- Trials with a EudraCT protocol (44,380)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
44,380 result(s) found.
Displaying page 1,822 of 2,219.
| EudraCT Number: 2021-005575-40 | Sponsor Protocol Number: UZB-VHH2-4 | Start Date*: 2023-02-15 |
| Sponsor Name:UZ Brussel | ||
| Full Title: A phase II study to evaluate the imaging potential of 68GaNOTA-Anti-MMR VHH2 for in vivo imaging of MMR-expressing Macrophages by means of Positron Emission Tomography (PET) in patients with non-s... | ||
| Medical condition: Patients diagnosed with non-small cell lung cancer (NSCLC), planned for standard-of-care (SOC) surgery | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-002728-35 | Sponsor Protocol Number: HUN-AVI-01 | Start Date*: 2020-09-17 | |||||||||||
| Sponsor Name:Hungarian Ministry of Innovation and Technology - Representative: Hecrin Consortium | |||||||||||||
| 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: Patients with new type of coronavirus (SARS-CoV-2) infection proven by RT-PCR test with mild pneumonia. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-004928-42 | Sponsor Protocol Number: REM-ENY-01 | Start Date*: 2020-10-12 | |||||||||||
| Sponsor Name:Hungarian Ministry of Innovation and Technology - Representative: Hecrin Consortium | |||||||||||||
| Full Title: Open-label study to assess the safety of REMdesivir-HU as Eligible Novel therapY for moderate and severe Covid-19 patients | |||||||||||||
| Medical condition: SARS-CoV-2 Infection | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-005096-12 | Sponsor Protocol Number: OPRERA | Start Date*: 2021-05-31 | |||||||||||
| Sponsor Name:Karolinska Universitetssjukhuset | |||||||||||||
| Full Title: Utvärdering av två kortison behandlingsstrategier hos patienter med nydiagnostiserad, tidigare obehandlad reumatoid artrit: en randomiserad, öppen, non-inferiority klinisk studie | |||||||||||||
| Medical condition: Rheumatoid arthritis | |||||||||||||
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| Population Age: | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-003157-55 | Sponsor Protocol Number: EF-39 | Start Date*: 2023-03-30 | |||||||||||
| Sponsor Name:Novocure GmbH | |||||||||||||
| Full Title: PANOVA-4: Pilot, Single arm Study of Tumor Treating Fields (TTFields, 150kHz) Concomitant with Atezolizumab, Gemcitabine and Nab-Paclitaxel as First-Line Treatment for Metastatic Pancreatic Ductal ... | |||||||||||||
| Medical condition: Metastatic Pancreatic Ductal Adenocarcinoma (mPDAC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Prematurely Ended) CZ (Trial now transitioned) ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2023-000166-33 | Sponsor Protocol Number: SLICK-001 | Start Date*: 2023-04-12 | |||||||||||||||||||||||||||||||
| Sponsor Name:Semmelweis University | |||||||||||||||||||||||||||||||||
| Full Title: Implementation study of lipid management of high-risk cardiovascular patients- Semmelweis Lipid Center for high-risk patients | |||||||||||||||||||||||||||||||||
| Medical condition: primary hypercholesterolaemia (heterozygous familial and non-familial) or mixed dyslipidaemia in atherosclerotic cardiovascular disease | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: HU (Trial now transitioned) | |||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2020-005738-13 | Sponsor Protocol Number: TPLBIS20 | Start Date*: 2021-02-16 |
| Sponsor Name:Region Skåne | ||
| Full Title: Pivmecillinam with Amoxicillin/clavulanic acid for Step Down Oral Therapy in Febrile UTIs Caused by ESBL-producing Enterobacterales. | ||
| Medical condition: Urinary tract infection and/or bacteremia caused by extended spectrum beta-lactamases-producing Enterobacterales | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-003715-94 | Sponsor Protocol Number: IDEAL | Start Date*: 2020-12-17 |
| Sponsor Name:Institute for Clinical and Experimental Medicine | ||
| Full Title: INSULIN THERAPY DE-INTENSIFICATION WITH iGlarLixi | ||
| Medical condition: Type 2 diabetes mellitus | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: CZ (Completed) HU (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2022-000492-39 | Sponsor Protocol Number: XIN-XSTEM-201 | Start Date*: 2022-07-05 | |||||||||||
| Sponsor Name:Xintela AB | |||||||||||||
| Full Title: A multi-centre, randomised, single-blind Phase I/IIa study to evaluate the safety, tolerability and efficacy of a single topical dose of allogeneic integrin α10β1-selected mesenchymal stem cells (X... | |||||||||||||
| Medical condition: Difficult-to-heal venous leg ulcers | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-000810-72 | Sponsor Protocol Number: PREDIXLumB | Start Date*: 2014-12-05 | ||||||||||||||||||||||||||
| Sponsor Name:Karolinska University Hospital | ||||||||||||||||||||||||||||
| Full Title: PREDIX Luminal B - Neoadjuvant response-guided treatment of estrogen receptor positive tumors with high proliferation or slow proliferation with metastatic nodes or young patients. Part of a set of... | ||||||||||||||||||||||||||||
