- Trials with a EudraCT protocol (105)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
105 result(s) found for: Endothelin.
Displaying page 1 of 6.
EudraCT Number: 2005-001193-28 | Sponsor Protocol Number: AMB-320/321-E | Start Date*: 2005-11-08 |
Sponsor Name:Myogen, Inc | ||
Full Title: ARIES-320/321-E “A Long-Term Study of Ambrisentan in Pulmonary Arterial Hypertension Subjects Having Completed AMB-320 or AMB-321" | ||
Medical condition: Pulmonary Arterial Hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-003140-27 | Sponsor Protocol Number: V1.0/OPHT-020606 | Start Date*: 2006-07-25 |
Sponsor Name:Department of Clinical Pharmacology | ||
Full Title: Effects of non-specific Endothelin-A receptor blockade on ocular blood flow in patients with glaucoma | ||
Medical condition: patients with primary open angle glaucoma in comparision to a healthy control group. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-000812-29 | Sponsor Protocol Number: AMB 320 | Start Date*: 2005-09-21 | |||||||||||
Sponsor Name:Myogen, Inc. | |||||||||||||
Full Title: Ambrisentan in PAH - A Phase III, Randomised, Double- Blind, Placebo- Controlled, Multicenter, Efficacy Study of Ambrisentan in Subjects with Pulmonary Arterial Hypertension | |||||||||||||
Medical condition: Pulmonary Arterial Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) ES (Completed) AT (Completed) BE (Completed) IT (Completed) DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000848-14 | Sponsor Protocol Number: 38RC12.228 | Start Date*: 2014-07-23 |
Sponsor Name:Centre Hospitalier Universitaire de Grenoble | ||
Full Title: Endothelin and Ischemic optic Neuropathy study group | ||
Medical condition: Endothelin and Ischemic Optic Neuropathy study group | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000701-61 | Sponsor Protocol Number: BIRD-1 250705 | Start Date*: 2005-11-29 |
Sponsor Name:University College London | ||
Full Title: An open label trial of the dual specificity endothelin receptor antagonist bosentan in established scleroderma renal crisis | ||
Medical condition: Scleroderma renal crisis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-005679-33 | Sponsor Protocol Number: KKSH-042 | Start Date*: 2011-01-20 | ||||||||||||||||
Sponsor Name:Medizinische Fakultät der Martin-Luther-Universität Halle-Wittenberg | ||||||||||||||||||
Full Title: Influence of the selective endothelin receptor-blocker Ambrisetan on the portal pressure in patients with cirrhosis | ||||||||||||||||||
Medical condition: Portal hypertension and hepatic cirrhosis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003482-68 | Sponsor Protocol Number: BAY 63-2521/12934 | Start Date*: 2008-11-26 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: Randomized, double-blind, placebo-controlled, multi-centre, multi-national study to evaluate the efficacy and safety of oral BAY 63-2521 (1 mg, 1.5 mg, 2 mg, or 2.5 mg tid) in patients with symptom... | |||||||||||||
Medical condition: Pulmonary Arterial Hypertension (PAH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IE (Prematurely Ended) AT (Completed) ES (Completed) NL (Completed) FR (Completed) SE (Completed) GB (Completed) CZ (Completed) DK (Completed) BE (Completed) IT (Completed) PT (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023908-27 | Sponsor Protocol Number: AC-052-427 | Start Date*: 2011-03-16 | |||||||||||
Sponsor Name:Actelion Pharmaceuticals Nederland bv | |||||||||||||
Full Title: Effects of bosentan in a HOMogenEous population of SSc subjects with a predefined restriction of blood flow in the hands (HOME) | |||||||||||||
Medical condition: Digital Ulcera in Systemic Sclerodermia patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-014137-25 | Sponsor Protocol Number: VARDENAFIL&DIABETES | Start Date*: 2009-12-15 | |||||||||||
Sponsor Name:Unita` Operativa di Endocrinologia e Malattie del Metabolismo | |||||||||||||
Full Title: Monitoring of endothelial dysfunction during chronic administration of vardenafil in patients with type 2 diabetes mellitus: A longitudinal, randomised, placebo-controlled, double blind, phase II b... | |||||||||||||
Medical condition: patients affected by type 2 Diabetes mellitus and affected by mild or severe ED | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004533-21 | Sponsor Protocol Number: 03602 | Start Date*: 2010-06-25 | |||||||||||
Sponsor Name:ICIN | |||||||||||||
Full Title: The role of Bosentan in fontan patients: improvement of aerobic capacity | |||||||||||||
