- Trials with a EudraCT protocol (67)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
67 result(s) found for: Health care economics.
Displaying page 1 of 4.
EudraCT Number: 2006-001061-42 | Sponsor Protocol Number: 0881A3-405 | Start Date*: 2006-07-31 |
Sponsor Name:Wyeth Pharmaceuticals France, Wyeth Research Division | ||
Full Title: An open-label, multicentre, supplementary and extension study of Etanercept in subjects with Ankylosing Spondylitis (AS) | ||
Medical condition: Ankylosing spondylitis (AS). | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) SE (Completed) FI (Completed) DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-001993-52 | Sponsor Protocol Number: IMCOVAS | Start Date*: 2021-05-20 |
Sponsor Name:University of Antwerp | ||
Full Title: Assessment of the immunogenicity and safety of marketed vaccines for COVID-19 after regular schedule and adapted vaccine schedules and routes: BNT162b2 (Comirnaty®; Pfizer-BioNTech), mRNA-1273 Vacc... | ||
Medical condition: Coronavirus disease-19 (COVID-19) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002094-55 | Sponsor Protocol Number: 1861 | Start Date*: 2019-09-09 |
Sponsor Name:Universitair Ziekenhuis Brussel, Belgium | ||
Full Title: Safety and feasibility of S-Caine patch use in children under the age of three | ||
Medical condition: children under the age of three that are in possession of a central catheter and under permanent monitoring (healthy, or any condition) | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-002654-21 | Sponsor Protocol Number: S187.4.001 | Start Date*: 2005-08-08 |
Sponsor Name:Solvay Pharmaceuticals GmbH | ||
Full Title: A long-term health economics study of intraduodenal levodopa (Duodopa®) in routine care for patients with advanced idiopathic Parkinson’s disease with severe motor fluctuations and hyper-/dyskinesia. | ||
Medical condition: Treatment of advanced levodopa-responsive Parkinson’s disease with severe motor fluctuations and hyper-/dyskinesia when available combinations of Parkinson medicinal products have not given satisfa... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) NO (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-000505-72 | Sponsor Protocol Number: 2019-000505-72 | Start Date*: 2019-05-13 |
Sponsor Name:Transparency in Healthcare | ||
Full Title: Pragmatic trial baricitinib versus First biological in “Tight Control” Patients suffering from Rheumatoid Arthritis (PERFECT) | ||
Medical condition: Pragmatic trial baricitinib versus First biological in “Tight Control” Patients suffering from Rheumatoid Arthritis (PERFECT) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002259-11 | Sponsor Protocol Number: GRT-ZVO-2016-01 | Start Date*: 2016-10-10 |
Sponsor Name:GRUNENTHAL PHARMA S.A. | ||
Full Title: A multicenter, open-label, single-arm, Phase IIIb trial to evaluate the effectiveness, safety, tolerability, usability and health economics resource utilization of Zalviso® for management of acute ... | ||
Medical condition: Acute moderate to severe postoperative pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-001735-49 | Sponsor Protocol Number: CTU/2015/174 | Start Date*: 2019-07-01 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: Rivaroxaban versus warfarin for stroke patients with antiphospholipid syndrome, with or without SLE (RISAPS): a randomised, controlled, open-label, phase II/III, non-inferiority trial | |||||||||||||
Medical condition: Patients with stroke or other ischaemic brain injury who have antiphospholipid syndrome (APS), with or without systemic lupus erythematosus (SLE) | |||||||||||||
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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: 2017-003606-40 | Sponsor Protocol Number: SHP633-301 | Start Date*: 2018-05-28 | |||||||||||
Sponsor Name:Shire Human Genetic Therapies, Inc. | |||||||||||||
Full Title: A Randomized, Open-label, 24-Week Safety, Efficacy, and Pharmacokinetic Study of Teduglutide in Infants 4 to 12 Months of Age with Short Bowel Syndrome Who are Dependent on Parenteral Support Orig... | |||||||||||||
Medical condition: Short Bowel Syndrome (SBS) | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) FI (Completed) IT (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000863-17 | Sponsor Protocol Number: SHP633-303 | Start Date*: 2017-03-28 | |||||||||||
Sponsor Name:Shire Human Genetic Therapies, Inc. | |||||||||||||
Full Title: A Retrospective and Prospective, Open-label, Long-term Safety and Efficacy Study of Teduglutide in Pediatric Subjects with Short Bowel Syndrome Who Completed TED-C13-003 Original PIP P/238/2010 | |||||||||||||
Medical condition: short bowel syndrome | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000797-30 | Sponsor Protocol Number: SPI-IIT-002 | Start Date*: 2013-10-08 | |||||||||||||||||||||
Sponsor Name:Department of Medical Research, Odense University Hospital, Svendborg Hospital | |||||||||||||||||||||||
Full Title: Inhibition of aldosterone to diminish diffuse myocardial fibrosis in atrial fibrillation | |||||||||||||||||||||||
