- Trials with a EudraCT protocol (1,091)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,091 result(s) found for: alpha-.
Displaying page 8 of 55.
EudraCT Number: 2007-003718-32 | Sponsor Protocol Number: BAY79-4980/12781 | Start Date*: 2008-06-27 | ||||||||||||||||
Sponsor Name:Bayer HealthCare AG | ||||||||||||||||||
Full Title: Randomized, active-controlled, double-blind, parallel design study to evaluate the efficacy and safety of a once-a-week prophylaxis treatment with BAY 79-4980 compared to three times-per-week proph... | ||||||||||||||||||
Medical condition: Hemophilia A | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: DE (Completed) FR (Completed) NL (Completed) DK (Prematurely Ended) ES (Completed) BE (Completed) AT (Completed) GB (Completed) IT (Completed) NO (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-002360-28 | Sponsor Protocol Number: 104886 | Start Date*: 2005-09-13 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: An open, randomized phase I/II study to demonstrate the non inferiority in term of cellular mediated immune response between GlaxoSmithKline Biologicals influenza candidate vaccines containing vari... | ||
Medical condition: Immunisation against influenza disease in adults aged 18-40 years and elderly population aged over 65 years (>65 years) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-005605-36 | Sponsor Protocol Number: SCI-Ta1-NSCLC-CHEMOP2-001 | Start Date*: 2016-07-07 | |||||||||||
Sponsor Name:SCICLONE PHARMACEUTICALS ITALY S.R.L. | |||||||||||||
Full Title: Thymosin alpha 1 plus maintenance therapy with the Standard of Care (SoC) chemotherapy plus cisplatin (or carboplatin) in patients with metastatic Non-Small Cell Lung Cancer (NSCLC), EGFR wild type | |||||||||||||
Medical condition: metastatic Non-Small Cell Lung Cancer (NSCLC), EGFR wild type | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004173-32 | Sponsor Protocol Number: 1-10-72-164-15 | Start Date*: 2015-12-18 | |||||||||||
Sponsor Name:Department of Clinical Biochemestry, Aarhus University Hospital | |||||||||||||
Full Title: Personalized medicine: Administration of TNF-alpha inhibitor treatment due to serum concentration measuring. A randomized and investigator initiated study. | |||||||||||||
Medical condition: Rheumatic diseases | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003679-48 | Sponsor Protocol Number: CNTO1275AKS3001 | Start Date*: 2015-12-09 | |||||||||||
Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating the Efficacy and Safety of Ustekinumab in the Treatment of Anti-TNF alpha Naive Subjects With Active Radiograph... | |||||||||||||
Medical condition: Axial Spondyloarthritis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003129-40 | Sponsor Protocol Number: FARM125FKN | Start Date*: 2017-01-05 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA PISANA | |||||||||||||
Full Title: PHASE 4, MULTICENTER RANDOMISED STUDY, AIMED AT EVALUATING THE MAINTENANCE OF REMISSION AFTER 6, 12, 18 AND 24 MONTHS FROM SUSPENSION OF TNF-ALPHA THERAPIES (ADALIMUMAB, ETANERCEPT, INFLIXIMAB, CER... | |||||||||||||
Medical condition: RHEUMATOID ARTHRITIS (RA) PATIENTS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000120-40 | Sponsor Protocol Number: 2006/0606 | Start Date*: 2007-06-07 |
Sponsor Name:Centre Hospitalier Régional et Universitaire | ||
Full Title: Etude contrôlée comparative en double aveugle de l'effet d'un traitement par le fénofibrate sur l'expression des génes de l'homéostasie du cholestérol, de l'inflammation et de la prolifération cell... | ||
Medical condition: Patients présentant des lésions athérosclérosiques carotidiennes asymptomatiques diabétiques ou non diabétiques sous statines . | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-018531-17 | Sponsor Protocol Number: TRED012010 | Start Date*: 2010-06-25 |
Sponsor Name:Central Manchester University Hospitals NHS Foundation Trust | ||
Full Title: Effect of Tredaptive on serum lipoproteins, lipoproteins metabolism, oxidative stress and HDL antioxidant function. | ||
Medical condition: Hypercholesterolaemia. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-001426-24 | Sponsor Protocol Number: P02470 | Start Date*: 2004-11-23 |
Sponsor Name:Prof. Heinz Ludwig, MD, Wilhelminenspital, First Department of Medicine and Medical Oncology | ||
Full Title: Multicenter, open, randomized study for first-line treatment of multiple myeloma: thalidomide/dexamethasone vs. MP for induction therapy and thalidomide/Intron A vs. Intron A for maintenance therapy | ||
Medical condition: First line treatment of multiple myeloma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-001277-25 | Sponsor Protocol Number: ST1472-DM-03-004 | Start Date*: 2004-09-27 | |||||||||||
Sponsor Name:SIGMA-TAU | |||||||||||||
Full Title: A Phase III, Multicentre, Double Blinded Study in Patients with Chronic Hepatitis C who are Non-responders to prior PEGinterferon alpha + Ribavirin Therapy Comparing Treatment with Thymosin alpha 1... | |||||||||||||
