- Trials with a EudraCT protocol (11,654)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
11,654 result(s) found for: 30 - 15.
Displaying page 89 of 583.
| EudraCT Number: 2017-002774-39 | Sponsor Protocol Number: PDY15079 | Start Date*: 2018-01-23 | |||||||||||
| Sponsor Name:SANOFI-AVENTIS RECHERCHE ET DEVELOPPEMENT | |||||||||||||
| Full Title: An Exploratory, Randomized, Double-blind, Placebo-controlled, Parallel Arm Trial of the Safety and Pharmacodynamic Activity of Sotagliflozin in Hemodynamically Stable Patients with Worsening Heart ... | |||||||||||||
| Medical condition: Cardiac Failure aggravated | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-001327-23 | Sponsor Protocol Number: ITP0815 | Start Date*: 2015-06-26 | |||||||||||
| Sponsor Name:Fondazione G.I.M.EM.A. Gruppo Italiano Malattie Ematologiche dell'Adulto | |||||||||||||
| Full Title: Eltrombopag as Second line Therapy in adult patients with primary Immune Thrombocytopenia (ESTIT study) in an attempt to achieve long-term remission: a single arm multicenter phase II clinical and ... | |||||||||||||
| Medical condition: Primary Immune Thrombocytopenia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-000844-56 | Sponsor Protocol Number: TOPAS2011 | Start Date*: 2011-07-12 | |||||||||||
| Sponsor Name:Charité Universitätsmedizin Berlin | |||||||||||||
| Full Title: UsTekinumab for the treatment Of Patients with active Ankylosing Spondylitis (TOPAS) – a 28-week, prospective, open-label, proof-of-concept study | |||||||||||||
| Medical condition: Ankylosing spondylitis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-003406-14 | Sponsor Protocol Number: UHNM1219 | Start Date*: 2017-09-26 | |||||||||||||||||||||
| Sponsor Name:University Hospital of North Midlands NHS Trust | |||||||||||||||||||||||
| Full Title: The Metoclopramoide and selective oral decontamination for Avoiding Pneumonia after Stroke (MAPS-2) Trial: a 2x2 double-blind, randomized controlled trial of metoclopramide and selective oral decon... | |||||||||||||||||||||||
| Medical condition: Stroke We are testing two differnt intervetnions which could prevent pneumonia in stroke patietns. Prevention pneumonia could potentiallly speed up recovery and improve survival. | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2013-002409-75 | Sponsor Protocol Number: Dota-PrimoLIV | Start Date*: 2014-01-06 | ||||||||||||||||
| Sponsor Name:Charite | ||||||||||||||||||
| Full Title: Intra-individual, comparison of the MRI contrast agents gadoxetic acid (Primovist®) versus gadoterate meglumine (Dotarem®) in liver MRI of patients with HCC and underlying cirrhosis | ||||||||||||||||||
| Medical condition: Patients with liver cirrhosis and diagnosis of hepatocellular carcinoma based on noninvasive HCC diagnostic (EASL) criteria | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2017-004459-21 | Sponsor Protocol Number: Co-ALS | Start Date*: 2018-09-11 | ||||||||||||||||
| Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA POLICLINICO DI MODENA | ||||||||||||||||||
| Full Title: Colchicine for Amyotrophic Lateral Sclerosis: a phase II, randomized, double blind, placebo controlled, multicenter clinical trial | ||||||||||||||||||
| Medical condition: Definite or probable amyotrophic lateral sclerosis | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2012-002291-13 | Sponsor Protocol Number: DIALAGG | Start Date*: 2012-10-19 | |||||||||||
| Sponsor Name:InfectoPharm - Arzneimittel und Consilium GmbH | |||||||||||||
| Full Title: Multicentre, prospective, double-blind, two-armed, placebo-controlled phase III study to evaluate the efficacy and safety of the treatment of diarrhoea with Lactobacillus rhamnosus GG (InfectoDiarr... | |||||||||||||
| Medical condition: Acute diarrhoea in infants and toddlers | |||||||||||||
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| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-003014-12 | Sponsor Protocol Number: COPERNICOS_JUJCPR | Start Date*: 2021-03-19 | |||||||||||
| Sponsor Name:Chronic Obstructive Pulmonary Disease Trial Network (COP:TRIN) | |||||||||||||
| Full Title: COPD - Eosinophil-guided Reduction of Inhaled COrticoSteroids (COPERnICOS) | |||||||||||||
| Medical condition: Clinicaltrial on eosinophil-guided time-updated person-specific reduction of inhaled corticosteroid therapy and prophylactic azithromycin therapy in patients with severe or very severe chronic obst... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-000492-32 | Sponsor Protocol Number: AMIII | Start Date*: 2019-01-14 |
| Sponsor Name:Charité-Universitätsmedizin Berlin | ||
| Full Title: Effects of antibiotics on micobiota, pulmonary immune response and incidence of ventilator-associated infections | ||
| Medical condition: mechanically ventilated patients | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2022-003561-38 | Sponsor Protocol Number: APHP220729 | Start Date*: 2023-08-23 | |||||||||||
| Sponsor Name:Assistance publique - Hôpitaux de Paris | |||||||||||||
| Full Title: Durvalumab/Tremelimumab in neoadjuvant and adjuvant setting in patients with HCC treated by electroporation ablation in curative intent: French multicenter phase 2 therapeutic DUMELEP trial (DUMELEP) | |||||||||||||