Medical condition: Paroxysmal and persistent atrial fibrillation | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-002093-12 | Sponsor Protocol Number: 1506-STBSG | Start Date*: 2017-07-04 | ||||||||||||||||
Sponsor Name:European Organisation for Research and Treatment of | ||||||||||||||||||
Full Title: A Phase II multicenter study comparing the efficacy of the oral angionenesis inhibitor nintedanib with the intravenous cytotoxis compound ifosfamide for treatment of patients with advanced metastat... | ||||||||||||||||||
Medical condition: Metastatic soft tissue sarcoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) GB (GB - no longer in EU/EEA) PL (Completed) NL (Completed) ES (Completed) LT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-000501-22 | Sponsor Protocol Number: SPON1189-13 | Start Date*: 2013-10-30 | |||||||||||
Sponsor Name:Cardiff Univeristy | |||||||||||||
Full Title: A national cancer research institute acute myeloid leukaemia working group pilot trial under the auspices of the cardiff experimental cancer medicine centre to establish the feasibility of combinin... | |||||||||||||
Medical condition: Acute Myeloid Leukaemia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000459-41 | Sponsor Protocol Number: PSMA-617-01 | Start Date*: 2018-09-04 | |||||||||||
Sponsor Name:Endocyte, Inc., A Novartis Company | |||||||||||||
Full Title: VISION: An international, prospective, open label, multicenter, randomized Phase 3 study of 177LU-PSMA-617 in the treatment of patients with progressive PSMA-positive metastatic castration-resistan... | |||||||||||||
Medical condition: PSMA-positive metastatic castration-resistant prostate cancer (mCRPC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) SE (Completed) FR (Completed) DK (Completed) NL (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003764-45 | Sponsor Protocol Number: UOL0727 | Start Date*: 2020-02-14 |
Sponsor Name:University of Leicester | ||
Full Title: Multicentre, open-label, randomised controlled trial of early surfactant therapy versus expectant management in late preterm and early term infants with respiratory distress. | ||
Medical condition: Respiratory distress in neonates born at 34 to 38+6 weeks of gestation | ||
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: 2005-002847-14 | Sponsor Protocol Number: CU 106 | Start Date*: 2005-12-16 | |||||||||||
Sponsor Name:Cardiff University | |||||||||||||
Full Title: AML16; A National Cancer Research Institute Trial in Acute Myeloid Leukaemia and High Risk Myelodysplastic Syndromes | |||||||||||||
Medical condition: Acute Myeloid Leukaemia and High Risk Myelodysplastic Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002195-90 | Sponsor Protocol Number: SPON1334-14 | Start Date*: Information not available in EudraCT | ||||||||||||||||
Sponsor Name:Cardiff University | ||||||||||||||||||
Full Title: Adults with acute myeloid leukaemia or high-risk myelodysplastic syndrome (AML19) | ||||||||||||||||||
Medical condition: Acute myeloid leukaemia High Risk Myelodysplastic Syndrome (trial arm for this patient group is now closed awaiting final analysis) | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001578-26 | Sponsor Protocol Number: TVT-Trial | Start Date*: 2012-11-07 | |||||||||||
Sponsor Name:St Olavs University Hospital [...] | |||||||||||||
Full Title: An international, multicentre, open randomised parallel group trial comparing a two step approach to cancer pain relief with the standard three step approach of the WHO analgesic ladder in patients... | |||||||||||||
Medical condition: Patients with cancer and cancer pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001310-42 | Sponsor Protocol Number: BL.13 | Start Date*: 2019-10-15 | ||||||||||||||||
Sponsor Name:Canadian Cancer Trials Group (CCTG) | ||||||||||||||||||
Full Title: A randomized phase II trial assessing trimodality therapy with or without adjuvant Durvalumab (MEDI4736) to treat patients with muscle-invasive bladder cáncer | ||||||||||||||||||
Medical condition: Muscle-invasive bladder cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003798-16 | Sponsor Protocol Number: 372-07 | Start Date*: 2008-10-13 |
Sponsor Name:Cardiff University | ||
Full Title: AML 17: A Programme of Treatment Development in Younger Patients with Acute Myeloid Leukaemia and High Risk Myelodysplastic Syndrome | ||
Medical condition: Acute Myeloid Leukaemia and High Risk Myelodysplastic Syndrome | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) DK (Completed) IE (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-001868-40 | Sponsor Protocol Number: SIEGE | Start Date*: 2013-11-05 | |||||||||||
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust | |||||||||||||
Full Title: Scheduling nab-paclItaxEl with GEmcitabine (SIEGE): Randomised phase II trial to investigate two different schedules of nab-paclitaxel (Abraxane) combined with gemcitabine as first line treatment f... | |||||||||||||
Medical condition: metastatic pancreatic adenocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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