- Trials with a EudraCT protocol (31,642)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
31,642 result(s) found for: 0.
Displaying page 471 of 1,583.
EudraCT Number: 2010-022855-46 | Sponsor Protocol Number: EWALL-PH-02 | Start Date*: 2011-07-13 |
Sponsor Name:Dekan des Fachbereichs Medizin der Goethe Universität, represented by the Coordinating Investigator | ||
Full Title: AN OPEN LABEL PHASE II STUDY TO EVALUATE THE EFFICACY AND SAFETY OF INDUCTION AND CONSOLIDATION THERAPY WITH NILOTINIB IN COMBINATION WITH CHEMOTHERAPY IN PATIENTS AGED 55 YEARS AND OVER WITH PHIL... | ||
Medical condition: Philadelphia chromosome positive Acute Lymphoblastic Leukemia in elderly Patients (55 years and older) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) IT (Prematurely Ended) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-004977-10 | Sponsor Protocol Number: 08meInnereA_GALACTIC | Start Date*: 2013-07-25 | |||||||||||||||||||||
Sponsor Name:University Hospital Basel, Cardiology | |||||||||||||||||||||||
Full Title: Goal-directed Afterload Reduction in Acute Congestive Cardiac Decompensation Study | |||||||||||||||||||||||
Medical condition: - acute decompensated heart failure | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Prohibited by CA) BG (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-001559-20 | Sponsor Protocol Number: 95195608 | Start Date*: 2007-04-17 |
Sponsor Name:Cliniques Universitaires Saint-Luc | ||
Full Title: Steady-state pharmacokinetics of high dose acetaminophen inpost-op children. Rational use of N-acetyl cysteine for prevention of liver toxicity related to cumulative doses. | ||
Medical condition: Major surgery when the use of paracetamol is required for pain release | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: BE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-001294-18 | Sponsor Protocol Number: CS I-040302/01 | Start Date*: 2007-09-06 | |||||||||||
Sponsor Name:Kuros Biosurgery AG | |||||||||||||
Full Title: A phase 2 randomised, open-label, multi-centre ascending dose study of the efficacy, safety and tolerability of I-040302 versus control injection (bone marrow aspirate or steroids) in children and ... | |||||||||||||
Medical condition: Solitary Bone Cysts | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) CZ (Completed) SK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002150-31 | Sponsor Protocol Number: 20090302 | Start Date*: 2012-08-29 | ||||||||||||||||
Sponsor Name:Amgen Inc | ||||||||||||||||||
Full Title: An Open-label, Single-dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Darbepoetin alfa in Paediatric Subjects From Birth to Less than 1 Year of Age With A... | ||||||||||||||||||
Medical condition: Anaemia due to chronic kidney disease | ||||||||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Prematurely Ended) HU (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-019057-17 | Sponsor Protocol Number: SPC3649-203 | Start Date*: 2010-07-13 |
Sponsor Name:Santaris Pharma A/S | ||
Full Title: A Phase 2a, Randomized, Double-Blind, Placebo-Controlled, Ascending Multiple-Dose Study to Assess Safety, Tolerability, Pharmacokinetics and Antiviral Activity of SPC3649 (miravirsen) Administered ... | ||
Medical condition: Patients infected with chronic hepatitis C | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) DE (Completed) SK (Completed) PL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-000305-35 | Sponsor Protocol Number: MKC-T1-102 | Start Date*: 2006-06-23 | |||||||||||
Sponsor Name:MannKind Corporation | |||||||||||||
Full Title: A Prospective, Multi-Center, Open-Label, Randomized, Controlled Clinical Trial Comparing the Efficacy and Safety in Subjects With Type 2 Diabetes Receiving Subcutaneous Basal Insulin and Prandial I... | |||||||||||||
Medical condition: Diabetes mellitus type II | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001975-15 | Sponsor Protocol Number: NL77514.078.21 | Start Date*: 2022-07-26 |
Sponsor Name: | ||
Full Title: The effect of extra hydration on kidney function during carboplatinpemetrexed-pembrolizumab in patients with advanced non-small cell lung cancer. | ||
Medical condition: Patient with advanced non-small cell lung cancer receiving treatment with carboplatin-pemetrexed-pembrolizumab. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002042-36 | Sponsor Protocol Number: CNTO148UCO2001 | Start Date*: 2014-07-10 | |||||||||||
Sponsor Name:Janssen Biologics B.V. | |||||||||||||
Full Title: A Phase 2a Open-label Study to Evaluate Prediction of Response to Golimumab Using a Transcriptomic Profile in Subjects with Moderately to Severely Active Ulcerative Colitis | |||||||||||||
Medical condition: Moderately to Severely Active Ulcerative Colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) HU (Completed) CZ (Completed) BG (Completed) PL (Completed) DE (Completed) NL (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003111-22 | Sponsor Protocol Number: V98_21 | Start Date*: 2014-11-06 | |||||||||||