Medical condition: To study whether bosentan (endothelin receptor inhibitor) improves aerobic capacity (VO2max) and exercise performance in adult patients with a Fontan operation. | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004072-35 | Sponsor Protocol Number: 18-AOIP-01 | Start Date*: 2019-02-13 | |||||||||||
Sponsor Name:CHU de Nice | |||||||||||||
Full Title: Study of the value of early treatment with an endothelin inhibitor (Bosentan) in patients with sudden blindness secondary to giant cell arteritis | |||||||||||||
Medical condition: giant cell arteritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004391-36 | Sponsor Protocol Number: AC-052-402 | Start Date*: 2005-05-23 |
Sponsor Name:Actelion Pharmaceuticals Ltd. | ||
Full Title: A multicenter, open-label, single-arm safety study to investigate the effects of chronic TRACLEER® treatment on testicular function in male patients with pulmonary arterial hypertension | ||
Medical condition: Many endothelin receptor antagonists have profound effects on the histology and function of the testes in animals. These drugs have been shown to induce atrophy of the seminiferous tubules of the t... | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: HU (Completed) CZ (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-002686-21 | Sponsor Protocol Number: Bosentan1 | Start Date*: 2005-02-22 |
Sponsor Name:Dept of Dermatology | ||
Full Title: Efficacy of Endothelin 1 receptor antagonist Bosentan in secondary Raynauds Syndrom | ||
Medical condition: secondary Raynauds Syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-003133-33 | Sponsor Protocol Number: EMG-2006 | Start Date*: 2006-07-14 |
Sponsor Name:Hôpital Erasme | ||
Full Title: Etude des effets d’un antagoniste non spécifique de l’endothéline (le bosentan) sur l’activité orthosympathique et le chémoréflexe. | ||
Medical condition: healthy subjects obstructive sleep apnea (Bosentan is used in clinic in pulmonary hypertension) | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-002358-38 | Sponsor Protocol Number: RET-D-001 | Start Date*: 2015-04-28 | |||||||||||
Sponsor Name:Travere Therapeutics, Inc. | |||||||||||||
Full Title: PROTOCOL RET-D-001: EFFICACY AND SAFETY OF SPARSENTAN (RE-021), A DUAL ENDOTHELIN RECEPTOR AND ANGIOTENSIN RECEPTOR BLOCKER, IN PATIENTS WITH FOCAL SEGMENTAL GLOMERULOSCLEROSIS (FSGS): A RANDOMIZED... | |||||||||||||
Medical condition: FOCAL SEGMENTAL GLOMERULOSCLEROSIS (FSGS) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) IT (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001131-31 | Sponsor Protocol Number: FHC-1-2012 | Start Date*: 2012-06-14 | |||||||||||
Sponsor Name:Department of Medical Research | |||||||||||||
Full Title: Effekts of nebivolol on the nitric oxide system in patients with essentiel hypertension | |||||||||||||
Medical condition: Essential Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001412-38 | Sponsor Protocol Number: CQCC374X2201 | Start Date*: 2017-07-27 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A randomized, parallel-group, placebo-controlled subject and investigator blinded study to assess the safety, tolerability, pharmacokinetics and efficacy of QCC374 in the treatment of pulmonary art... | |||||||||||||
Medical condition: Pulmonary arterial hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002686-30 | Sponsor Protocol Number: CEP-AZ-SH-02 | Start Date*: 2009-04-15 | |||||||||||
Sponsor Name:Christie Hospital NHS Foundation Trust | |||||||||||||
Full Title: Assessment of the effects of the specific endothelin-A antagonist ZD4054 on prostate cancer biomarkers in patients with castrate-resistant metastatic disease | |||||||||||||
Medical condition: Prostate cancer | |||||||||||||
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Population Age: | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002623-42 | Sponsor Protocol Number: 66623 | Start Date*: 2019-02-18 | |||||||||||
Sponsor Name:Academic Medical Center | |||||||||||||
Full Title: Vasospastic angina treatment by Endothelin Receptor Antagonism; a proof of concept study | |||||||||||||
Medical condition: Vasospastic angina, i.e. epicardial vasospasm or microvascular coronary dysfunction. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005896-14 | Sponsor Protocol Number: Version 1.0 | Start Date*: 2006-02-20 |
Sponsor Name:Department of Clinical Pharmacology | ||
Full Title: Role of endothelin- and nitric oxide-system in the regulation of optic nerve head blood flow during changes in ocular perfusion pressure | ||
Medical condition: 18 healthy male volunteers Age 18-35 yrs., nonsmokers | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
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