- Trials with a EudraCT protocol (2,279)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
2,279 result(s) found for: slovakia.
Displaying page 1 of 114.
EudraCT Number: 2008-003980-38 | Sponsor Protocol Number: ML 21800 | Start Date*: 2008-09-22 |
Sponsor Name:Roche Slovensko s.r.o. | ||
Full Title: An open label study of the effect of Xeloda and radiotherapy on pathological response rate in patients with locally advanced rectal cancer. | ||
Medical condition: Locally advanced rectal cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-011520-53 | Sponsor Protocol Number: ML 22508 | Start Date*: 2009-05-04 |
Sponsor Name:Roche Slovensko s.r.o. | ||
Full Title: Evaluation of Adherence and Persistence to Tocilizumab in combination with Methotrexate or Tocilizumab Monotherapy in patients with moderate to severe active rheumatoid arthritis in local environment | ||
Medical condition: moderate to severe active rheumatoid arthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-005946-35 | Sponsor Protocol Number: EFC10096 | Start Date*: 2007-05-17 |
Sponsor Name:sanofi-aventis recherche & développement | ||
Full Title: Efficacy and safety of 3 intra-articular injections of 500 µg icatibant in a randomized, double-blind, parallel-group, placebo-controlled 13-week multi-centre study in patients with symptomatic kne... | ||
Medical condition: patients with painful OA in the knee | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-002456-18 | Sponsor Protocol Number: 758-CL-010 | Start Date*: 2006-04-21 | |||||||||||
Sponsor Name:Astellas Pharma Europe B.V. | |||||||||||||
Full Title: A RANDOMIZED, DOUBLE BLIND, PLACEBO CONTROLLED STUDY TO EVALUATE THE SAFETY, TOLERABILITY AND PRELIMINARY EFFICACY OF A FOUR-WEEK TREATMENT WITH YM758 IN SUBJECTS WITH STABLE ANGINA. | |||||||||||||
Medical condition: Stable angina pectoris | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004854-19 | Sponsor Protocol Number: DSC/03/2357/06 | Start Date*: 2005-04-25 |
Sponsor Name:Italfarmaco S.p.A. | ||
Full Title: A randomized, double-blind, placebo-controlled, parallel group multicenter study to investigate efficacy and safety of ITF 2357 in the management of patients with active moderate to severe Crohn’s ... | ||
Medical condition: Crohn's disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001216-29 | Sponsor Protocol Number: PRCL-PoC | Start Date*: 2018-09-11 | |||||||||||
Sponsor Name:PRCL Research Inc. | |||||||||||||
Full Title: A Phase 2a Study to Evaluate Safety, Tolerability, and Efficacy of PRCL-02 in Patients with Moderate to Severe Chronic Plaque Psoriasis | |||||||||||||
Medical condition: Patients with moderate to severe chronic plaque psoriasis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004370-85 | Sponsor Protocol Number: 104083 | Start Date*: 2005-01-25 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A phase III, multicentric open study to evaluate the immunological memory induced by a 3-dose primary vaccination followed by a booster dose with GSK Biologicals’ 11-valent conjugate pneumococcal v... | ||
Medical condition: A single dose of Aventis Pasteur’s 23-valent pneumococcal polysaccharide vaccine (Pneumo 23) to healthy children who were either primed with the 3-dose primary vaccination followed by the booster d... | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-004981-42 | Sponsor Protocol Number: GCTSK001 | Start Date*: 2008-01-17 |
Sponsor Name:Narodny onkologicky ustav | ||
Full Title: Phase II study of sunitinib malate (SUTENT®) in relapsed germ cell tumors in males. | ||
Medical condition: germ cell tumor | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-003001-94 | Sponsor Protocol Number: MSGLP | Start Date*: 2019-11-06 | |||||||||||
Sponsor Name:Lekárska fakulta UK Bratislava | |||||||||||||
Full Title: Use of GLP-1 analogs in the treatment of multiple sclerosis | |||||||||||||
Medical condition: Our hypothesis is that patients with MS have a disorder of energy metabolism in neurons and glial cells of the CNS, contributing to the development and progression of demyelinating foci and neurode... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001270-33 | Sponsor Protocol Number: GCTSK003 | Start Date*: 2015-07-28 | |||||||||||
Sponsor Name:Národný onkologický ústav | |||||||||||||
Full Title: A treatment strategy of the Use of 1st line Chemotherapy in Patients with Poor-Prognosis Disseminated Non-Seminomatous Germ Cell Tumors based on tumor marker decline: A Phase II Trial of paclitaxel... | |||||||||||||
Medical condition: Disseminated Non-Seminomatous Germ Cell Tumors. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003384-30 | Sponsor Protocol Number: IR902-231 | Start Date*: 2007-02-26 |