Sponsor Name:GlaxoSmithKline Biologicals S.A. | |||||||||||||
Full Title: A Phase II, Randomized, Comparative, Observer-Blind, Multi-Center Study Evaluating the Safety and Immunogenicity of the Liquid Formulation of Group B Streptococcus Trivalent Vaccine and of the Lyop... | |||||||||||||
Medical condition: Healthy person immune response to Group B Streptococcus polysaccharide capsule antigens | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001245-32 | Sponsor Protocol Number: PGX-III-AP-002 | Start Date*: 2011-10-19 | |||||||||||
Sponsor Name:Forest Laboratories, Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind Trial of Apadenoson for the Detection of Myocardial Perfusion Defects Using Single-Photon Emission Computed Tomography (SPECT) Myocardial Perfusion Imaging (MPI) | |||||||||||||
Medical condition: Coronary Artery Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001308-40 | Sponsor Protocol Number: INHIXACOVID19 | Start Date*: 2020-05-04 | ||||||||||||||||
Sponsor Name:ALMA MATER STUDIORUM UNIVERSITà DI BOLOGNA | ||||||||||||||||||
Full Title: Intermediate dose enoxaparin in hospitalized patients with moderate-severe COVID-19: a pilot phase II single-arm study, INHIXACOVID19 | ||||||||||||||||||
Medical condition: Hospitalized adult patients with microbiologically confirmed moderate-severe COVID-19 infection | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002999-83 | Sponsor Protocol Number: UmUDURONORR1 | Start Date*: 2015-01-21 |
Sponsor Name:Johan Styrke | ||
Full Title: Ciprofloxacin vs Trimetoprim/Sulfametoxazol for transrectal prostate biopsy - a randomized double blind phaze IV multicentre clinical trial | ||
Medical condition: Prophylaxis of bacterial infektions of the prostate following transrectal prostate biopsy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: SE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001343-44 | Sponsor Protocol Number: IB-0319-002 | Start Date*: 2019-05-21 |
Sponsor Name:Instituto Bernabeu | ||
Full Title: Conventional ovarian stimulation vs. stimulation with single injection of Corifollitropin alfa in oocyte donors. Randomized clinical trial. Tail Studio | ||
Medical condition: Oocyte donation | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-003986-42 | Sponsor Protocol Number: Rifa1 | Start Date*: 2008-06-18 | |||||||||||
Sponsor Name:University Hospital of Tübingen | |||||||||||||
Full Title: Prospective, randomised, placebo controlled, double blind monocenter trial for the prophylactic treatment of diarrhoea with rifaximin for travellers to South- and Southeast-Asia | |||||||||||||
Medical condition: diarrhoea of travellers to South- and Southeast-Asia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004676-35 | Sponsor Protocol Number: RVT-1401-2001 | Start Date*: 2019-10-23 | |||||||||||
Sponsor Name:Immunovant Sciences GmbH | |||||||||||||
Full Title: ASCEND GO2: A Phase 2b, Multicenter, Randomized, Double-blind, Placebo-controlled Study of RVT-1401 for the Treatment of Patients with Active, Moderate to Severe Graves’ Ophthalmopathy | |||||||||||||
Medical condition: Graves´Ophthalmopathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003024-46 | Sponsor Protocol Number: Repha_1412 | Start Date*: 2014-09-19 | ||||||||||||||||
Sponsor Name:Repha GmbH | ||||||||||||||||||
Full Title: Efficacy, safety and tolerability of Angocin Anti-Infekt N versus Placebo for MRSA eradication | ||||||||||||||||||
Medical condition: MRSA colonisation | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-004734-17 | Sponsor Protocol Number: MV21118 | Start Date*: 2007-10-30 | |||||||||||
Sponsor Name:Terho Heikkinen | |||||||||||||
Full Title: A double-blind, randomized, placebo-controlled study of early oseltamivir treatment of influenza in children 1-3 years of age | |||||||||||||
Medical condition: Influenza | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002634-20 | Sponsor Protocol Number: NBF_HK_01_2018 | Start Date*: 2018-10-23 | ||||||||||||||||
Sponsor Name:Anaesthesia Department, Hvidovre Hospital, Capital Region of Denmark | ||||||||||||||||||
Full Title: Highdose steroid for total knee arthroplasty - A randomized doubleblindet controlled trial. | ||||||||||||||||||
Medical condition: Perioperative management of total knee-arthroplasty because of knee-osteoarthritis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-002636-25 | Sponsor Protocol Number: NBF_HK_03_2018 | Start Date*: 2018-10-23 | |||||||||||||||||||||
Sponsor Name:Anaesthesia Department, Hvidovre Hospital, Capital Region of Denmark. | |||||||||||||||||||||||
Full Title: Highdose Steroid for High Pain Responders undergoing Total Hip-arthroplasty - A randomized doubleblindet controlled trial. | |||||||||||||||||||||||
Medical condition: Perioperative management of total hip-arthroplasty because of hip-osteoarthritis | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: View results |
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