- Trials with a EudraCT protocol (6,032)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
6,032 result(s) found for: Medical therapy.
Displaying page 228 of 302.
EudraCT Number: 2014-004898-16 | Sponsor Protocol Number: V_1 | Start Date*: 2015-05-27 | |||||||||||
Sponsor Name:Medizinische Universität Wien | |||||||||||||
Full Title: A study to investigate (R)-11C-verapamil PET as a predictive biomarker for epilepsy surgery outcome | |||||||||||||
Medical condition: temporal lobe epilepsy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023324-25 | Sponsor Protocol Number: ABCSG32 | Start Date*: 2011-03-31 |
Sponsor Name:ABCSG (Austrian Breast & Colorectal Cancer Study Group) | ||
Full Title: Multicentre randomized phase II study of neoadjuvant trastuzumab plus docetaxel with and without bevacizumab and trastuzumab plus docetaxel plus non-pegylated liposome-encapsulated doxorubicin (NPL... | ||
Medical condition: HER2-positive, adenocarcinoma of the breast (except inflammatory breast cancer, T4d) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-005928-16 | Sponsor Protocol Number: FLT3502 | Start Date*: 2007-03-19 | |||||||||||
Sponsor Name:Mundipharma Research Ltd. | |||||||||||||
Full Title: An open, randomised, parallel group, multicentre study to compare the efficacy and safety of FlutiForm pMDI vs Seretide pMDI in paediatric subjects with mild to moderate persistent, reversible asthma. | |||||||||||||
Medical condition: Asthma bronchial | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) DE (Completed) FR (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002101-35 | Sponsor Protocol Number: HyperCarD2 | Start Date*: 2017-08-24 |
Sponsor Name:Sten Madsbad | ||
Full Title: THE ROLE OF HYPERGLYCEMIA, HYPERINSULINEMIA AND ELEVATED FREE FATTY ACIDS FOR CARDIAC FUNCTION IN PATIENTS WITH TYPE 2 DIABETES – THE HYPERCARD2 STUDY | ||
Medical condition: typé 2 diabetes | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-012200-98 | Sponsor Protocol Number: yCAN | Start Date*: 2011-01-21 | |||||||||||
Sponsor Name:University Medical Center Hamburg-Eppendorf | |||||||||||||
Full Title: Open-label, prospective, randomized, parallel group study investigating a CNI-low dose regimen with Sandimmun® Optoral and Certican® in comparison to standard immunosuppressive therapy in renal tra... | |||||||||||||
Medical condition: Maintenance outpatient renal transplant recipients at least 6 months post-transplantation, no longer than 8 years after transplantation with a creeping serum creatinine (as calculated by CAN-Slope®... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000085-32 | Sponsor Protocol Number: TG6006.01 | Start Date*: 2018-05-04 | |||||||||||
Sponsor Name:TRANSGENE SA | |||||||||||||
Full Title: A phase I/IIa trial to evaluate the safety and efficacy of the combination of the oncolytic immunotherapy Pexa-Vec with the PD-1 receptor blocking antibody nivolumab in the first-line treatment of ... | |||||||||||||
Medical condition: Hepatocellular carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007028-25 | Sponsor Protocol Number: ON/2008/2781 | Start Date*: 2010-08-17 | |||||||||||
Sponsor Name:University Hospitals Bristol NHS Foundation Trust | |||||||||||||
Full Title: A Randomised Controlled Trial to Determine the Effect of Decapeptyl on Reduction of Prostate Volume Pre-Radiotherapy Compared with Standard Therapy (Zoladex) | |||||||||||||
Medical condition: Enrolled patients will be those with a diagnosis of prostate cancer who require radiotherapy to the prostate, with medical castration by means of Luteneising Hormone Releasing Hormone analogue (LRH... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004526-33 | Sponsor Protocol Number: PDARCT1 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Royal College of Surgeons in Ireland | |||||||||||||
Full Title: A Randomised Controlled Trial of Early Targeted Patent Ductus Arteriosus Treatment Using a Risk Based Severity Score | |||||||||||||
Medical condition: Patent Ductus Arteriosus | |||||||||||||
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Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003219-77 | Sponsor Protocol Number: 2012-003219-77 | Start Date*: 2012-12-20 | |||||||||||
Sponsor Name:Copenhagen University Hospital, Rigshospitalet | |||||||||||||
Full Title: Effects on Exercise Hemodynamics of Vasopressin Blockade by Conivaptan Infusion in Heart Failure | |||||||||||||
Medical condition: Heart Failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000644-13 | Sponsor Protocol Number: 07/06 | Start Date*: 2006-08-04 | |||||||||||
Sponsor Name:I.T.M.O. - ITALIAN TRIALS IN MEDICAL ONCOLOGY | |||||||||||||
Full Title: Multicenter, randomized, controlled study to compare palonosetron plus dexamethasone before chemotherapy administration versus the same regimen with dexamethasone continuing on Days 2 and 3 in pre... | |||||||||||||
