- Trials with a EudraCT protocol (60)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
60 result(s) found for: Angiotensin II receptor type 1.
Displaying page 1 of 3.
| EudraCT Number: 2020-001172-15 | Sponsor Protocol Number: APN01-01-COVID19 | Start Date*: 2020-04-08 |
| Sponsor Name:APEIRON Biologics AG | ||
| Full Title: Recombinant human angiotensin-converting enzyme 2 (rhACE2) as a treat-ment for patients with COVID-19 | ||
| Medical condition: Severe COVID-19 POSITIVE hospitalized male or female, between 18 and ≤ 80 years of age | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) DK (Completed) AT (Completed) GB (GB - no longer in EU/EEA) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-012676-27 | Sponsor Protocol Number: FemExp-I | Start Date*: 2010-01-24 | ||||||||||||||||
| Sponsor Name:Wallenberg laboratory | ||||||||||||||||||
| Full Title: Femoral-Express-I | ||||||||||||||||||
| Medical condition: Peripheral artery disease. Patients due for by-pass surgery of lower extremity arteries. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: SE (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2006-003991-37 | Sponsor Protocol Number: AGO/2006/009 | Start Date*: 2006-12-13 | |||||||||||
| Sponsor Name:University Hospital Gent | |||||||||||||
| Full Title: Trial of beta blocker therapy (atenolol) vs. angiotensin II receptor blocker therapy (losartan) in individuals with Marfan syndrome | |||||||||||||
| Medical condition: Marfan syndrome | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-003262-17 | Sponsor Protocol Number: AG-1-2007. | Start Date*: 2008-08-13 |
| Sponsor Name:University Hospital Magdeburg | ||
| Full Title: Impact of irbesartan on oxidative stress and C-reactive protein levels in patients with persistent atrial fibrillation | ||
| Medical condition: Blocking the angiotensin II type 1 receptor reduces systemic levels of oxidative stress markers and adhesion molecules compared to placebo in patients with persistent/permanent atrial fibrillation. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-007881-45 | Sponsor Protocol Number: SPP100ANL02T | Start Date*: 2009-03-12 | ||||||||||||||||
| Sponsor Name:University Medical Center Groningen | ||||||||||||||||||
| Full Title: A double-blind, placebo-controlled, randomized trial investigating the safety and efficacy of Additive Renin Inhibition with Aliskiren on renal blood flow and Neurohormonal Activation in patients w... | ||||||||||||||||||
| Medical condition: Patients with chronic heart failure and reduced glomerular filtration rate. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2019-003175-19 | Sponsor Protocol Number: U1111-1206-7541 | Start Date*: 2019-11-28 | |||||||||||
| Sponsor Name:Steno Diabetes Center Copenhagen | |||||||||||||
| Full Title: Renal effects of treatment with Empagliflozin alone or in combination with Semaglutide in patients with type 2 diabetes and albuminuria - A double blinded, randomised, placebo controlled, parallel... | |||||||||||||
| Medical condition: Type 2 diabetes with renal complications | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-001191-12 | Sponsor Protocol Number: Salt og Cirrhose | Start Date*: 2005-07-06 |
| Sponsor Name:Odense Universitetshospital | ||
| Full Title: Forebyggelse af inkompenseret levercirrose med Losartan Et prospektivt randomiseret dobbeltblindet lantidsstudie | ||
| Medical condition: Alkoholisk levercirrose. Fibrosedannelse og senere cirrose i leveren efter en årrække med øget indtag/misbrug af alkohol. Komplikationer ses i form af inkomensation med ascites, oesofagusvaricer og... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-001190-25 | Sponsor Protocol Number: A6291015 | Start Date*: 2004-12-17 |
| Sponsor Name:Pfizer Ltd | ||
| Full Title: A Double-blind, Proof of Concept Trial of the Use of Pegvisomant to Reduce Urinary Albumin Excretion in Type 1 and Type 2 Diabetic Patients Treated with Angiotensin Convertase Inhibitors/Angiotensi... | ||
| Medical condition: Diabetic nephropathy DN (Diabetes mellitus (DM) type I and type II with renal manifestations). MedDRA classification code : 10061835, 10045236 and 10045250 (Version 7.0, Level LLT) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: LT (Completed) CZ (Completed) DE (Completed) GB (Completed) ES (Completed) DK (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-002878-50 | Sponsor Protocol Number: NN9535-4321 | Start Date*: 2019-04-02 | ||||||||||||||||
| Sponsor Name:Novo Nordisk A/S | ||||||||||||||||||
| Full Title: Effect of semaglutide versus placebo on the progression of renal impairment in subjects with type 2 diabetes and chronic kidney disease | ||||||||||||||||||
| Medical condition: Diabetes Mellitus, Type 2 Chronic kidney disease | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) HU (Completed) NL (Completed) SK (Completed) BG (Completed) DE (Completed) ES (Ongoing) FR (Completed) PL (Completed) BE (Completed) GR (Completed) IT (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2010-019798-13 | Sponsor Protocol Number: MB102-077 | Start Date*: 2011-03-04 | ||||||||||||||||
| Sponsor Name:Bristol Myers Squibb International Corporation | ||||||||||||||||||
| Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Phase 3 Trial to Evaluate the Safety and Efficacy of Dapagliflozin in Subjects with Type 2 Diabetes with Inadequately Co... | ||||||||||||||||||
| Medical condition: Type 2 diabetes with inadequate glycemic control and inadequately controlled hypertension | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) HU (Completed) DE (Completed) FI (Completed) DK (Completed) IE (Completed) CZ (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2011-005710-11 | Sponsor Protocol Number: SNOXE36C301 | Start Date*: 2012-02-15 | ||||||||||||||||
