- Trials with a EudraCT protocol (200)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
200 result(s) found for: N-terminal.
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EudraCT Number: 2014-002720-27 | Sponsor Protocol Number: 2014-002720-27 | Start Date*: 2014-12-04 |
Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | ||
Full Title: Simplification from Tenofovir plus Lamivudine or Emtricitabine plus Ritonavir-Boosted-Protease Inhibitor to Ritonavir-Boosted-Atazanavir plus Lamivudine in Virologically-Suppressed-HIV-Infected Adu... | ||
Medical condition: Chronic HIV infection. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-002960-27 | Sponsor Protocol Number: P-6708H | Start Date*: 2007-07-23 |
Sponsor Name:Pharma Nord ApS | ||
Full Title: Coenzyme Q10 as adjunctive treatment of chronic heart failure. A randomised double-blind multicenter trial with focus on Symptoms, Biomarker status (BNP) and long-term Outcome (hospitalisation/mort... | ||
Medical condition: Chronic heart failure for more than 6 weeks, in NYHA class III or IV. Age>18 years; males and females. Optimal medical treatment of heart failure according to the investigators opinion. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-001502-28 | Sponsor Protocol Number: PRED-AID | Start Date*: 2019-02-11 | |||||||||||
Sponsor Name:Imperial College London | |||||||||||||
Full Title: Safety and Efficacy of Prednisolone in Adrenal Insufficiency Disease (PRED-AID Study) | |||||||||||||
Medical condition: Adrenal insufficiency | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002207-15 | Sponsor Protocol Number: Cardiorete | Start Date*: 2011-12-27 |
Sponsor Name:FONDAZIONE DEL PIEMONTE PER L'ONCOLOGIA IRCC DI CANDIOLO | ||
Full Title: A prospective study with beta-blockers and ACE-inhibitors in patients operable breast cancer experiencing mild cardiac toxicity during treatment with anthracycline and/or trastuzumab | ||
Medical condition: patients experiencing mild cardiotoxicity during treatment with anthracycline and/or trastuzumab for operable breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-004633-41 | Sponsor Protocol Number: CS 82-000-04 | Start Date*: 2007-12-04 |
Sponsor Name:TransPharma Medical | ||
Full Title: A Multicenter, Randomized, Parallel Study to Assess the Clinical Efficacy, Safety, and Tolerability of ViaDerm-hPTH (1-34) (Double-Blinded for 2 Different Dosages) in Comparison to Subcutaneous Inj... | ||
Medical condition: The population for this study is post-menopausal, osteoporosis-treatment naïve women and patients with osteopenia, 55 years of age to 85 years of age, inclusive, with a lumbar vertebral BMD T-sco... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: HU (Completed) CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004398-76 | Sponsor Protocol Number: gjnh/mccormick/01 | Start Date*: 2006-03-22 |
Sponsor Name:Golden Jubilee National Hospital | ||
Full Title: A comparison of Myocardial Protection Using Preconditioning with Sevoflurane Against High Thoracic Epidural Analgesia for CABG Surgery | ||
Medical condition: Ischaemic heart disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2009-018125-70 | Sponsor Protocol Number: ENM-EA-016 | Start Date*: 2011-04-06 |
Sponsor Name:Medizinische Universität Graz | ||
Full Title: Styrian Vitamin D Hypertension Trial: A randomized, double-blind, placebo controlled trial to study the effects of vitamin D supplementation on systolic blood pressure in vitamin D deficient hypert... | ||
Medical condition: Patients with arterial hypertension and vitamin D deficiency | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-002007-38 | Sponsor Protocol Number: CLTP001A12201E1 | Start Date*: 2023-03-01 | |||||||||||
Sponsor Name:Novartis Farmacéutica, S.A. | |||||||||||||
Full Title: An open-label extension study to investigate efficacy, safety and tolerability of LTP001 in participants with pulmonary arterial hypertension | |||||||||||||
Medical condition: Pulmonary arterial hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002864-30 | Sponsor Protocol Number: NL73019.018.20 | Start Date*: 2020-07-29 |
Sponsor Name:Amsterdam UMC, location AMC | ||
Full Title: Sulodexide for chronic heart failure: a proof of concept, randomized, placebo-controlled study | ||
Medical condition: Chronic heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
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: 2017-004072-59 | Sponsor Protocol Number: 1245-0167 | Start Date*: 2018-04-03 |
Sponsor Name:Boehringer-Ingelheim España, S.A. | ||
Full Title: A phase III randomised, double-blind trial to evaluate the effect of 12 weeks treatment of once daily EMPagliflozin 10 mg compared with placebo on ExeRcise ability and heart failure symptoms, In pa... | ||
