- Trials with a EudraCT protocol (44,394)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
44,394 result(s) found.
Displaying page 2,034 of 2,220.
| EudraCT Number: 2016-003722-16 | Sponsor Protocol Number: 205419 | Start Date*: 2020-05-12 | |||||||||||
| Sponsor Name:GlaxoSmithKline Biologicals S.A. | |||||||||||||
| Full Title: A Phase IIIB, randomized, observer-blind, multicenter study to assess the safety and immunogenicity of GSK’s meningococcal group B vaccine when administered concomitantly with GSK’s meningococcal M... | |||||||||||||
| Medical condition: Healthy volunteers (Active immunization against invasive meningococcal disease caused by 5 different serogroups of N. meningitidis by concomitant administration of meningococcal group B vaccine a... | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-003835-12 | Sponsor Protocol Number: AC17067 | Start Date*: 2018-03-01 | |||||||||||||||||||||
| Sponsor Name:The University Of Edinburgh [...] | |||||||||||||||||||||||
| Full Title: A placebo controlled randomised trial of intravenous lidocaine in accelerating gastrointestinal recovery after colorectal surgery | |||||||||||||||||||||||
| Medical condition: Patients scheduled for elective colorectal resection for colorectal cancer or diverticular disease. | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2022-001097-64 | Sponsor Protocol Number: CVD19-ESCIN | Start Date*: 2022-07-14 | |||||||||||
| Sponsor Name:UAB Švenčionių vaistažolės | |||||||||||||
| Full Title: An open-label, randomized, parallel-controlled, phase II clinical trial to evaluate the tolerability, efficacy and safety of Aesculus Hippocastanum L seed extract in COVID-19 patients with mild pne... | |||||||||||||
| Medical condition: COVID-19 patients with mild pneumonia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: LT (Prohibited by CA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-005128-12 | Sponsor Protocol Number: T705-COVID-GCRI-Protocol-A | Start Date*: 2021-02-01 |
| Sponsor Name:Vilnius University Hospital Santaros klinikos | ||
| Full Title: An Investigation of the Efficacy and Safety of Favipiravir in COVID-19 Patients with Mild Pneumonia − An open-label randomized controlled study | ||
| Medical condition: COVID-19 Patients with Mild Pneumonia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: LT (Prohibited by CA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-005214-18 | Sponsor Protocol Number: T705-COVID-GCRI-Protocol-B | Start Date*: 2021-02-01 |
| Sponsor Name:Vilnius University Hospital Santaros klinikos | ||
| Full Title: An Investigation of the Efficacy and Safety of Favipiravir in COVID-19 Patients without Pneumonia − An open-label randomized controlled study | ||
| Medical condition: COVID-19 Patients without Pneumonia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: LT (Prohibited by CA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-000036-96 | Sponsor Protocol Number: CR0014 | Start Date*: 2018-09-06 | |||||||||||
| Sponsor Name:Ablative Solutions, Inc. | |||||||||||||
| Full Title: A Phase 2, Multicenter, Blinded, Sham Procedure-Controlled Trial of Renal Denervation by the Peregrine System Kit, in Subjects with Hypertension, in the Absence of Antihypertensive Medications | |||||||||||||
| Medical condition: Hypertension | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) GB (GB - no longer in EU/EEA) DE (Completed) IE (Completed) NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-002588-17 | Sponsor Protocol Number: SAM-IIT01 | Start Date*: 2019-10-21 |
| Sponsor Name:Universitätsklinikum Tübingen | ||
| Full Title: Safety and effects on visual function of 0.01% Atropin eye drops for myopia inhibition in children and adolescents | ||
| Medical condition: Myopia | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-004607-24 | Sponsor Protocol Number: FICBMRISTUDY2016 | Start Date*: 2016-08-09 |
| Sponsor Name:AZ Groeninge | ||
| Full Title: Comparison of the spread of local anesthetics in the fascia iliaca compartment between the classical “transverse” technique and the longitudinal supra-inguinal technique. | ||
| Medical condition: The aim of the study is to compare the spread of local anaesthetics between the classical FICB (cFICB) and the supra-inguinal FICB (sFICB). The spread of local anesthetic in the fascia iliaca compa... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2023-000102-25 | Sponsor Protocol Number: PRECISION | Start Date*: 2023-05-30 | |||||||||||
| Sponsor Name:Hellenic Institute for the Study of Sepsis | |||||||||||||
| Full Title: SAFETY AND EFFICACY OF ANAKINRA TREATMENT FOR PATIENTS WITH PERSISENT RESPIRATORY SYMPTOMS POST ACUTE COVID AND IMMUNE SYSTEM ACTIVATION: THE PRECISION DOUBLE-BLIND, RANDOMIZED CLINICAL TRIAL | |||||||||||||
| Medical condition: Post-acute COVID-19 syndrome (PACS) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-002767-30 | Sponsor Protocol Number: ACT17453 | Start Date*: 2023-02-23 | |||||||||||
| Sponsor Name:Sanofi-aventis recherche & developpement | |||||||||||||
| Full Title: A randomized, Phase 2, open label study evaluating subcutaneous administration of isatuximab in combination with carfilzomib and dexamethasone in adult participants with relapsed and/or refractory ... | |||||||||||||
| Medical condition: Relapsed/refractory multiple myeloma (RRMM) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Trial now transitioned) GR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-002265-15 | Sponsor Protocol Number: BO44157 | Start Date*: 2023-03-27 | |||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
