- Trials with a EudraCT protocol (438)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
438 result(s) found for: >.
Displaying page 5 of 22.
| EudraCT Number: 2008-006425-14 | Sponsor Protocol Number: PDX-014 | Start Date*: 2009-07-02 | |||||||||||
| Sponsor Name:Allos Therapeutics, Inc | |||||||||||||
| Full Title: Phase 1/2 Study of Pralatrexate in Female Patients with Previously-treated Advanced or Metastatic Breast Cancer | |||||||||||||
| Medical condition: Previously-treated Advanced or Metastatic Breast Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: FR (Ongoing) HU (Completed) CZ (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-002293-41 | Sponsor Protocol Number: AB12005 | Start Date*: 2015-07-02 | |||||||||||
| Sponsor Name:AB Science | |||||||||||||
| Full Title: A prospective, multicenter, double-randomised, double-blind, 2-parallel groups, phase 3 study to compare as first line therapy efficacy and safety of masitinib in combination with gemcitabine, to g... | |||||||||||||
| Medical condition: Non resectable locally advanced or metastatic pancreatic cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) BE (Completed) DE (Prohibited by CA) SK (Prohibited by CA) GR (Completed) GB (Temporarily Halted) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-003836-38 | Sponsor Protocol Number: MK-5172-077 | Start Date*: 2015-02-16 | |||||||||||
| Sponsor Name:Merck Corporation, Inc. | |||||||||||||
| Full Title: A Phase III, Open-Label Clinical Trial to Study the Efficacy and Safety of the Combination Regimen of MK-5172/MK-8742 versus Sofosbuvir/Pegylated Interferon/Ribavirin (PR) in Treatment-Naïve and PR... | |||||||||||||
| Medical condition: Hepatitis C | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) LT (Completed) ES (Completed) NO (Completed) HU (Completed) DK (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-000819-25 | Sponsor Protocol Number: DS102A-05-AH1 | Start Date*: 2019-01-31 | |||||||||||
| Sponsor Name:Afimmune | |||||||||||||
| Full Title: A Randomised, Double-Blind, Placebo-Controlled, Phase II Study to Assess the Efficacy and Safety of Orally Administered DS102 in Patients with Severe Acute Decompensated Alcoholic Hepatitis. | |||||||||||||
| Medical condition: Severe Acute Decompensated Alcoholic Hepatitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Prematurely Ended) FR (Prematurely Ended) DE (Prematurely Ended) LV (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-002349-80 | Sponsor Protocol Number: M13-583 | Start Date*: 2015-11-13 | |||||||||||
| Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
| Full Title: A Single-Arm, Open-Label Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Adults with Chronic Hepatitis C Virus Genotype 4, 5, or 6 Infection (ENDURANCE-4) | |||||||||||||
| Medical condition: Chronic Hepatitis C Virus Genotype 4, 5 or 6 Infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PT (Completed) BE (Completed) GB (Completed) ES (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-002203-15 | Sponsor Protocol Number: PregMet2 | Start Date*: 2012-08-08 | |||||||||||
| Sponsor Name:NTNU, Norwegian University of Science and Technology | |||||||||||||
| Full Title: Metformin treatment of pregnant PCOS women and prevention of late miscarriages and preterm birth The PregMet 2 Study | |||||||||||||
| Medical condition: Poly Cystic Ovarial Syndrome (PCOS) in pregnant women. PCOS should be diagnosed according to the Rotterdam Consensus criterias: - at least 2 out of 3 criterias 1.PCO in at least one ovary 2.Olig... | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: NO (Completed) SE (Completed) IS (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-015703-13 | Sponsor Protocol Number: InReTel | Start Date*: 2009-12-11 | ||||||||||||||||||||||||||
| Sponsor Name:Klinik für Innere Medizin II der Klinikum Chemnitz gGmbH | ||||||||||||||||||||||||||||
| Full Title: The influence of Telmisartan on insulin resistance and fatty liver in patients suffer from hypertension | ||||||||||||||||||||||||||||
| Medical condition: Influence of Telmisartan on insulin resistance, hypertension, non-alcoholic fatty liver | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2013-004688-30 | Sponsor Protocol Number: 15892A | Start Date*: 2014-05-19 | ||||||||||||||||
| Sponsor Name:H. Lundbeck A/S | ||||||||||||||||||
| Full Title: Interventional, open-label study of 18 mg Selincro® as needed use, in the treatment of patients with alcohol dependence in primary care | ||||||||||||||||||
| Medical condition: Alcohol Dependency | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) DE (Completed) ES (Completed) IT (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2008-001524-31 | Sponsor Protocol Number: URT-15/PBC | Start Date*: 2008-08-26 | |||||||||||
| Sponsor Name:Dr. Falk Pharma GmbH | |||||||||||||
| Full Title: Double-blind, double-dummy, randomized, crossover, multicentre phase IV clinical study comparing the effect of Ursofalk® 500 mg tablets od versus Ursofalk® 250 mg capsules od on liver enzyme parame... | |||||||||||||
| Medical condition: Treatment of primary biliary cirrhosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-001172-11 | Sponsor Protocol Number: MedOPP239 | Start Date*: 2020-03-10 | |||||||||||
| Sponsor Name:Medica Scientia Innovation Research (MedSIR) | |||||||||||||
