- Trials with a EudraCT protocol (44,341)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,341 result(s) found.
Displaying page 1,549 of 2,218.
EudraCT Number: 2004-001688-23 | Sponsor Protocol Number: NA17598C | Start Date*: 2004-10-27 |
Sponsor Name:F. Hoffmann-La Roche Ltd | ||
Full Title: A multicentre, double-blind, placebo-controlled randomized trial of the efficacy, safety and tolerability of 12 months of once daily treatment with 1 mg of RO3300074 in patients with symptomatic em... | ||
Medical condition: symptomatic emphysema secondary to alpha-1-antitrypsin deficiency | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) GB (Completed) DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-004181-37 | Sponsor Protocol Number: B9371039 | Start Date*: 2023-02-03 |
Sponsor Name:Pfizer Inc. | ||
Full Title: A PHASE 3, SINGLE-ARM, OPEN-LABEL STUDY TO EVALUATE THE IMMUNOGENICITY, SAFETY, AND TOLERABILITY OF A TICK-BORNE ENCEPHALITIS VACCINE IN HEALTHY JAPANESE PARTICIPANTS 1 YEAR OF AGE AND OLDER | ||
Medical condition: Active immunization to prevent tick borne encephalitis (TBE) | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2008-008258-21 | Sponsor Protocol Number: NV20536 eu | Start Date*: 2009-03-30 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A Randomized, Double-blinded, Multicenter, Dose and Duration Finding Study to Evaluate the Sustained Virologic Response of the HCV Polymerase Inhibitor Prodrug (RO5024048) in Combination with Pegas... | |||||||||||||
Medical condition: Chronic Hepatitis C | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) DE (Completed) ES (Completed) FR (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001337-40 | Sponsor Protocol Number: BXCL501-105 | Start Date*: 2021-10-05 | |||||||||||||||||||||
Sponsor Name:BioXcel Therapeutics, Inc. | |||||||||||||||||||||||
Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO DETERMINE EFFICACY AND SAFETY OF BXCL501 IN AGITATION ASSOCIATED WITH PEDIATRIC SCHIZOPHRENIA AND BIPOLAR DISORDER | |||||||||||||||||||||||
Medical condition: Subject that meets DSM-5 criteria for schizophrenia, schizoaffective, or schizophreniform disorder, or other specified/unspecified schizophrenia spectrum and/or other psychotic disorders OR Subjec... | |||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Restarted) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004612-23 | Sponsor Protocol Number: TV-3326/201 | Start Date*: 2005-04-13 | |||||||||||
Sponsor Name:Teva Pharmaceutical Industries Ltd | |||||||||||||
Full Title: A multi-center, randomized, double-blind, placebo-controlled, sequential cohort designed, escalating dose study to assess the tolerability, safety and maximal tolerated dose (MTD) of Ladostigil in ... | |||||||||||||
Medical condition: Patients with probable Alzheimer's Disease (AD) diagnosis according to NINCDS-ADRDA and DSM–IV criteria, who suffer from mild to moderate dementia with a Mini Mental State Examination (MMSE) of 15-26 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-004073-31 | Sponsor Protocol Number: 2021/1001 | Start Date*: 2022-01-17 | |||||||||||
Sponsor Name:University Medical Center Groningen | |||||||||||||
Full Title: Treating microalbuminuria over 24 weeks in subjects with or without type 2 diabetes or hypertension | |||||||||||||
Medical condition: Microalbuminuria | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004478-24 | Sponsor Protocol Number: OV101-18-002 | Start Date*: 2020-06-05 | |||||||||||
Sponsor Name:Ovid Therapeutics Inc. | |||||||||||||
Full Title: An Open-Label Study to Evaluate the Long-Term Safety, Tolerability, and Efficacy of OV101 in Individuals with Angelman Syndrome (ELARA) | |||||||||||||
Medical condition: Angelman Syndrome | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000249-38 | Sponsor Protocol Number: R118439 | Start Date*: 2019-01-25 | |||||||||||
Sponsor Name:University of Manchester | |||||||||||||
Full Title: Phase II trial of interleukin-1 receptor antagonist in intracerebral haemorrhage: BLOcking the Cytokine IL-1 in ICH | |||||||||||||
Medical condition: intracerebral haemorrhage | |||||||||||||
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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: 2016-003709-33 | Sponsor Protocol Number: AIO-HEP-0116 | Start Date*: 2017-05-04 | |||||||||||||||||||||||||||||||
Sponsor Name:AIO-Studien-gGmbH | |||||||||||||||||||||||||||||||||
Full Title: A randomized phase II trial of nal-IRI and 5-Fluorouracil compared to 5-Fluorouracil in patients with cholangio- and gallbladder carcinoma previously treated with gemcitabine-based therapies | |||||||||||||||||||||||||||||||||
Medical condition: advanced, unresectable and metastatic cholangio- and gallbladder carcinoma | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001632-19 | Sponsor Protocol Number: MVT-601-3102 | Start Date*: 2017-12-01 | |||||||||||
Sponsor Name:Myovant Sciences GmbH | |||||||||||||