Medical condition: Chronic Heart Failure with preserved Ejection Fraction (HFpEF) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) GR (Completed) PT (Completed) PL (Completed) SE (Completed) NO (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-005999-13 | Sponsor Protocol Number: D8180C00034 | Start Date*: 2008-02-21 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A Phase II, Randomised, Open-label, Pilot Study to Evaluate the Safety and the Effects on Bone Resorption of AZD0530 in Patients with Prostate Cancer or Breast Cancer with Metastatic Bone Disease ... | ||
Medical condition: Prostate Cancer or Breast Cancer with Metastatic Bone Disease Cáncer de próstata o de mama con metástasis óseas | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) GB (Completed) SE (Completed) PT (Completed) DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-005724-10 | Sponsor Protocol Number: SPIHF-201 | Start Date*: 2016-06-07 | |||||||||||
Sponsor Name:Stealth BioTherapeutics Inc. | |||||||||||||
Full Title: A Phase 2 Randomized, Double-Blinded, Placebo-Controlled Study to Evaluate the Effects of Multiple Subcutaneous Injections of Elamipretide on Left Ventricular Function in Subjects with Stable Heart... | |||||||||||||
Medical condition: Stable Heart Failure with Reduced Ejection Fraction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001666-40 | Sponsor Protocol Number: CZOL446H2202E1 | Start Date*: 2005-02-01 |
Sponsor Name:Novartis Pharma AG | ||
Full Title: An international, multicenter, randomized, open-label, safety and efficacy trial of intravenous zoledronic acid administered either once or twice yearly in children with severe osteogenesis imperfe... | ||
Medical condition: Osteogenesis Imperfecta | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: HU (Prematurely Ended) GB (Completed) BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-000667-40 | Sponsor Protocol Number: APD811-003 | Start Date*: 2015-04-23 | |||||||||||
Sponsor Name:Arena Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, Double-blind, Parallel-group, Placebo-controlled Phase 2 Trial of APD811, an Oral IP Receptor Agonist, in Patients with Pulmonary Arterial Hypertension | |||||||||||||
Medical condition: Pulmonary Arterial Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) HU (Completed) ES (Completed) PL (Completed) RO (Ongoing) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000788-26 | Sponsor Protocol Number: 3/085/11 | Start Date*: 2012-06-18 |
Sponsor Name: [...] | ||
Full Title: The Effects of Inorganic Nitrite on cardiac and skeletal muscle: Physiology, Pharmacology and Therapeutic Potential in patients with Chronic Heart Failure | ||
Medical condition: Chronic heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-001285-15 | Sponsor Protocol Number: IIBSP-DEN-2012-24 | Start Date*: 2012-10-05 |
Sponsor Name:Institut de Recerca Hospital Sant Pau | ||
Full Title: Ensayo clínico aleatorizado, doble ciego, de grupos paralelos, controlado con placebo para la valoración de la eficacia del denosumab subcutáneo para la disminución de la resorción periprotésica en... | ||
Medical condition: Periprosthetic bone mineral density Masa ósea periprotésica | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-001147-31 | Sponsor Protocol Number: 140481 | Start Date*: 2013-06-06 |
Sponsor Name:Aarhus University Hospital, Department of Cardiology | ||
Full Title: Aortic Valve Stenosis and Myocardial Efficiency – a Prognostic Marker and a Target for Intervention? | ||
Medical condition: Aortic stenosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-004864-54 | Sponsor Protocol Number: BCBe/04/Neb-Car/082 | Start Date*: 2005-09-12 |
Sponsor Name:Berlin-Chemie Menarini | ||
Full Title: COMPARISON OF THE EFFECTS OF COMBINED RATE- AND RHYTHM-CONTROL TREATMENT WITH NEBIVOLOL AND ELECTRIC CARDIOVERSION TO RATE-CONTROL TREATMENT WITH NEBIVOLOL ALONE ON CLINICAL AND ECHOCARDIOGRAPHIC P... | ||
Medical condition: PATIENTS WITH HYPERTENSION AND LEFT-VENTRICULAR DYSFUNCTION INDUCED BY TACHYCARDIA | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-002037-11 | Sponsor Protocol Number: IIISAS | Start Date*: 2019-10-10 | |||||||||||
Sponsor Name:Oslo University Hospital | |||||||||||||
Full Title: Intravenous Iron supplement for Iron deficiency in patients with Severe Aortic Stenosis | |||||||||||||
Medical condition: Iron deficiency, aortic stenosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Ongoing) | |||||||||||||
Trial results: (No results available) |
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