Medical condition: Solid tumours | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002105-22 | Sponsor Protocol Number: EVL-VHC-HVH.12 | Start Date*: 2012-08-17 | ||||||||||||||||
Sponsor Name:Dra Itxarone Bilbao. Servicio de cirugía hepatobiliopancreatica y trasplantes. HUVH | ||||||||||||||||||
Full Title: Personal monitoring of liver transplant patients infected with Hepatitis C Virus. Pilot study to compare the evolution of Hepatitis C by receiving immunosuppression with tacrolimus in combination w... | ||||||||||||||||||
Medical condition: Recurrence of hepatitis C post-liver transplantation in patients with hepatitic C. | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-000043-27 | Sponsor Protocol Number: 191622-105 | Start Date*: Information not available in EudraCT | ||||||||||||||||
Sponsor Name:Allergan Limited | ||||||||||||||||||
Full Title: BOTOX® Treatment in Pediatric Upper Limb Spasticity: Open-label Study | ||||||||||||||||||
Medical condition: Upper limb spasticity | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) PL (Completed) HU (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-000084-24 | Sponsor Protocol Number: 191622-112 | Start Date*: 2013-07-08 | ||||||||||||||||
Sponsor Name:Allergan Limited | ||||||||||||||||||
Full Title: BOTOX® Treatment of Pediatric Lower Limb Spasticity: Open-label Study | ||||||||||||||||||
Medical condition: Lower Limb Spasticity | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) PL (Completed) HU (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-004218-41 | Sponsor Protocol Number: GB27862 | Start Date*: 2012-06-19 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A Phase III, randomized, double-blind, placebo-controlled study to assess the efficacy and safety of LEBRIKIZUMAB in patients with uncontrolled asthma who are on inhaled corticosteroids and second ... | |||||||||||||
Medical condition: Uncontrolled asthma despite the use of an inhaled corticosteroid and a second controller medication. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) ES (Prematurely Ended) SK (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003712-20 | Sponsor Protocol Number: SPON1451-15 | Start Date*: 2016-09-05 | ||||||||||||||||
Sponsor Name:Cardiff University | ||||||||||||||||||
Full Title: A randomised, double blind, double-dummy, placebo controlled trial of inhaled treatment to establish the mechanisms of prematurity-associated airway obstruction and inflammation. | ||||||||||||||||||
Medical condition: prematurity-related airway obstruction and inflammation | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-004021-33 | Sponsor Protocol Number: ANB019-002 | Start Date*: 2018-05-04 | |||||||||||
Sponsor Name:AnaptysBio Inc. | |||||||||||||
Full Title: A Single Arm Multiple Dose Study to Assess the Efficacy and Safety of ANB019 in Subjects with Generalized Pustular Psoriasis | |||||||||||||
Medical condition: Generalized Pustular Psoriasis (GPP) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005192-89 | Sponsor Protocol Number: C1231001 | Start Date*: 2015-04-21 | |||||||||||
Sponsor Name:Hospira UK Ltd. | |||||||||||||
Full Title: Post-Marketing Observational Cohort Study of Patients with Inflammatory Bowel Disease (IBD) Treated with CT-P13 in Usual Clinical Practice (CONNECT-IBD) | |||||||||||||
Medical condition: Inflamatory Bowel Disease (IBD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000427-27 | Sponsor Protocol Number: VIPER-SHOCK | Start Date*: 2017-03-30 | |||||||||||
Sponsor Name:Section for Transfusion Medicine, Capitol Region Blood Bank | |||||||||||||
Full Title: Vasculopathic Injury and Plasma as Endothelial Rescue in septic shock (SHOCK) trial | |||||||||||||
Medical condition: Patients with septic shock admitted to the intensive care unit. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019964-36 | Sponsor Protocol Number: CL004_354 | Start Date*: 2010-08-26 | |||||||||||
Sponsor Name:ChemoCentryx, Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Phase 2 Study to Evaluate the Safety and Efficacy of CCX354-C in Subjects with Rheumatoid Arthritis Partially Responsive to Methotrexate Therapy | |||||||||||||
Medical condition: Rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) HU (Completed) CZ (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004944-23 | Sponsor Protocol Number: WFTL001 | Start Date*: 2012-03-01 | |||||||||||
Sponsor Name:Charité Universitätsmedizin | |||||||||||||
Full Title: | |||||||||||||
Medical condition: graft function adapted tacrolimus therapy after liver transplantation | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
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