Full Title: SPIRIT 2: An International Phase 3 Randomized, Double-Blind, Placebo-Controlled Efficacy and Safety Study to Evaluate Relugolix Administered with and without Low-Dose Estradiol and Norethindrone Ac... | |||||||||||||
Medical condition: Endometriosis | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: SE (Completed) CZ (Completed) PL (Completed) GB (Completed) IT (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000615-24 | Sponsor Protocol Number: 20121903114 | Start Date*: 2014-03-11 |
Sponsor Name:Cliniques universitaires Saint-Luc | ||
Full Title: Tacrolimus disposition in pediatric transplantation: influence of age, genetic polymorphisms, intestinal and hepatic relative contribution on pharmacokinetics, in relationship with clinical outco... | ||
Medical condition: PEDIATRIC LIVER TRANSPLANTATION | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: BE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2011-001139-22 | Sponsor Protocol Number: POPH | Start Date*: 2011-06-29 | |||||||||||
Sponsor Name:Medizinische Universität Graz, Klin. Abteilung für Gastroenterologie und Hepatologie | |||||||||||||
Full Title: AMBRISENTAN FOR TREATMENT OF PORTOPULMONARY HYPERTENSION (POPH): A PILOT STUDY | |||||||||||||
Medical condition: Portopulmonary Hypertension (PoPH) and Hepatopulmonary Syndrome HPS are present in a considerable number of patients with compensated cirrhosis. Treatment of PoPH with ambrisentan is well tolerated... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016829-34 | Sponsor Protocol Number: 06644329988 | Start Date*: 2010-07-28 |
Sponsor Name:Medizinische Universität Graz, Klinische Abteilung für Thorax -u. Hyperbare Chirurgie | ||
Full Title: Influence of perioperative administration of diclovenac-natrium/orfendadrincitrate on the recurrence rate of surgically treated spontaneous pneumothorax | ||
Medical condition: Spontaneous pneumothorax | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-002678-10 | Sponsor Protocol Number: GF22002 | Start Date*: 2023-03-07 |
Sponsor Name:Ginefiv | ||
Full Title: Protocol with progestin-primed ovarian stimulation (PPOS) starting on day 5 versus protocol with progestin-primed ovarian stimulation (PPOS) in a conventional regimen from the start of the ovaria... | ||
Medical condition: Number of MII oocytes obtained in both groups | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2022-003913-12 | Sponsor Protocol Number: 22/589-EC_M. | Start Date*: 2023-03-07 |
Sponsor Name:COMPLUTENSE UNIVERSITY OF MADRID | ||
Full Title: Diode laser and photodynamic therapy Versus Ciclopirox Hydroxypropyl Chitosan. Randomised controlled clinical trial. | ||
Medical condition: Onychomycosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2022-003861-39 | Sponsor Protocol Number: GLUCOTAVI | Start Date*: 2023-03-07 |
Sponsor Name:JUAN MIGUEL RUIZ NODAR | ||
Full Title: Glucocorticoid treatment in patients undergoing TAVI to reduce the incidence of atrioventricular block and pacemaker implantation | ||
Medical condition: aortic stenosis | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-004749-40 | Sponsor Protocol Number: PEDMet 2006-1 | Start Date*: 2006-11-20 |
Sponsor Name:Pediatrics | ||
Full Title: Glucose metabolism in patients with neurological/neuromuscular diseases. | ||
Medical condition: Patients with neurological/neuromuscular diseases | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-002912-73 | Sponsor Protocol Number: AL-JVC-05-01 | Start Date*: 2005-08-02 |
Sponsor Name:University Hospitals Leuven | ||
Full Title: An Open Label Evaluation of Efficacy and Safety of Posterior Juxtascleral Administrations of 15 mg Anecortave Acetate for Depot Suspension Combined with Verteporfin Therapy in Patients with Exudati... | ||
Medical condition: Age Related Macular Degeneration with Retino-choroidal Anastomosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2022-002801-36 | Sponsor Protocol Number: Can-201 | Start Date*: 2023-03-08 | |||||||||||
Sponsor Name:Cantex Pharmaceuticals Inc. | |||||||||||||
Full Title: A Phase I/II Open Label Study to Assess Safety and Preliminary Evidence of a Therapeutic Effect of Azeliragon Combined with Conventional Concurrent Radiation and Temozolomide in Patients with Newly... | |||||||||||||
Medical condition: Newly diagnosed glioblastoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001939-38 | Sponsor Protocol Number: NIVINIHO | Start Date*: 2018-04-18 | |||||||||||
Sponsor Name:LYSARC | |||||||||||||
Full Title: A prospective phase II study of nivolumab alone, or in combination with vinblastin in patients aged 61 years and older, with classical Hodgkin Lymphoma and coexisting medical conditions | |||||||||||||
Medical condition: patients aged 61 years and older, with classical Hodgkin lymphoma and coexisting medical conditions | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
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