, multi-center, placebo-controlled, parallel group study to evaluate the efficacy and safety of diclofenac potassium 25 mg in subjects with acute joint pain | |||||||||||||
Medical condition: ankle sprain, grade I - II | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001597-33 | Sponsor Protocol Number: 20081203 | Start Date*: 2009-06-18 | |||||||||||
Sponsor Name:University Medical Center Utrecht | |||||||||||||
Full Title: Development of chronic disease in newly diagnosed Idiopathic Thrombocytopenic Purpura of Childhood. A randomized controlled study on the influence of treatment with intravenous gammaglobulin on the... | |||||||||||||
Medical condition: Acute Idiopathic Thrombocytopenic Purpura (ITP) in children | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004840-30 | Sponsor Protocol Number: TREAT | Start Date*: 2006-07-26 | |||||||||||
Sponsor Name:Thoraxklinik Heidelberg | |||||||||||||
Full Title: ADJUVANT CHEMOTHERAPY WITH PEMETREXED AND CISPLATIN vs. VINORELBINE AND CISPLATIN IN NSCLC IB, IIA, IIB, T3N1: A RANDOMIZED PHASE II STUDY | |||||||||||||
Medical condition: Patients with pathologically confirmed, R0 resected non-small cell lung cancer (NSCLC), pathologic stage IB, IIA, IIB, T3N1 (without need for further radiotherapy); systematic lymph node dissection... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) | |||||||||||||
Trial results: (No results available) |
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