| Medical condition: Hepatocellular carcinoma (HCC) | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-000637-13 | Sponsor Protocol Number: CRAP-ACStrial | Start Date*: 2022-02-08 | ||||||||||||||||||||||||||
| Sponsor Name:AZIENDA USL TOSCANA CENTRO | ||||||||||||||||||||||||||||
| Full Title: Cardiac and renal protective effect of colchicine early on-admission administered in patient with acute coronaric syndrome in treatment with atorvastatin | ||||||||||||||||||||||||||||
| Medical condition: sindrome coronarica acuta (ACS) statin-naive con indicazione ad una strategia invasiva di rivascolarizzazione che vengono ricoverati in reparto cardiologico. | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2018-001404-11 | Sponsor Protocol Number: TEM-GBM_001 | Start Date*: 2018-09-26 | ||||||||||||||||||||||||||
| Sponsor Name:GENENTA SCIENCE SRL | ||||||||||||||||||||||||||||
| Full Title: A phase I/IIa dose escalation study evaluating the safety and efficacy of autologous CD34+-enriched hematopoietic progenitor cells genetically modified with a lentiviral vector encoding for the hum... | ||||||||||||||||||||||||||||
| Medical condition: Glioblastoma Multiforme | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: IT (Trial now transitioned) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2021-000311-23 | Sponsor Protocol Number: PS-CLL-008 | Start Date*: 2021-06-04 | |||||||||||
| Sponsor Name:OSPEDALE SAN RAFFAELE | |||||||||||||
| Full Title: Fixed-duration therapy with ibrutinib and obinutuzumab (GA-101) in treatment-naïve patients with CLL | |||||||||||||
| Medical condition: chronic lymphocytic leukemia/small lymphocytic lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-001963-25 | Sponsor Protocol Number: SNOXA12C701 | Start Date*: 2022-04-07 | |||||||||||
| Sponsor Name:NOXXON Pharma AG | |||||||||||||
| Full Title: An Open-label Phase 2 Study of Olaptesed Pegol (NOX-A12) Combined with Pembrolizumab and Nanoliposomal Irinotecan/5-FU/Leucovorin or Gemcitabine/nab-Paclitaxel inMicrosatellite-Stable Metastatic Pa... | |||||||||||||
| Medical condition: Pancreatic cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-004490-10 | Sponsor Protocol Number: 2012_32 | Start Date*: 2013-09-18 | |||||||||||
| Sponsor Name:Ghent University Hospital | |||||||||||||
| Full Title: A Multicenter Open label Phase 2 study of Carfilzomib Weekly plus Melphalan and Prednisone in Untreated Symptomatic Elderly Multiple Myeloma. | |||||||||||||
| Medical condition: A Multicenter Open label Phase 2 study of Carfilzomib Weekly plus Melphalan and Prednisone in Untreated Symptomatic Elderly Multiple Myeloma. | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-000874-92 | Sponsor Protocol Number: LUM-201-01 | Start Date*: 2021-03-22 | |||||||||||
| Sponsor Name:Lumos Pharma, Inc. | |||||||||||||
| Full Title: A Multicenter, 24-Month, Randomized, Open-Label, Active Control, Parallel Arm, Phase 2 Study of Daily Oral LUM-201 in Naïve-to-Treatment, Prepubertal Children with Idiopathic Growth Hormone Deficie... | |||||||||||||
| Medical condition: Growth hormone deficiency | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-005318-11 | Sponsor Protocol Number: 0602308 | Start Date*: 2007-07-06 | |||||||||||
| Sponsor Name:CHU Toulouse | |||||||||||||
| Full Title: Effet de l'apomorphine sur la perception douloureuse chez le patient parkinsonien : étude clinique et en tomographie par émission de positons. | |||||||||||||
| Medical condition: maladie de Parkinson | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-005339-22 | Sponsor Protocol Number: REGBONE | Start Date*: Information not available in EudraCT | ||||||||||||||||||||||||||
| Sponsor Name:Instytut Matki i Dziecka | ||||||||||||||||||||||||||||
| Full Title: To evaluate the efficacy and safety of regorafenib in patients with refractory primary bone tumors. | ||||||||||||||||||||||||||||
| Medical condition: Refractory primary bone tumors | ||||||||||||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: PL (Trial now transitioned) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2008-005667-34 | Sponsor Protocol Number: G0701625 | Start Date*: 2009-01-16 | |||||||||||
| Sponsor Name:University of Edinburgh [...] | |||||||||||||
| Full Title: Randomised Trial of Genetic Testing and Targeted Zoledronic acid therapy to Prevent SQSTM1 Mediated Paget's Disease (Zoledronate in the Prevention of Paget's). | |||||||||||||
| Medical condition: Paget's disease of the bone (PDB) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) IT (Completed) IE (Completed) ES (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2024-000481-17 | Sponsor Protocol Number: EBSI-CV-317-008 | Start Date*: 2025-08-28 | |||||||||||
| Sponsor Name:Bavarian Nordic A/S | |||||||||||||
| Full Title: A Long-term Follow-up Study to Evaluate Safety and Immunogenicity of a Chikungunya Virus Virus-like Particle Vaccine (PXVX0317) in Healthy Adults and Adolescents After Either a Single or a Booster ... | |||||||||||||
| Medical condition: Healthy Volunteers (Chikungunya disease. The study evaluates safety and immunogenicity) | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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