| Medical condition: Primary breast cancer | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: SE (Trial now transitioned) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2023-000945-18 | Sponsor Protocol Number: 219449 | Start Date*: 2024-10-28 | |||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||||||||||||||||||||||||||||||||
| Full Title: A Phase 2 single-blind, randomized, controlled, single center study to assess the immunogenicity and safety of a 2-dose schedule with GVGH altSonflex1-2-3 vaccine in African infants (H06_02TP) | |||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Prophylaxis for Shigellosis induced by Shigella sonnei, Shigella flexneri 1b, Shigella flexneri 2a and Shigella flexneri 3a. | |||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2020-001617-21 | Sponsor Protocol Number: 72864 | Start Date*: 2020-08-27 |
| Sponsor Name:Aarhus University Hospital | ||
| Full Title: The Effect of Trimetazidine on Mitochondrial Function, Myocardial Performance, and Invasive Hemodynamics in Patients Diagnosed with Wild-Type Transthyretin Cardiac Amyloidosis. | ||
| Medical condition: Wild-Type Transthyretin Cardiac Amyloidosis | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-003832-35 | Sponsor Protocol Number: HIPEC/FLOT9 | Start Date*: 2020-07-27 | |||||||||||
| Sponsor Name:Institute of Clinical Cancer Research (IKF) Krankenhaus Nordwest | |||||||||||||
| Full Title: Preventive HIPEC in combination with perioperative FLOT versus FLOT alone for resectable diffuse type gastric and gastroesophageal junction Type II/III adenocarcinoma – The phase III “PREVENT” tri... | |||||||||||||
| Medical condition: locally advanced resectable diffuse type adenocarcinoma of the oesophagogastric junction or the stomach | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-004981-37 | Sponsor Protocol Number: BMXBAR01 | Start Date*: 2022-01-19 |
| Sponsor Name:Helse Bergen HF | ||
| Full Title: Benzodiazepine maintenance treatment for patients with benzodiazepine dependence undergoing opioid agonist therapy (BMX-BAR) | ||
| Medical condition: Benzodiazepine dependence | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NO (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-000273-24 | Sponsor Protocol Number: RG_19-282 | Start Date*: 2020-10-06 | |||||||||||
| Sponsor Name:University of Birmingham | |||||||||||||
| Full Title: Venetoclax or Intensive Chemotherapy for Treatment Of Favourable Risk Acute Myeloid Leukaemia: A Molecularly Guided Phase 2 Study | |||||||||||||
| Medical condition: Acute Myeloid Leukaemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) DK (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-003009-31 | Sponsor Protocol Number: HH007 | Start Date*: 2022-12-23 | |||||||||||
| Sponsor Name:Zealand University Hospital, dept. of Haematology | |||||||||||||
| Full Title: Atorvastatin for patients with Philadelphia-negative chronic myeloproliferative neoplasms - Essential thrombocythemia, polycythemia vera and prefibrotic myelofibrosis | |||||||||||||
| Medical condition: Essential thrombocythemia, Polycythemia vera, prefibrotic myelofibrosis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-006497-23 | Sponsor Protocol Number: 870128 | Start Date*: 2022-07-05 |
| Sponsor Name:Helsinki University Hospital | ||
| Full Title: Corticosteroid in treatment of acute laryngitis among vocal professionals | ||
| Medical condition: Laryngitis | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: FI (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-005123-36 | Sponsor Protocol Number: PARASTOP | Start Date*: 2021-07-05 |
| Sponsor Name:Oslo University Hospital | ||
| Full Title: A randomized, double-blind, parallel-group non-inferiority phase III withdrawal trial of paracetamol versus placebo in conjunction with opioids for moderate to severe cancer-related pain | ||
| Medical condition: Adult patients with metastatic cancer disease, cancer-related pain treated with regular strong opioids, receiving paracetamol (1 gram three or four times a day) and with average pain intensity past... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NO (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-005376-29 | Sponsor Protocol Number: 2014-100757 | Start Date*: 2015-06-29 |
| Sponsor Name:Academic Medical Center, Gastroenterology | ||
| Full Title: An open-label observational phase 4 study to evaluate efficacy , safety and mucosal healing of early versus late use of vedolizumab in Crohn's disease: the LOVE-CD study (LOw countries VEdolizumab ... | ||
| Medical condition: Active Crohn's disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) BE (Completed) HU (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-000105-92 | Sponsor Protocol Number: CLMI070C12203 | Start Date*: 2021-10-15 | |||||||||||
| Sponsor Name:Novartis Pharma AG | |||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled Dose Range Finding Study with Open-Label Extension to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of LMI070/branaplam whe... | |||||||||||||
| Medical condition: Huntington's disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) HU (Completed) ES (Temporarily Halted) FR (Completed) IT (Prematurely Ended) BE (Completed) LT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
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