| Sponsor Name:NOXXON Pharma AG | ||||||||||||||||||
| Full Title: A phase IIa study to characterize the effects of CCL2 inhibition with the Spiegelmer® NOX-E36 in patients with type 2 diabetes mellitus and albuminuria. | ||||||||||||||||||
| Medical condition: diabetes mellitus type II and albuminuria | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) HU (Completed) PL (Completed) CZ (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2010-019797-32 | Sponsor Protocol Number: MB102-073 | Start Date*: 2010-09-30 | ||||||||||||||||
| Sponsor Name:Bristol Myers Squibb International Corporation | ||||||||||||||||||
| Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Phase 3 Trial to Evaluate the Safety and Efficacy of Dapagliflozin in Subjects with Type 2 Diabetes with inadequately c... | ||||||||||||||||||
| Medical condition: Men and women with type 2 diabetes, ages ≥ 18 to ≤ 89 years, who have type 2 diabetes with inadequately controlled hypertension. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: HU (Completed) DE (Completed) ES (Completed) CZ (Completed) FI (Completed) DK (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2005-000362-39 | Sponsor Protocol Number: CSPP100A2243 | Start Date*: 2005-06-22 |
| Sponsor Name:Novartis Pharma Services AG | ||
| Full Title: A randomized, double-blind, parallel-group, cross-over, 4-period, 4 treatment, within-subject placebo-controlled study to assess the renoprotective effect of renin inhibition with Aliskiren as an a... | ||
| Medical condition: Hypertension | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-003610-41 | Sponsor Protocol Number: CL2-78989-011 | Start Date*: 2015-03-20 | |||||||||||
| Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
| Full Title: Dose-response study of gevokizumab (S78989) 3mg, 10mg, 30mg or 60mg in patients with type 2 diabetes and diabetic kidney disease (DKD). A 66-week, international, multicenter, randomized, double-bli... | |||||||||||||
| Medical condition: Diabetic kidney disease in patients with type 2 diabetes | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Prematurely Ended) SK (Completed) BE (Completed) DE (Prematurely Ended) DK (Prematurely Ended) SE (Completed) ES (Completed) PT (Completed) PL (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-003962-14 | Sponsor Protocol Number: BLO K022 | Start Date*: 2004-12-16 |
| Sponsor Name:Takeda Pharma GmbH | ||
| Full Title: Candesartan "added" Treatment for Optimisation of Heart Failure (HF) Therapy - Effects on BNP and other HF associated Parameters. An open, non-controlled and multicentre trial | ||
| Medical condition: Heart failure | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-002676-24 | Sponsor Protocol Number: D1690C00023 | Start Date*: 2015-11-24 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: An exploratory Phase II/III, randomized, double-blind, placebo controlled, parallel design study to evaluate the efficacy, safety and pharmacodynamics of dapagliflozin and dapagliflozin in combinat... | |||||||||||||
| Medical condition: CKD3 patients with type 2 diabetes mellitus and albuminuria. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-005093-54 | Sponsor Protocol Number: CV202-010 | Start Date*: 2013-05-30 | |||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
| Full Title: A Double-Blind, Placebo-Controlled, Randomized, Twostage, Parallel-Group, Adaptive Design Phase 2a Study to Evaluate the Effects of BMS-813160 in Subjects with Type 2 Diabetes Mellitus and Diabetic... | |||||||||||||
| Medical condition: Diabetic kidney disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-003674-32 | Sponsor Protocol Number: 1.1:12-6-2015 | Start Date*: 2016-02-23 |
| Sponsor Name:Leiden University Medical Center | ||
| Full Title: The effect of Telmisartan on inflammatory processes in the vascular wall of abdominal aortic aneurysms. | ||
| Medical condition: Abdominal aortic aneurysm with an indication for elective open surgical repair. | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-003037-11 | Sponsor Protocol Number: 21839 | Start Date*: 2022-04-13 | |||||||||||
| Sponsor Name:Bayer AG | |||||||||||||
| Full Title: A parallel-group treatment, Phase 2, double-blind, three-arm study to assess efficacy and safety of finerenone plus empagliflozin compared with either finerenone or empagliflozin in participants wi... | |||||||||||||
| Medical condition: Chronic kidney disease in type 2 diabetes mellitus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Trial now transitioned) FR (Trial now transitioned) BE (Trial now transitioned) IT (Trial now transitioned) NL (Ongoing) DK (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-004545-34 | Sponsor Protocol Number: AT10001 | Start Date*: 2006-02-20 |
| Sponsor Name:Unit of Esophageal and Gastric Research Dep. of Molecular Medicine and Surgery Karolinska Institutet | ||
| Full Title: Can Angiotensin II type 1 Receptor Inhibitor Be Used to Lower the Amount of Lipase and Amylase Level after Endoscopic Retrograde Cholangio-Pancreatography? | ||
| Medical condition: The clinical diagnosis of acute pancreatitis is set by a combination of symptoms (abdominal pain) and increased blood levels of pancreatic enzymes (i.e. amylase and lipase). The most common complic... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: View results | ||
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