- Trials with a EudraCT protocol (575)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
575 result(s) found for: Add On Therapy.
Displaying page 1 of 29.
EudraCT Number: 2011-000739-97 | Sponsor Protocol Number: HIC | Start Date*: 2011-05-05 |
Sponsor Name:Med. Univ. Wien | ||
Full Title: Prospective, randomized, controlled, open-label study evaluating quality of life in patients with advanced malignant tumors with and without “add-on” homeopathy | ||
Medical condition: Homeopathic remedies as add on therapie in cancer | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-000815-15 | Sponsor Protocol Number: HLS14/01 | Start Date*: 2015-07-22 |
Sponsor Name:Azienda Ospedaliera, Polo Universitario Luigi Sacco, Milano | ||
Full Title: Effects of a late add-on therapy of pegylated interferon (peg-IFNA) to ongoing nucleos(t)ide analogs (NUCs) in patients with chronic hepatitis B (CHB). | ||
Medical condition: Chronic hepatitis B | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-001143-46 | Sponsor Protocol Number: CLAF237ADE08 | Start Date*: 2012-07-10 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A randomized open-label study to compare safety and efficacy of vildagliptin versus NPH insulin add-on to glimepiride in patients with type 2 diabetes mellitus that do not reach adequate glycemic c... | |||||||||||||
Medical condition: type-2 diabetes mellitus that do not reach adequate glycemic control on their current sulfonylurea monotherapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000542-20 | Sponsor Protocol Number: CLAF237A2338 | Start Date*: 2004-07-16 | |||||||||||
Sponsor Name:NOVARTIS FARMA | |||||||||||||
Full Title: A Multicenter, Double-Blind, Randomized, Active Controlled Study to Compare the Effect of 52 Weeks Treatment with LAF237 50 mg bid to Gliclazide up to 320 mg Daily as Add-On Therapy in Patients wit... | |||||||||||||
Medical condition: treatment of type 2 diabetes in combination therapy with other anti-diabetic oral drugs | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) SK (Completed) ES (Completed) DK (Completed) CZ (Completed) HU (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001546-32 | Sponsor Protocol Number: CLAF237A2305 | Start Date*: 2004-09-07 |
Sponsor Name:Novartis Finland Oy | ||
Full Title: A multicenter, double-blind, randomized, parallel-group study to compare the effect of 24 weeks treatment with LAF237 (50 mg qd or bid) to placebo as add-on therapy to glimepiride in patients with ... | ||
Medical condition: Patients with type 2 diabetes | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) LT (Completed) SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-003235-31 | Sponsor Protocol Number: Prof. Franz Weidinger | Start Date*: 2005-01-31 |
Sponsor Name:Div. of Cardiology, Innsbruck Medical University | ||
Full Title: Effect of pravastatin or fluvastatin and add-on valsartan on inflammatory markers and peripheral endothelial function in patients with acute coronary syndrome | ||
Medical condition: Acute coronary syndrome; patients with NSTEMI | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2004-004559-21 | Sponsor Protocol Number: CLAF237A2308 | Start Date*: 2005-03-04 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A Multicenter, Randomized, Double-Blind, Active Controlled Study to Compare the Long-Term Effect (up to 5 Years) of Treatment with LAF237 50 mg bid to Glimepiride up to 6 mg Daily as Add-On Therapy... | ||
Medical condition: Type II Diabetes | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) DK (Prematurely Ended) GB (Completed) LT (Completed) EE (Completed) LV (Completed) IT (Prematurely Ended) DE (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-001989-42 | Sponsor Protocol Number: TEA-Stroke | Start Date*: 2013-08-02 | |||||||||||
Sponsor Name:Boris Modrau | |||||||||||||
Full Title: Theophylline Effect in Acute Ischemic Stroke Trial | |||||||||||||
Medical condition: Acute ischemic stroke patients eligible for standard intravenous recombinant tissue plasminogen activator (rtPA) thrombolytic therapy with magnet resonance imaging (MRI)-proved infarction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015979-27 | Sponsor Protocol Number: TRX2 | Start Date*: 2010-02-25 | |||||||||||
Sponsor Name:Activartis Biotech GmbH | |||||||||||||
Full Title: First line standard therapy of glioblastoma multiforme with or without add-on treatment with Trivax, an anti-tumour immune therapy based on tumour-lysate charged dendritic cells | |||||||||||||
Medical condition: Patients older than 3 years of age with newly diagnosed Glioblastoma Multiforme (GBM) undergoing brain surgery for removal of at least 70% of tumour mass and receiving subsequently standard radiati... | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021097-11 | Sponsor Protocol Number: CLAF237A23152 | Start Date*: 2010-11-22 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A multi-center, randomized, double-blind placebo controlled study to evaluate the efficacy and safety of 24 weeks treatment with vildagliptin 50 mg bid as add-on therapy to metformin plus glimepiri... | ||
Medical condition: Type II Diabetes Mellitus | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) GB (Completed) HU (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-003127-38 | Sponsor Protocol Number: NL71001.029.19 | Start Date*: 2020-04-09 |
Sponsor Name:VUmc Neurology Department | ||
