- Trials with a EudraCT protocol (116)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
116 result(s) found for: Idiopathic Pulmonary Arterial Hypertension.
Displaying page 2 of 6.
| EudraCT Number: 2014-000091-25 | Sponsor Protocol Number: 2014GU001B | Start Date*: 2014-09-01 | ||||||||||||||||
| Sponsor Name:Royal Brompton and Harefield NHS Foundation Trust | ||||||||||||||||||
| Full Title: A single-centre, placebo-controlled, double-blinded, randomized, cross-over study of Iloprost (Ventavis®) in patients with Eisenmenger syndrome | ||||||||||||||||||
| Medical condition: Pulmonary Arterial Hypertension Eisenmenger syndrome | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2008-003572-21 | Sponsor Protocol Number: A7331009 | Start Date*: 2009-11-19 | |||||||||||
| Sponsor Name:Pfizer Ltd,Ramsgate Road,Sandwich,Kent CT13 9NJ | |||||||||||||
| Full Title: A PHASE 2A, RANDOMIZED, DOUBLE BLIND, PLACEBO-CONTROLLED, PARALLEL GROUP STUDY INVESTIGATING THE DOSE-RESPONSE OF PF-00489791 ON ACUTE HEMODYNAMICS IN SUBJECTS WITH IDIOPATHIC AND FAMILIAL PULMONAR... | |||||||||||||
| Medical condition: Pulmonary arterial hypertension. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Prematurely Ended) BE (Completed) DE (Prematurely Ended) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-001967-70 | Sponsor Protocol Number: AC-052-367 | Start Date*: 2005-10-13 |
| Sponsor Name:Actelion Pharmaceuticals Ltd. | ||
| Full Title: An open-label, long-term, safety, and tolerability extension study using the pediatric formulation of bosentan in the treatment of children with idiopathic or familial pulmonary arterial hypertensi... | ||
| Medical condition: Idiopathic or familial pulmonary arterial hypertension | ||
| Disease: | ||
| Population Age: Children, Under 18 | Gender: Male, Female | |
| Trial protocol: GB (Completed) DE (Completed) IT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-011013-24 | Sponsor Protocol Number: AC-063A302 | Start Date*: 2009-06-03 | |||||||||||
| Sponsor Name:Actelion Pharmaceuticals Ltd. | |||||||||||||
| Full Title: A Multicenter, Double-blind, Randomized Study comparing the Safety and Tolerability of Iloprost inhalation solution delivered by I-neb utilizing Power disc-15 and Power disc-6 in Patients with Symp... | |||||||||||||
| Medical condition: Indication: Symptomatic Pulmonary Arterial Hypertension | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-004971-42 | Sponsor Protocol Number: RVT-1201-2002 | Start Date*: 2021-10-26 | |||||||||||
| Sponsor Name:Altavant Sciences GmbH | |||||||||||||
| Full Title: A Phase 2b, Dose-Ranging, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study of Rodatristat Ethyl in Patients with Pulmonary Arterial Hypertension | |||||||||||||
| Medical condition: Pulmonary Arterial Hypertension (PAH) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) LV (Prematurely Ended) FR (Completed) BE (Completed) CZ (Prematurely Ended) PL (Prematurely Ended) IT (Prematurely Ended) BG (Prematurely Ended) ES (Ongoing) AT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-000137-31 | Sponsor Protocol Number: 2017-2019 | Start Date*: 2017-12-19 | ||||||||||||||||
| Sponsor Name:VU University Medical Center | ||||||||||||||||||
| Full Title: Pulmonary Hypertension REversal in Clusters of Patients With Identical Pathobiological Substrates. 6-Mercaptopurine Proof-of-Concept Trial | ||||||||||||||||||
| Medical condition: Pulmonary arterial hypertension | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2014-002590-10 | Sponsor Protocol Number: P130906 | Start Date*: 2016-02-11 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: Effect of bronchodilators on effort induced dyspnoea in patients suffering lung hypertension | |||||||||||||
| Medical condition: Idiopathic or heritable patients with pulmonary arterial hypertension (PAH). | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-021572-29 | Sponsor Protocol Number: AMB114588 | Start Date*: 2010-11-23 | |||||||||||||||||||||||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development, Ltd | |||||||||||||||||||||||||||||||||
| Full Title: An open-label, long term extension study for treatment of pulmonary arterial hypertension in paediatric patients aged 8 years up to 18 years who have participated in AMB112529 and in whom continued... | |||||||||||||||||||||||||||||||||
| Medical condition: Pulmonary Arterial Hypertension | |||||||||||||||||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: GR (Prematurely Ended) DE (Completed) NL (Ongoing) ES (Completed) HU (Completed) IT (Completed) FR (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2012-003921-13 | Sponsor Protocol Number: 12/0368 | Start Date*: 2013-06-07 | |||||||||||
| Sponsor Name:University College London | |||||||||||||
| Full Title: COMbination therapy for PulmonAry hypertension using RacEcadotril (COMPARE). | |||||||||||||
| Medical condition: Pulmonary hypertension | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-024585-22 | Sponsor Protocol Number: WILK3 | Start Date*: 2011-03-25 | |||||||||||
| Sponsor Name:Imperial College Academic Healthsciences Centre | |||||||||||||
| Full Title: What is the effect of intravenous iron supplementation on cardiopulmonary haemodynamics, exercise capacity and quality of life in patients with IPAH and iron deficiency? | |||||||||||||
| Medical condition: Idiopathic or familial pulmonary arterial hypertension | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-020424-21 | Sponsor Protocol Number: bbbipah.1 | Start Date*: 2011-01-10 | |||||||||||
| Sponsor Name:VU medical center | |||||||||||||
