- Trials with a EudraCT protocol (12)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
12 result(s) found for: Zofenopril.
Displaying page 1 of 1.
EudraCT Number: 2004-001862-42 | Sponsor Protocol Number: MeBN/02/Zof-AMI/001 | Start Date*: 2005-02-17 |
Sponsor Name:Clinical Research Facilities | ||
Full Title: A multicenter, double-blind, randomized 2x2 factorial design study to compare the efficacy of early (<6 hours) versus late (24-48 hours) ACE-inhibition and to compare the efficacy of Zofenopril an... | ||
Medical condition: Study population: Subjects undergoing a primary percutaneous coronary intervention (PCI) to be performed within 6 hours after the onset of symptoms of a first acute anterior myocardial infarction ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-002340-23 | Sponsor Protocol Number: MEIN/19/ZoNe-HYP/001 | Start Date*: 2021-04-20 | |||||||||||
Sponsor Name:MENARINI INTERNATIONAL OPERATIONS LUXEMBOURG SA | |||||||||||||
Full Title: Open-label, multicenter, multinational, interventional clinical trial to assess effectiveness and safety of the extemporaneous combination of nebivolol and zofenopril calcium in grade 1 to 2 hypert... | |||||||||||||
Medical condition: Grade 1 and 2 hypertension | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001150-88 | Sponsor Protocol Number: MEN/03/ZOF-CHF/001 | Start Date*: 2005-05-06 | |||||||||||
Sponsor Name:Menarini International Operation Luxembourg -SA | |||||||||||||
Full Title: Comparison between zofenopril and ramipril in combination with ASA on the extent of cardiovascular risk in patients with systolic left ventricular dysfunction after acute myocardial infarction (SMI... | |||||||||||||
Medical condition: Systolic left ventricular dysfunction after AMI | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012993-10 | Sponsor Protocol Number: MEN/09/ZOF-IPE/001 | Start Date*: 2009-09-24 | |||||||||||
Sponsor Name:A. MENARINI I.F.R. | |||||||||||||
Full Title: EFFICACY AND SAFETY OF ZOFENOPRIL+HYDROCHLOROTHIAZIDE COMBINATION VS. IRBESARTAN+HYDROCHLOROTHIAZIDE COMBINATION IN METABOLIC SYNDROME PATIENTS WITH ESSENTIAL HYPERTENSION NOT CONTROLLED BY PREVIOU... | |||||||||||||
Medical condition: PATIENTS affected by METABOLIC SYNDROME WITH ESSENTIAL HYPERTENSION NOT CONTROLLED BY PREVIOUS MONOTHERAPY | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002439-33 | Sponsor Protocol Number: MeIn/08/ZOF+HCTZ-HYP/001 | Start Date*: 2008-06-26 | |||||||||||
Sponsor Name:MENARINI INTERNATIONAL OPERATIONS LUXEMBOURG S.A. | |||||||||||||
Full Title: EFFICACY AND SAFETY OF ZOFENOPRIL + HYDROCHLOROTHIAZIDE COMBINATION VS IRBESARTAN + HYDROCHLOROTHIAZIDE COMBINATION IN ESSENTIAL HYPERTENSIVE PATIENTS NOT CONTROLLED BY PREVIOUS MONOTHERAPY | |||||||||||||
Medical condition: Patients with essential hypertension and with at least one additional cardiovascular risk factor, not controlled by a previous monotherapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) LT (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021988-32 | Sponsor Protocol Number: LUMI/10/ZOF- HYP/001 | Start Date*: 2010-09-27 | |||||||||||
Sponsor Name:LUSOFARMACO | |||||||||||||
Full Title: A multicentre, multinational, randomised, double-blind, pilot, ascending dose for non responder, parallel group study on the therapeutic efficacy and safety of o.d. Zofenopril 30 mg plus HCTZ 12.5 ... | |||||||||||||
Medical condition: elderly subjects (age > 65 years) affected by Isolated Systolic Hypertension | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007681-30 | Sponsor Protocol Number: LUMI/08/ZOF-001 | Start Date*: 2009-02-06 | |||||||||||
Sponsor Name:LUSOFARMACO | |||||||||||||
Full Title: EFFICACY AND SAFETY OF ZOFENOPRIL + HYDROCHLOROTHIAZIDE COMBINATION VS. IRBESARTAN + HYDROCHLOROTHIAZIDE COMBINATION IN ESSENTIAL HYPERTENSIVE PATIENTS NOT CONTROLLED BY PREVIOUS MONOTHERAPY | |||||||||||||
Medical condition: Essential hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000745-40 | Sponsor Protocol Number: MEIN/20/ZoAm-Hyp/001 | Start Date*: 2022-01-03 | |||||||||||
Sponsor Name:MENARINI INTERNATIONAL OPERATIONS LUXEMBOURG SA | |||||||||||||
Full Title: Interventional clinical trial to assess efficacy and safety of the extemporaneous combination of Zofenopril calcium and amlodipine in grade 1-2 hypertensive patients versus each monotherapy | |||||||||||||
Medical condition: Grade 1-2 hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002077-23 | Sponsor Protocol Number: MeIn/03/Olm-Hyp/001 | Start Date*: 2005-08-24 |
Sponsor Name:MENARINI INTERNATIONAL OPERATIONS LUXEMBOURG S.A. | ||
Full Title: Efficacy and safety of Olmesartan medoxomil in elderly patients with mild to moderate hypertension | ||
Medical condition: Male or female outpatients, aged 65-89 years, with mild to moderate essential hypertension (sDBP>=90mmHg and sSBP>=140mmHg) | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: IE (Completed) AT (Completed) DE (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-015834-31 | Sponsor Protocol Number: CLCZ696B2314 | Start Date*: 2010-01-01 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A multicenter, randomized, double-blind, parallel group, active-controlled study to evaluate the efficacy and safety of LCZ696 compared to enalapril on morbidity and mortality in patients with chro... | |||||||||||||
Medical condition: Chronic Heart Failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) IS (Completed) GB (Completed) ES (Prematurely Ended) DE (Completed) HU (Completed) NL (Prematurely Ended) SE (Completed) IT (Prematurely Ended) RO (Completed) SK (Completed) FI (Completed) FR (Completed) DK (Completed) BE (Completed) CZ (Completed) LT (Completed) EE (Completed) LV (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004632-35 | Sponsor Protocol Number: CLCZ696BDE01 | Start Date*: 2016-05-04 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A randomized, double-blind, active-controlled study to assess the effect of LCZ696 compared with enalapril to improve exercise capacity in patients with heart failure with reduced ejection fraction... | |||||||||||||
Medical condition: chronic heart failure and reduced ejection fraction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000239-34 | Sponsor Protocol Number: PONTIACII | Start Date*: 2015-12-30 |
Sponsor Name:Medizinische Universität Wien | ||
Full Title: NT-proBNP Selected PreventiOn of cardiac eveNts in a populaTion of dIabetic patients without A history of Cardiac disease; a prospective randomized trial | ||
Medical condition: The purpose of this study is to evaluate the effect of high dose Renin-Angiotensin System (RAS)-antagonists and beta-blocker treatment for the primary prevention of cardiac events in a population o... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) NL (Ongoing) GB (GB - no longer in EU/EEA) ES (Ongoing) HU (Completed) | ||
Trial results: (No results available) |
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