| Full Title: A PHASE II, RANDOMIZED, MULTICENTER, OPEN LABEL, CONTROLLED STUDY OF RO7247669 ALONE OR IN COMBINATION WITH TIRAGOLUMAB VERSUS ATEZOLIZUMAB IN PATIENTS WITH PREVIOUSLY UNTREATED LOCALLY ADVANCED OR... | |||||||||||||
| Medical condition: Previously Untreated Locally Advanced or Metastatic Urothelial Bladder Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) GR (Trial now transitioned) DK (Trial now transitioned) IT (Trial now transitioned) DE (Trial now transitioned) ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-022064-12 | Sponsor Protocol Number: EFC11784 | Start Date*: 2011-03-23 | |||||||||||
| Sponsor Name:sanofi-aventis R&D | |||||||||||||
| Full Title: Randomized, Open Label, Multi-Center Study comparing Cabazitaxel at 25 mg/m2 and at 20 mg/m² in Combination with Prednisone Every 3 Weeks to Docetaxel in Combination with Prednisone in Patients wit... | |||||||||||||
| Medical condition: metastatic Castration Resistant Prostate cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: SE (Completed) CZ (Completed) ES (Completed) FI (Completed) DK (Completed) PT (Completed) IT (Completed) DE (Completed) RO (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-000836-49 | Sponsor Protocol Number: MK-3475-D46 | Start Date*: 2023-01-16 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme LLC | |||||||||||||
| Full Title: An Open-label, Multicenter, Phase 3 Randomized, Active-Comparator-Controlled Clinical Study of Pembrolizumab (MK-3475) in Combination With Sacituzumab Govitecan Versus MK-3475 Monotherapy as First-... | |||||||||||||
| Medical condition: First-line treatment of metastatic programmed cell death ligand 1 expressing (tumor proportion score ≥50%) non-small cell lung cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Trial now transitioned) GR (Trial now transitioned) LT (Trial now transitioned) IT (Trial now transitioned) LV (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-006781-21 | Sponsor Protocol Number: COAV101A12308 | Start Date*: 2022-10-31 | |||||||||||
| Sponsor Name:Novartis Pharma AG | |||||||||||||
| Full Title: Long-term follow-up of patients with spinal muscular atrophy Treated with OAV101 IT or OAV101 IV in Clinical Trials | |||||||||||||
| Medical condition: Spinal Muscular Atrophy | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Trial now transitioned) FR (Trial now transitioned) IT (Trial now transitioned) DE (Completed) DK (Trial now transitioned) ES (Ongoing) GR (Prematurely Ended) NL (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-003114-13 | Sponsor Protocol Number: PACEACE | Start Date*: 2020-01-31 |
| Sponsor Name:Med. Univ. Wien, Klinik f. Innere Med. I, Onkologie | ||
| Full Title: Paclitaxel plus cetuximab for the treatment of recurrent and/or metastatic head and neck cancer after first-line checkpoint inhibitor failure: A multicenter, single arm study | ||
| Medical condition: Recurrent and/or metastatic head and neck cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) DE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-003179-32 | Sponsor Protocol Number: ToL54304 | Start Date*: 2016-02-03 | |||||||||||||||||||||
| Sponsor Name:University Medical Center Utrecht | |||||||||||||||||||||||
| Full Title: PREvention of Complications to Improve Outcome in elderly patients with acute Stroke. A randomised, open, phase III, clinical trial with blinded outcome assessment. | |||||||||||||||||||||||
| Medical condition: Stroke (ischaemic stroke or intracerebral hemorrhage) | |||||||||||||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: NL (Completed) HU (Completed) GR (Completed) IT (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2008-003803-30 | Sponsor Protocol Number: 2560/2008 | Start Date*: 2011-04-28 | ||||||||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA PISANA | ||||||||||||||||||
| Full Title: Effects of the treatment with metformin and/or sitagliptin on β- cell function and insulin resistance in women with prior gestational diabetes. | ||||||||||||||||||
| Medical condition: previous gestational diabetes | ||||||||||||||||||
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| Population Age: Adults | Gender: Female | |||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2018-000487-28 | Sponsor Protocol Number: PROTECTION | Start Date*: 2018-08-06 | |||||||||||
| Sponsor Name:OSPEDALE SAN RAFFAELE | |||||||||||||
| Full Title: Intravenous amino acid therapy for kidney protection in cardiac surgery: a multi-centre randomised blinded placebo controlled clinical trial | |||||||||||||
| Medical condition: Patients undergoing cardiac surgery at risk for developing acute kidney injury | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-002523-26 | Sponsor Protocol Number: WI88341 | Start Date*: 2016-03-08 | |||||||||||
| Sponsor Name:Arthritis Alapítvány | |||||||||||||
| Full Title: Effects of JAK inhibition on rheumatoid arthritis-related comorbidities: link between bone and vascular effects (investigator-initiated grant proposal) | |||||||||||||
| Medical condition: Rheumatoid Arthritis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-000977-35 | Sponsor Protocol Number: AtezoTRIBE | Start Date*: 2018-09-13 | |||||||||||
| Sponsor Name:G.O.N.O. - GRUPPO ONCOLOGICO DEL NORD OVEST | |||||||||||||
| Full Title: Randomized phase II study of FOLFOXIRI plus BEVACIZUMAB plus ATEZOLIZUMAB versus FOLFOXIRI plus BEVACIZUMAB as first-line treatment of unresectable metastatic colorectal cancer patients | |||||||||||||
| Medical condition: Metastatic Colorectal Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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