- Trials with a EudraCT protocol (52)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
52 result(s) found for: Beta rhythm.
Displaying page 3 of 3.
EudraCT Number: 2015-002168-17 | Sponsor Protocol Number: BAY94-8862/16275 | Start Date*: 2015-12-09 | |||||||||||||||||||||||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||||||||||||||||||||||
Full Title: A multicenter, randomized, double-blind, double-dummy, parallel-group, active-controlled study to evaluate the efficacy and safety of finerenone compared to eplerenone on morbidity and mortality in... | |||||||||||||||||||||||||||||||||
Medical condition: Subjects with chronic heart failure and reduced ejection fraction after recent heart failure decompensation and additional risk factors, either type 2 diabetes mellitus or chronic kidney disease or... | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: SE (Prematurely Ended) DK (Prematurely Ended) IE (Prematurely Ended) CZ (Prematurely Ended) DE (Prematurely Ended) FI (Prematurely Ended) GB (Prematurely Ended) AT (Prematurely Ended) HU (Prematurely Ended) NL (Prematurely Ended) PT (Prematurely Ended) ES (Prematurely Ended) LT (Prematurely Ended) BG (Prematurely Ended) PL (Prematurely Ended) GR (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-002239-11 | Sponsor Protocol Number: MYK-491-003 | Start Date*: 2019-04-18 |
Sponsor Name:MyoKardia Inc. | ||
Full Title: Randomized, Double-blind, Placebo-controlled, Two-Part, Adaptive Design Study of Safety, Tolerability, Preliminary Pharmacokinetics, and Pharmacodynamics of Single and Multiple Ascending Oral Doses... | ||
Medical condition: Heart Failure with Reduced Ejection Fraction | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) GB (Completed) SE (Completed) NL (Ongoing) PL (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-014940-12 | Sponsor Protocol Number: CL2-44121-006 | Start Date*: 2010-03-11 | |||||||||||||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||||||||||||
Full Title: Evaluation of the anti-arrhythmic effects of 3 oral dosages of S 44121 versus placebo in patients with chronic heart failure and left ventricular systolic dysfunction at risk for ventricular arrhyt... | |||||||||||||||||||||||
Medical condition: Chronic Heart Failure and left ventricular systolic dysfunction at risk for ventricular arrhythmia | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Completed) HU (Completed) SK (Completed) ES (Completed) PT (Completed) GB (Completed) CZ (Completed) DE (Completed) BE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-004450-21 | Sponsor Protocol Number: EMR200136-570 | Start Date*: 2014-02-07 | |||||||||||
Sponsor Name:Merck Serono S.p.A. | |||||||||||||
Full Title: Multicenter, open-label, 12 weeks, phaseIV pRospectivE randomized study aimed at evaLuating whether sc IFN beta 1a (Rebif®) administered In the morning may affEct the severity of Flu-like syndrom... | |||||||||||||
Medical condition: relapsing multiple sclerosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005302-26 | Sponsor Protocol Number: DW.0701.005.2020P | Start Date*: 2023-01-05 | |||||||||||
Sponsor Name:John Paul II Hospital | |||||||||||||
Full Title: The effect of sacubitril/valsartan versus ramipril on left ventricular function and remodeling in patients with ischemic heart failure with mid-range ejection fraction | |||||||||||||
Medical condition: heart failure with moderately reduced ejection fraction (HFmrEF) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005989-34 | Sponsor Protocol Number: 034B20 | Start Date*: 2022-08-31 | |||||||||||
Sponsor Name:Aphaia Pharma AG | |||||||||||||
Full Title: A Phase II, randomized, double-blind, placebo-controlled, parallel-group proof-of-concept study to evaluate efficacy and safety of distal jejunal-release dextrose (Aphaia technology, AT) in obese s... | |||||||||||||
Medical condition: Obesity with/without associated endocrine and/or metabolic conditions and/or hypertension and/or NASH and/or NAFL with/without fibrosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000641-13 | Sponsor Protocol Number: BIO89-100-221 | Start Date*: 2020-09-30 | |||||||||||
Sponsor Name:89bio, Inc. | |||||||||||||
Full Title: A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study to Explore the Efficacy and Safety of BIO89-100 in Subjects with Severe Hypertriglyceridemia | |||||||||||||
Medical condition: Severe Hypertriglyceridemia (SHTG) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) CZ (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005048-17 | Sponsor Protocol Number: VRP080415 | Start Date*: 2009-01-27 | ||||||||||||||||
Sponsor Name:Verona Pharma Plc | ||||||||||||||||||
Full Title: A Combined Clinical Phase I/IIa Study of the Safety and Efficacy of Nebulised RPL554 in Healthy Subjects, Allergic Asthmatics, and Allergic Rhinitics | ||||||||||||||||||
Medical condition: Allergic Asthma and Allergic Rhinitis | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002429-39 | Sponsor Protocol Number: Leodor2017 | Start Date*: 2017-10-27 |
Sponsor Name:Medical University Innsbruck | ||
Full Title: REPETITIVE LEVOSIMENDAN INFUSIONS FOR PATIENTS WITH ADVANCED CHRONIC HEART FAILURE | ||
Medical condition: Advanced chronic heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) DE (Completed) HU (Completed) SI (Completed) FI (Completed) DK (Prematurely Ended) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-002681-39 | Sponsor Protocol Number: PHI113747 | Start Date*: 2013-12-20 | |||||||||||
Sponsor Name:GlaxoSmithKline, S.A. | |||||||||||||
Full Title: A 24-week, Phase 2B, randomized, active-controlled, parallel group, multi-center study to evaluate the safety and efficacy of GSK1278863 in subjects with anemia associated with chronic kidney disea... | |||||||||||||
Medical condition: Anemia associated with chronic kidney disease. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) SE (Completed) GB (Completed) CZ (Completed) HU (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004825-14 | Sponsor Protocol Number: D1680C00016 | Start Date*: 2016-05-04 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A 24-Week, Multicenter, Randomized, Double-blind, Parallel Group, Placebo-controlled Study to Investigate the Effects of Saxagliptin, Saxagliptin Combined with Dapagliflozin, and Sitagliptin in Pat... | |||||||||||||
Medical condition: Patients with type 2 diabetes mellitus and heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) HU (Completed) BG (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016378-34 | Sponsor Protocol Number: MI-CP204 | Start Date*: 2010-06-30 | |||||||||||||||||||||
Sponsor Name:MedImmune LLC | |||||||||||||||||||||||
Full Title: An Open Label, Phase 1/2 Study of MEDI-551, a Humanized Monoclonal Antibody Directed Against CD19, in Adult Subjects With Relapsed or Refractory Advanced B-Cell Malignancies | |||||||||||||||||||||||
Medical condition: Relapsed or refractory advanced B-cell malignancies: chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), B-cell non-Hodgkin’s lymphoma (NHL) (subtypes: follicular lymphoma (FL)... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BE (Completed) FR (Completed) | |||||||||||||||||||||||
Trial results: View results |
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