- Trials with a EudraCT protocol (354)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
354 result(s) found for: Bridge therapy.
Displaying page 1 of 18.
EudraCT Number: 2017-001366-14 | Sponsor Protocol Number: 207757 | Start Date*: 2017-09-14 | |||||||||||
Sponsor Name:GLAXOSMITHKLINE RESEARCH AND DEVELOPMENT | |||||||||||||
Full Title: A long-term safety and efficacy follow-on study in participants with transfusion dependent β-thalassemia who have previously received GSK2696277 (autologous hematopoietic stem cells genetically mod... | |||||||||||||
Medical condition: Beta-thalassemia | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001644-29 | Sponsor Protocol Number: SAS115359 | Start Date*: 2012-05-04 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: SAS115359, a Safety and Efficacy Study of Inhaled Fluticasone Propionate/Salmeterol Combination versus Inhaled Fluticasone Propionate in the Treatment of Adolescent and Adult Subjects with Asthma. | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) AT (Completed) DE (Completed) ES (Completed) LT (Completed) SE (Completed) LV (Completed) HU (Completed) CZ (Completed) BE (Completed) NL (Completed) PL (Completed) IT (Completed) DK (Completed) SK (Completed) FI (Prematurely Ended) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001643-79 | Sponsor Protocol Number: SAS115358 | Start Date*: 2012-01-24 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: A 6-month safety and benefit study of inhaled fluticasone propionate/ salmeterol combination versus inhaled fluticasone propionate in the treatment of 6,200 pediatric subjects 4-11 years old with p... | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) GB (Completed) LV (Completed) CZ (Completed) LT (Completed) ES (Completed) AT (Completed) SE (Not Authorised) BE (Completed) DK (Completed) NL (Completed) BG (Completed) IT (Completed) FI (Prematurely Ended) SK (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002484-99 | Sponsor Protocol Number: 2006 | Start Date*: 2007-01-10 |
Sponsor Name:South Devon Health Care NHS Foundation Trust | ||
Full Title: The Use of Nebulised Magnesium Sulphate in Exacerbations of Chronic Obstructive Pulmonary Disease (COPD) | ||
Medical condition: We propose a study to examine whether adjuvant magnesium therapy administered via nebuliser is effective in the management of patients with acute exacerbations of COPD. The findings should help to ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-001643-51 | Sponsor Protocol Number: MEA115666 | Start Date*: 2012-09-17 |
Sponsor Name:GlaxoSmithKline Research and Development Limited | ||
Full Title: MEA115666: A multi-centre, open-label, long term safety study of mepolizumab in asthmatic subjects who participated in the MEA112997 trial. | ||
Medical condition: Subjects with severe, refractory asthma and a history of eosinophilic inflammation. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-000657-50 | Sponsor Protocol Number: PM1116197 | Start Date*: 2014-05-27 | ||||||||||||||||||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | ||||||||||||||||||||||||||||
Full Title: A Clinical Outcomes Study to Compare the Incidence of Major Adverse Cardiovascular Events in Subjects Presenting with Acute Coronary Syndrome Treated with Losmapimod Compared to Placebo (PM1116197)... | ||||||||||||||||||||||||||||
Medical condition: | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: SE (Completed) NL (Prematurely Ended) IT (Completed) DE (Completed) BE (Completed) SK (Completed) DK (Completed) ES (Completed) NO (Completed) GB (Completed) CZ (Completed) HU (Completed) EE (Completed) GR (Prematurely Ended) PL (Completed) BG (Completed) RO (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-004903-22 | Sponsor Protocol Number: TOC110977 | Start Date*: 2016-12-12 |
Sponsor Name:GlaxoSmithKline Research & Development Ltd | ||
Full Title: A randomized, double-blind, multicenter, superiority Phase III study to assess the safety and efficacy of Topical Retapamulin Ointment 1%, applied twice daily versus Placebo Ointment in Adults and ... | ||
Medical condition: Secondarily-infected traumatic lesions (SITL), excluding those with abscesses. | ||
Disease: | ||
Population Age: Adolescents, Under 18, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2012-001644-21 | Sponsor Protocol Number: MEA115661 | Start Date*: 2013-06-24 |
Sponsor Name:GlaxoSmithKline Research & Development Ltd | ||
Full Title: MEA115661: A multi-centre, open-label, long-term safety study of mepolizumab in asthmatic subjects who participated in the MEA115588 or MEA115575 trials. | ||
Medical condition: Subjects with Severe Asthma | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) GB (Completed) DE (Completed) IT (Completed) ES (Completed) NL (Completed) CZ (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-001285-15 | Sponsor Protocol Number: KOIIM-2019-1 | Start Date*: 2019-06-28 |
Sponsor Name:University Medical Centre Ljubljana | ||
Full Title: Platelet inhibition with cangrelor in comatose survivors of out-of-hospital cardiac arrest undergoing primary percutaneous coronary intervention | ||
Medical condition: Comatose survivors of out-of-hospital cardiac arrest undergoing primary percutaneous coronary intervention | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-022584-35 | Sponsor Protocol Number: TUD-BRIDGE-046 | Start Date*: 2011-11-25 | |||||||||||