| Full Title: Betablocker Therapy in Pulmonary Arterial Hypertension | |||||||||||||
| Medical condition: Idiopathic pulmonal arterial hypertension | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-004815-29 | Sponsor Protocol Number: ULA03 | Start Date*: 2021-08-04 | |||||||||||
| Sponsor Name:Cardiorentis AG | |||||||||||||
| Full Title: Open-label, dose escalation study of ularitide for the investigation of hemodynamic effects in patients with pulmonary arterial hypertension (UPAH) | |||||||||||||
| 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: 2006-000801-50 | Sponsor Protocol Number: TDE-PH-302 | Start Date*: 2007-02-19 | |||||||||||
| Sponsor Name:United Therapeutics Corporation | |||||||||||||
| Full Title: A 12-Week, International, Multicenter, Double-Blind, Randomized, Placebo-Controlled Comparison of the Efficacy and Safety of Oral UT-15C Sustained Release Tablets in Subjects with Pulmonary Arteria... | |||||||||||||
| Medical condition: Idiopathic or Familial pulmonary arterial hypertension (PAH), including PAH associated with: 1) Appetite suppressant/toxin use, or 2) Repaired congenital systemic-to-pulmonary shunts (repaired ≥... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) FR (Completed) BE (Completed) NL (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-003928-37 | Sponsor Protocol Number: BAY63-2521/12916 | Start Date*: 2008-07-14 | |||||||||||
| Sponsor Name:Bayer AG | |||||||||||||
| Full Title: A multicenter, non-randomized, non-blinded, non-controlled study to investigate the impact of multiple doses of BAY 63-2521 on safety, tolerability, pharmacokinetics and pharmacodynamics in patient... | |||||||||||||
| Medical condition: Patients with interstitial lung disease associated pulmonary hypertension | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-002440-14 | Sponsor Protocol Number: AC-055-302 | Start Date*: 2008-05-15 | |||||||||||
| Sponsor Name:Actelion Pharmaceuticals Ltd. | |||||||||||||
| Full Title: A multicenter, double-blind, randomized, placebo-controlled, parallel group, event-driven, Phase III study to assess the effects of ACT-064992 on morbidity and mortality in patients with symptomati... | |||||||||||||
| Medical condition: To assess the effects of ACT-064992 on morbidity and mortality in patients with symptomatic pulmonary arterial hypertension | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) BE (Completed) DE (Completed) NL (Completed) FR (Completed) FI (Completed) SE (Completed) AT (Completed) DK (Completed) SK (Completed) PT (Prematurely Ended) IT (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-019547-19 | Sponsor Protocol Number: AMB112529 | Start Date*: 2010-07-16 | |||||||||||||||||||||||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development, Ltd | |||||||||||||||||||||||||||||||||
| Full Title: A randomized, open label study comparing safety and efficacy parameters for a high and a low dose of ambrisentan (adjusted for body weight) for the treatment of pulmonary arterial hypertension in ... | |||||||||||||||||||||||||||||||||
| Medical condition: Pulmonary Arterial Hypertension | |||||||||||||||||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: GR (Prematurely Ended) NL (Completed) HU (Completed) DE (Completed) ES (Completed) FR (Completed) IT (Completed) Outside EU/EEA | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2009-012057-38 | Sponsor Protocol Number: CQTI571A2301 | Start Date*: 2009-08-13 | |||||||||||
| Sponsor Name:Novartis Pharma Services AG | |||||||||||||
| Full Title: A 24-week randomized placebo-controlled, double-blind multi-center clinical trial evaluating the efficacy and safety of oral QTI571 as an add-on therapy in the treatment of severe pulmonary arteria... | |||||||||||||
| Medical condition: Pulmonary arterial hypertension (PAH) patients who have a PVR ≥800 dynes.sec.cm-5 despite treatment with two or more specific PAH therapies | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) AT (Completed) ES (Completed) FR (Completed) SE (Completed) BE (Completed) IT (Completed) NL (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-003978-41 | Sponsor Protocol Number: A1481298 | Start Date*: 2016-10-13 | |||||||||||
| Sponsor Name:Pfizer, Inc. | |||||||||||||
| Full Title: A Phase 3, Multi-center, Open label Study To Investigate Safety, Efficacy, And Tolerability Of Sildenafil Citrate In Pediatric Patients With Pulmonary Arterial Hypertension | |||||||||||||
| Medical condition: Pulmonary arterial hypertension | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-003462-14 | Sponsor Protocol Number: AC-055-310 | Start Date*: 2013-12-10 | |||||||||||
| Sponsor Name:ACTELION Pharmaceuticals Ltd. | |||||||||||||
| Full Title: A multi-center, open-label, single-arm, Phase 3b study of macitentan in patients with pulmonary arterial hypertension to psychometrically validate the French, Italian and Spanish versions of the PA... | |||||||||||||
| Medical condition: Pulmonary arterial hypertension | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-014246-29 | Sponsor Protocol Number: BPS-MR-PAH-203 | Start Date*: 2010-02-01 | |||||||||||
| Sponsor Name:Lung Rx | |||||||||||||
| Full Title: A 12-week, double-blind, international, multicenter, dose-response study of the safety and efficacy of Beraprost Sodium Modified Release (BPS-MR) in patients with pulmonary arterial hypertension (PAH) | |||||||||||||
| Medical condition: Pulmonary Arterial Hypertension | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (Completed) BE (Prematurely Ended) DE (Completed) CZ (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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