| Full Title: A Multicenter, Open-Label, Single-ARm, PHase II Clinical Trial to Evaluate the Efficacy and Safety of INCMGA00012 in Advanced Penile SquamoUS Cell Carcinoma. ORPHEUS Phase II Study of the Efficacy ... | |||||||||||||
| Medical condition: Unresectable locally advanced or metastatic penile squamous cell carcinoma (PSqCC). | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: ES (Ongoing) IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-018982-43 | Sponsor Protocol Number: AB08025 | Start Date*: 2010-06-18 | ||||||||||||||||
| Sponsor Name:AB SCIENCE | ||||||||||||||||||
| Full Title: A prospective, multicenter, open-label, uncontrolled, two-parallel group, phase 1/2 study to evaluate safety and efficacy of masitinib at 9 mg/kg/day in monotherapy and in combination with dacarbaz... | ||||||||||||||||||
| Medical condition: Mélanome métastasé ou non-opérable stade 3 ou stade 4, ne portant pas de mutation dans le domaine juxta-membranaire de c-kit | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2010-018875-30 | Sponsor Protocol Number: BRD10/1-P | Start Date*: 2010-04-06 | |||||||||||
| Sponsor Name:CHU de Nantes | |||||||||||||
| Full Title: Comparaison de l’effet antisécrétoire d’une dose unique de rabeprazole 20 mg et d’omeprazole 20 mg chez des sujets obèses | |||||||||||||
| Medical condition: reflus gastro-oesophagien | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-005522-29 | Sponsor Protocol Number: M14-002 | Start Date*: 2013-04-17 | |||||||||||
| Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
| Full Title: A Randomized, Double-Blind, Controlled Study to Evaluate the Efficacy and Safety of the Combination of ABT-450/Ritonavir/ABT-267 (ABT-450/r/ABT-267) and ABT-333 With and Without Ribavirin (RBV) in ... | |||||||||||||
| Medical condition: Chronic Hepatitis C Infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-002925-36 | Sponsor Protocol Number: M14-867 | Start Date*: 2015-04-10 | |||||||||||
| Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
| Full Title: An Open-Label, Multicenter Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Co-Administration of ABT-493 and ABT-530 With and Without Ribavirin in Subjects with Chronic Hepatitis C V... | |||||||||||||
| Medical condition: Chronic Hepatitis C Virus (HCV) Infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-004603-35 | Sponsor Protocol Number: REACH | Start Date*: 2009-04-28 | |||||||||||||||||||||
| Sponsor Name:University of Heidelberg | |||||||||||||||||||||||
| Full Title: Radiotherapy (IMRT), Erbitux And Chemotherapy For Unresectable Carcinomas Of Head and Neck. REACH-Study | |||||||||||||||||||||||
| Medical condition: Histologically confirmed locally advanced (stage III or IV), non-metastatic squamous cell carcinoma of oro-, hypopharynx or larynx (T2-4, NX, M0). | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2011-006114-14 | Sponsor Protocol Number: 62326B1658 | Start Date*: 2012-04-17 |
| Sponsor Name:Research and Development department | ||
| Full Title: “Effects of testosterone on glycaemic control and other Cardiovascular Risk factors in Hypogonadal Men with uncontrolled Type 2 Diabetes: A randomized double – blinded placebo controlled add on tr... | ||
| Medical condition: Hypogonadism Type 2 Diabetes Cardiovascular risk | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-002056-25 | Sponsor Protocol Number: MK-8521-004 | Start Date*: 2016-09-06 |
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | ||
| Full Title: A Phase IIa, Multicenter, Placebo- and Active-controlled, Randomized, Double-Blind, Clinical Trial to Evaluate the Safety and Efficacy of MK-8521 Compared to Placebo in Subjects with Type 2 Diabete... | ||
| Medical condition: Type 2 Diabetes Mellitus | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-003192-22 | Sponsor Protocol Number: M16-126 | Start Date*: 2017-03-08 | |||||||||||
| Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
| Full Title: A Multicenter, Open-Label Study to Evaluate the Efficacy and Safety of Glecaprevir (GLE)/Pibrentasvir (PIB) in Adults with Chronic Hepatitis C Virus (HCV) Genotype 5 or 6 Infection. | |||||||||||||
| Medical condition: Chronic hepatitis C virus genotype 5 or 6 infection, cirrhosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-001182-41 | Sponsor Protocol Number: C0168X97 | Start Date*: 2007-03-27 | |||||||||||
| Sponsor Name:Ass.Prof. Petros Sfikakis | |||||||||||||
| Full Title: Infliximab for Diabetic Macular Edema Refractory to Laser Photocoagulation: a Randomized, Double-Masked, Placebo-Controlled, Cross-over, 32 Weeks Study | |||||||||||||
| Medical condition: Diabetic Macular Oedema | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-001192-29 | Sponsor Protocol Number: cv-08/025 | Start Date*: 2008-06-03 |
| Sponsor Name:Fundación Investigación y Desarrollo en el Area Cardiovascular | ||
| Full Title: “Evaluación mediante proteómica de biomarcadores proteicos asociados con el tratamiento con Eplerenona versus espironolactona en pacientes post-infarto agudo de miocardio, diabéticos con hipertensi... | ||
| Medical condition: Disfunción ventricular leve-moderada post-infarto agudo de miocardio en pacientes diabéticos con hipertensión arterial no controlada. Low-moderate ventricular dysfunction in post-acute coronary sy... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
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