Sponsor Name:Dresden Universtity of Technology | |||||||||||||
Full Title: Clofarabine salvage therapy in patients with relapsed or refractory AML The BRIDGE Trial | |||||||||||||
Medical condition: Patients with AML >40 years of age with untreated relapse or refractory disease after a minimum of one standard induction therapy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003075-35 | Sponsor Protocol Number: CTT116855 | Start Date*: 2014-07-24 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: A phase III, 52 week, randomized, double-blind, 3-arm parallel group study, comparing the efficacy, safety and tolerability of the fixed dose triple combination fluticasone furoate/ umeclidinium/vi... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) FI (Completed) PL (Completed) SE (Completed) DE (Completed) AT (Completed) CZ (Completed) BE (Completed) DK (Completed) ES (Completed) NO (Completed) RO (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003647-34 | Sponsor Protocol Number: AMLSG23-14/Palbo-AL-1 | Start Date*: 2015-05-19 |
Sponsor Name:University Hospital Ulm | ||
Full Title: Phase Ib/IIa study of palbociclib in MLL-rearranged acute leukemias | ||
Medical condition: Acute myeloid leukemia Acute lymphoblastic leukemia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-009256-20 | Sponsor Protocol Number: OMB110928 | Start Date*: 2009-12-23 |
Sponsor Name:GlaxoSmithKline Research and Development Limited | ||
Full Title: Ofatumumab versus Rituximab Salvage Chemoimmunotherapy followed by ASCT in Relapsed or Refractory DLBCL | ||
Medical condition: Diffuse Large B-Cell Lymphoma (DLBCL) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) BE (Completed) SE (Prematurely Ended) IE (Prematurely Ended) GB (Prematurely Ended) ES (Prematurely Ended) CZ (Prematurely Ended) FI (Prematurely Ended) DK (Prematurely Ended) HU (Completed) PL (Prematurely Ended) DE (Prematurely Ended) AT (Completed) EE (Completed) GR (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2015-004885-27 | Sponsor Protocol Number: FFU109045 | Start Date*: 2016-12-12 |
Sponsor Name:GlaxoSmithKline Research & Development Ltd | ||
Full Title: A Comparison of Fluticasone Furoate Nasal Spray versus Oral Fexofenadine in the Treatment of Seasonal Allergic Rhinitis | ||
Medical condition: Seasonal allergic rhinitis (SAR) | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2020-000483-27 | Sponsor Protocol Number: CCT38473 | Start Date*: 2020-11-19 |
Sponsor Name:St. Joseph’s Healthcare, McMaster University | ||
Full Title: Re-Evaluating the Inhibition of Stress Erosions: Gastrointestinal Bleeding Prophylaxis in ICU | ||
Medical condition: critical illness requiring mechanical ventilation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2011-004438-32 | Sponsor Protocol Number: MOT115816 | Start Date*: 2012-04-25 | |||||||||||
Sponsor Name:GlaxoSmithKline Research and Development Limited | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, parallel group, dose ranging study to assess the effect of repeat doses of GSK962040 on the pharmacokinetics of levodopa in subjects with Parkinson’s... | |||||||||||||
Medical condition: Investigate the ability of the motilin receptor agonist GSK962040 to improve levodopa pharmacokinetics (PK) by enhancing GE via motilin receptor agonism. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) SE (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002361-32 | Sponsor Protocol Number: 201810 | Start Date*: 2016-04-05 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: A multi-center, randomized, double-blind, placebo controlled, parallel group study to compare cessation versus continuation of long-term mepolizumab treatment in patients with severe eosinophilic a... | |||||||||||||
Medical condition: severe eosinophilic asthma | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) NL (Completed) RO (Ongoing) FR (Completed) PL (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000090-32 | Sponsor Protocol Number: BBR-012CS01 | Start Date*: 2011-05-12 | |||||||||||
Sponsor Name:Bridge BioResearch Rights (Jersey) Ltd | |||||||||||||
Full Title: A Randomised, Double-Blind, Repeat-Dose, Placebo-Controlled Phase IIa Proof of Concept Study to Investigate the Safety and Efficacy of Oral BBR-012 in Combination With Standard Medical Care in Diab... | |||||||||||||
Medical condition: Complicated skin ulceration on the foot in patients with diabetes. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022510-11 | Sponsor Protocol Number: MEA114092 | Start Date*: 2011-02-23 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: A multicenter, open-label, dose ranging study to determine the pharmacokinetics and pharmacodynamics of mepolizumab administered intravenously or subcutaneously to adult asthmatic subjects with ele... | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) EE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001805-21 | Sponsor Protocol Number: RA486120 | Start Date*: 2020-05-15 |
Sponsor Name:University Hospital Coventry & Warwickshire | ||
Full Title: Prospective, Randomized, Parallel-Group, Open-Label Study to Evaluate the Efficacy and Safety of IMU-838, in Combination with Oseltamivir, in Adults with Coronavirus Disease COVID-19 | ||
Medical condition: Sars-Cov-2 | ||
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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