Full Title: Efficacy of add-on high dose simvastatin on markers for disease progression in MS patients treated with ocrelizumab and natalizumab (SIMSON), a phase II clinical trial. | ||
Medical condition: Multiple sclerosis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001664-38 | Sponsor Protocol Number: FFA-MAE | Start Date*: 2019-10-02 | |||||||||||
Sponsor Name:University Hospital Schleswig-Holstein (UKSH) | |||||||||||||
Full Title: A proof of concept and assessment of maximal effect study with low dose Fenfluramine as add-on therapy in Myoclonic Astatic Epilepsy (Doose-Syndrome) | |||||||||||||
Medical condition: Childhood epilepsy: Myoclonic Astatic Epilepsy (Doose-Syndrome) | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Restarted) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004059-53 | Sponsor Protocol Number: 16-OBE2109-009 | Start Date*: 2017-05-25 | |||||||||||
Sponsor Name:ObsEva SA | |||||||||||||
Full Title: A Phase 3, multicentre, randomized, double-blind, placebo controlled study investigating the efficacy and safety of daily oral administration of OBE2109 alone and in combination with add-back thera... | |||||||||||||
Medical condition: Treatment of heavy menstrual bleeding associated with uterine fibroids. | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: HU (Completed) LV (Completed) CZ (Completed) BG (Completed) PL (Completed) LT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018580-42 | Sponsor Protocol Number: PXL008-002 | Start Date*: 2010-06-11 | |||||||||||
Sponsor Name:Poxel | |||||||||||||
Full Title: Randomized, double-blind, placebo-controlled, parallel-group study of the safety and efficacy of imeglimin or placebo add-on therapy in type 2 diabetic subjects not adequately controlled by metform... | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000541-12 | Sponsor Protocol Number: AC-058B302 | Start Date*: 2016-11-15 | |||||||||||
Sponsor Name:Actelion Pharmaceuticals Ltd. | |||||||||||||
Full Title: Multicenter, randomized, double-blind, parallel-group, add-on, superiority study to compare the efficacy and safety of ponesimod to placebo in subjects with active relapsing multiple sclerosis who ... | |||||||||||||
Medical condition: Relapsing multiple sclerosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) PT (Completed) DK (Completed) HU (Completed) CZ (Completed) AT (Completed) ES (Prematurely Ended) GR (Completed) BG (Completed) FR (Completed) PL (Completed) FI (Completed) BE (Prematurely Ended) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002812-10 | Sponsor Protocol Number: PADD-ON | Start Date*: 2012-01-03 | |||||||||||
Sponsor Name:University Medical Center of the Johannes Gutenberg University Mainz | |||||||||||||
Full Title: A prospective, randomised, open-label phase IIb clinical trial assessing the effect of pegylated Interferon alfa-2a (Pegasys®) 180 µg once weekly for 48 weeks in addition to an ongoing nucelos(t)id... | |||||||||||||
Medical condition: Patients with chronic HBeAg-negative hepatitis B with a stable oral antiviral treatment (not containing telbivudine) and a fully suppressed viral load for at least 12 months (below limit of detecti... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001099-11 | Sponsor Protocol Number: CIGE025A2425 | Start Date*: 2005-10-18 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, open label, parallel-group, international, multicenter study evaluating persistency of response to omalizumab during 32 weeks treatment given as add on to optimized asthma therapy in ... | |||||||||||||
Medical condition: Severe persistent allergic asthma | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) NO (Completed) IE (Completed) ES (Completed) DK (Completed) SE (Completed) DE (Completed) HU (Completed) PT (Not Authorised) IT (Completed) BE (Completed) GR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006239-11 | Sponsor Protocol Number: HBV 09-01 | Start Date*: 2009-05-15 | |||||||||||
Sponsor Name:Stichting Lever Onderzoek | |||||||||||||
Full Title: Augmenting response to entecavir using a temporary peginterferon alpha-2a add-on strategy for the treatment of HBeAg-positive chronic hepatitis B (ARES study) | |||||||||||||
Medical condition: Chronic hepatitis B virus infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003813-92 | Sponsor Protocol Number: EPT02/2016 | Start Date*: 2017-01-25 | |||||||||||
Sponsor Name:IBSA FARMACEUTICI ITALIA SRL | |||||||||||||
Full Title: Open clinical trial to evaluate the efficacy of intravesical instillation of hyaluronate added to early instillation of mitomycin vs early instillation of mitomycin in patients suffering from low r... | |||||||||||||
Medical condition: Low risk not muscle-infiltrating bladder neoplasia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-004253-22 | Sponsor Protocol Number: ALXN2040-PNH-303 | Start Date*: 2022-07-04 | |||||||||||
Sponsor Name:Alexion Pharmaceuticals Inc. | |||||||||||||
Full Title: A Long-term Extension (LTE) Study to Characterize the Safety and Efficacy of Danicopan as an Add-on Therapy to a Complement Component 5 Inhibitor (C5i) in Patients with Paroxysmal Nocturnal Hemoglo... | |||||||||||||
Medical condition: Patients with Paroxysmal Nocturnal Hemoglobinuria | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) IT (Ongoing) GR (Ongoing) PL (Ongoing) | |||||||||||||
Trial results: (No results available) |
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