Medical condition: Treatment of Patients with Chronic Hepatitis C who are Non-responders to a course with approved doses of PEGinterferon alpha + Ribavirin | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) DE (Ongoing) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001653-28 | Sponsor Protocol Number: 03/314 | Start Date*: Information not available in EudraCT |
Sponsor Name:The Leeds teaching Hospitals NHS trust | ||
Full Title: A comparison of the effects on prostaglandin synthesis and cytokine production of an olive-oil based lipid emulsion (Clinoloeic) with a soya based emulsion (Intralipid) in newborn infnats receiving... | ||
Medical condition: Prematurity Parenteral nutrition | ||
Disease: | ||
Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2015-003521-34 | Sponsor Protocol Number: CHUBX2015/14 | Start Date*: 2015-10-09 |
Sponsor Name:CHU de Bordeaux | ||
Full Title: Hypertrophic CARdiomyopathy symptom release by alpha stimulant MIDOdrine | ||
Medical condition: Hypertrophic cardiomyopathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001492-33 | Sponsor Protocol Number: CGE_2020_9 | Start Date*: 2020-04-10 |
Sponsor Name:Hôpital Fondation Adolphe de Rothschild | ||
Full Title: Interest in the administration of Dornase alpha aerosol in ARDS secondary to respiratory infection by the coronavirus SRASCoV-2 / COVID-19 | ||
Medical condition: Patients on mechanical ventilation, inpatient resuscitation for ARDS, secondary to COVID-19 infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-004756-38 | Sponsor Protocol Number: 2018-1201 | Start Date*: 2019-02-12 |
Sponsor Name:Institut de Cancérologie Lucien Neuwirth | ||
Full Title: Study of thromboelastography during tranexamic acid treatment in preventing bleeding in patients with haematological malignancies presenting severe thrombocytopenia (TTRAP-bleeding) | ||
Medical condition: Malignant hemopathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2022-003581-20 | Sponsor Protocol Number: ALPHA | Start Date*: 2023-03-21 |
Sponsor Name:Medical University Vienna | ||
Full Title: Albendazole pharmacokinetics in plasma, intra-cystic fluid, and cystic tissue of human cystic and alveolar echinococcosis | ||
Medical condition: Albendazole is an orally administered broad-spectrum anthelmintic Drug used in treatment of human alveolar and cystic echinococcosis. To date, data on albendazole and tissue pharmacokinetics are li... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001283-30 | Sponsor Protocol Number: SPK-3006-101 | Start Date*: 2020-06-16 | |||||||||||
Sponsor Name:Spark Therapeutics | |||||||||||||
Full Title: Phase 1/2, dose-escalation study to evaluate the safety, tolerability and efficacy of a single intravenous infusion of SPK-3006 in adults with late-onset Pompe disease | |||||||||||||
Medical condition: Pompe Disease (also known as glycogen storage disease type II) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) DE (Trial now transitioned) NL (Ongoing) DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004300-65 | Sponsor Protocol Number: AGO/2016/012 | Start Date*: 2017-09-26 |
Sponsor Name:Ghent University Hospital | ||
Full Title: Optimizing the Biologic Treatment Strategy in Rheumatoid Arthritis (RA) Patients that have failed a Tumor Necrosis Factor-alpha (TNFα) blocking Agent by immunoscintigraphy with Technetium-labeled C... | ||
Medical condition: rheumatoid arthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-002635-28 | Sponsor Protocol Number: OFT-Campos01-12 | Start Date*: 2013-04-19 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: ASSESSMENT OF THE EFFICACY OF SUBTENON NATURAL LEUCOCYTIC INTERFERON-α (IFNα) FOR THE TREATMENT OF DIABETIC MACULAR EDEMA (DME): A PILOT STUDY. | |||||||||||||
Medical condition: DIABETIC MACULAR EDEMA (DME) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001072-22 | Sponsor Protocol Number: T51/2015 | Start Date*: 2016-01-26 | |||||||||||
Sponsor Name:Turku University Hospital | |||||||||||||
Full Title: Clinical and virological efficacy of pegylated interferon alpha in the treatment of rhinovirus infection in patients with primary hypogammaglobulinemia: randomized controlled trial | |||||||||||||
Medical condition: Rhinovirus infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000212-34 | Sponsor Protocol Number: AG348-C-018 | Start Date*: 2021-10-11 | |||||||||||
Sponsor Name:Agios Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 3, Double-blind, Randomized, Placebo-Controlled, Multicenter Study Evaluating the Efficacy and Safety of Mitapivat in Subjects With Transfusion-Dependent Alpha- or Beta-Thalassemia (ENERGIZ... | |||||||||||||
Medical condition: Transfusion-Dependent Alpha- or Beta-Thalassemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) DK (Trial now transitioned) IT (Trial now transitioned) BG (Trial now transitioned) FR (Trial now transitioned) NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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