Sponsor Name:The Immune Response Corporation | ||
Full Title: A Phase II Study of NeuroVax™, a Therapeutic TCR Peptide Vaccine for Multiple Sclerosis | ||
Medical condition: Multiple Sclerosis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-001860-36 | Sponsor Protocol Number: V00114CP3042A | Start Date*: 2008-05-29 |
Sponsor Name:Pierre Fabre Médicament | ||
Full Title: EFFICACY AND SAFETY STUDY OF THE ANTIHISTAMINE V0114CP 2.5MG IN THE TREATMENT OF SEASONAL ALLERGIC RHINITIS. RANDOMISED, DOUBLE-BLIND, THREE ARM PARALLEL GROUP STUDY INCLUDING PLACEBO AND ACTIVE CO... | ||
Medical condition: The medical condition to be investigated in this study is the seasonall allergic rhinitis. The intendent indication for the product is the treatment of allergic rhinitis. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-004412-12 | Sponsor Protocol Number: CLAF237B2201 | Start Date*: 2009-02-27 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A multi-center, randomized, double-blind study to evaluate the efficacy and long-term safety of vildagliptin modified release (MR) as monotherapy in patients with type 2 diabetes | ||
Medical condition: Type II Diabetes | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-001224-19 | Sponsor Protocol Number: 1/0196/16 | Start Date*: 2019-02-11 | ||||||||||||||||||||||||||
Sponsor Name:Lekárska fakulta Univerzity Komenského v Bratislave | ||||||||||||||||||||||||||||
Full Title: Non-invasive in-vivo prediction of therapeutic response to inhibitors of angiogenesis using gallium (68Ga) NODAGA-RGD PET/CT | ||||||||||||||||||||||||||||
Medical condition: Advanced metastatic cancer of the colon or rectum | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: SK (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016911-39 | Sponsor Protocol Number: 113954 | Start Date*: 2010-05-05 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: An open, phase IV, multicentre, study to assess the long-term persistence of antibodies against hepatitis B and the immune response to a hepatitis B vaccine challenge in healthy children aged 11-12... | ||
Medical condition: Antibody persistence and hepatitis B vaccine challenge at 11-12 years of age (excluding 13th birthday), after primary vaccination with GSK Biologicals’ DTPa-HBV-IPV/Hib vaccine (Infanrix hexa) or G... | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-005199-90 | Sponsor Protocol Number: RHB-104-04 | Start Date*: 2019-02-14 | |||||||||||
Sponsor Name:RedHill Biopharma Ltd. | |||||||||||||
Full Title: An Open Label Study to Assess the Efficacy and Safety of Fixed-Dose Combination RHB-104 in Subjects with Active Crohn’s Disease Despite 26 Weeks of Participation in the MAP US RHB-104-01 Study | |||||||||||||
Medical condition: Moderately to Severely Active Crohn's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001502-10 | Sponsor Protocol Number: GCTSK002 | Start Date*: 2011-09-28 |
Sponsor Name:National Cancer Institute | ||
Full Title: Phase II study of Everolimus in refractory testicular germ cell cancer. | ||
Medical condition: refractory metastatic germ cell tumors | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-004372-19 | Sponsor Protocol Number: HARRAS1/2012 | Start Date*: 2013-06-05 |
Sponsor Name:HARRAS-PHARMA-CURARINA GmbH | ||
Full Title: Comparative Study with a Propolis Cream vs. Aciclovir Cream in Patients with Herpes labialis A double-blind, randomised, two-arm study | ||
Medical condition: Herpes labialis Double-blind, randomised, controlled parallel group comparison of a Propolis special extract GH 2002 cream (Herpetino® Balsam) and an aciclovir 5% containing cream. Up to 10 day... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-005015-40 | Sponsor Protocol Number: IVER-303 | Start Date*: 2021-04-29 | |||||||||||
Sponsor Name:Chemo Research S.L. | |||||||||||||
Full Title: A multicentre, phase III, double-blind, randomised, parallel, placebo-controlled trial to assess efficacy and safety of early administration of Ivermectin during 3 consecutive days to prevent SARS ... | |||||||||||||
Medical condition: Coronavirus disease (COVID-19) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003554-15 | Sponsor Protocol Number: 18031977 | Start Date*: 2006-11-09 |
Sponsor Name:National Cancer Institute | ||
Full Title: The histone deacetylase inhibitor (HDAC) valproic acid as second line treatment for hormone refractory metastatic prostate cancer. A phase II. study. | ||
Medical condition: hormone refractory metastatic prostate cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: SK (Completed) | ||
Trial results: View results |
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