- Trials with a EudraCT protocol (43,861)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
43,861 result(s) found.
Displaying page 306 of 2,194.
EudraCT Number: 2019-004758-27 | Sponsor Protocol Number: IVIGPANSOpen | Start Date*: 2020-03-02 |
Sponsor Name:Gillberg Neuropsychiatry Centre | ||
Full Title: Intravenous immunoglobulin (IVIG) treatment in children with Pediatric Acute-onset Neuropsychiatric Syndrome (PANS): an open-label trial in South-western Sweden | ||
Medical condition: Pediatric Acute-onset Neuropsychiatric Syndrome (PANS) is a research diagnosis given to patients who have an abrupt, dramatic onset of neuropsychiatric symptoms including obsessions/compulsions and... | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-003492-29 | Sponsor Protocol Number: 391402 | Start Date*: 2016-03-02 | |||||||||||
Sponsor Name:Baxalta Innovations GmbH | |||||||||||||
Full Title: A Phase 1/2a, Open-Label, Parallel, Two-Arm, Dose-Escalation Study to Assess the Safety, Tolerability, Efficacy, Pharmacokinetics, and Pharmacodynamics of BAX69 in Subjects with Refractory Ovarian... | |||||||||||||
Medical condition: Refractory Ovarian Cancer with Malignant Ascites | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002129-12 | Sponsor Protocol Number: P150955 | Start Date*: 2016-10-12 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: A randomized phase IIb study of cyclophosphamide (Cy) versus anti-thymocyte globulin (ATG) for the prophylaxis of graft-versus-host disease (GVHD) after reduced-intensity conditioning allogeneic pe... | |||||||||||||
Medical condition: Women and men with a hematologic malignancy for which a reduced-intensity conditioning allo-SCT is indicated | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002164-41 | Sponsor Protocol Number: END-GH-2017 | Start Date*: 2017-07-03 | |||||||||||
Sponsor Name:Fundació Parc Taulí | |||||||||||||
Full Title: Growth hormone therapy in adults with Prader-Willi syndrome: Effect on muscle tone assessed by functional magnetic resonance imaging (fMRI) and its relation to muscle strenght and body composition. | |||||||||||||
Medical condition: Patients with Prader-Willi Syndrome (SPW) with Growth hormone deficit. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002741-29 | Sponsor Protocol Number: CMAA868A2202 | Start Date*: 2018-05-15 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A multicenter, randomized, open-label, active-controlled, dose-range finding study to assess the pharmacodynamic parameters, safety and tolerability of MAA868 and its effect on thrombogenesis bioma... | |||||||||||||
Medical condition: atrial fibrillation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Suspended by CA) SE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004524-29 | Sponsor Protocol Number: BECRO/PHN/LATIM | Start Date*: 2018-02-28 | |||||||||||||||||||||
Sponsor Name:PHARMATHEN | |||||||||||||||||||||||
Full Title: Therapeutic Equivalence (non-inferiority), Randomized, Observer-blind, two Parallel Group, Clinical Trial for Comparing the Efficacy and Tolerability of a new Generic Preservative-Free Formulation ... | |||||||||||||||||||||||
Medical condition: Open angle glaucoma or ocular hypertension. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GR (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-000450-21 | Sponsor Protocol Number: MONS4STRAT | Start Date*: 2018-04-09 |
Sponsor Name:Fundación Investigación Biomédica Hospital Ramón y Cajal | ||
Full Title: Prospective, Randomized, Open, Controlled, Multicenter Study to Evaluate the Safety and Efficacy of the MON4STRAT Approach for Optimizing Meropenem Therapy in Intubated and Mechanically-Ventilated,... | ||
Medical condition: Nosocomial pneumonia or severe tracheobronchitis caused by Gram-negative pathogens in subjects that requiring mechanical ventilation. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) FR (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000578-31 | Sponsor Protocol Number: Rostock-Benralizumab-2018-1 | Start Date*: 2018-07-05 |
Sponsor Name:University Medicine Rostock | ||
Full Title: Impact of benralizumab treatment on circulating dendritic cells in patients with eosinophilic asthma | ||
Medical condition: Eosinophilic Asthma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000615-25 | Sponsor Protocol Number: C-07-13 | Start Date*: 2018-04-05 | |||||||||||
Sponsor Name:Alcon Research Ltd | |||||||||||||
Full Title: Safety and Efficacy Evaluation of Topical Moxidex Otic Solution in the Treatment of Acute Otitis Externa | |||||||||||||
Medical condition: Acute Otitis Externa | |||||||||||||
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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: 2017-004715-40 | Sponsor Protocol Number: BRU-VCN-2017 | Start Date*: 2018-07-04 |
Sponsor Name:Fundació Hospital Universitari Vall d’Hebron-Institut de Recerca (VHIR) | ||
Full Title: An effectiveness and safety study of Varenicline for smoking cessation in hospitalized patients with psychiatric disorders. | ||
Medical condition: Smoking cessation in hospitalized patients with psychiatric disorders. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2019-003836-22 | Sponsor Protocol Number: FLG-V001 | Start Date*: 2019-12-11 | |||||||||||
Sponsor Name:HUS Helsinki University Hospital | |||||||||||||
Full Title: TWO-STAGE, TWO-ARM, OPEN-LABEL PHASE II STUDY OF VENETOCLAX IN COMBINATION WITH AZACYTIDINE IN ACUTE MYELOID LEUKEMIA PATIENTS SELECTED USING EX VIVO DRUG SENSITIVITY SCREENING | |||||||||||||
Medical condition: Acute myeloid leukemia in patients who are non-fit for standard induction therapy (except acute promyelocytic leukemia) and present with de novo, secondary, released or refractory AML | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004766-15 | Sponsor Protocol Number: MK-0518B-254 | Start Date*: 2015-05-04 |
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | ||
Full Title: MK-518B Food Effect Study | ||
Medical condition: N/A | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2014-005127-27 | Sponsor Protocol Number: CIGE025ENL01T | Start Date*: 2015-05-29 |
Sponsor Name:UMC Utrecht | ||
Full Title: Markers of Efficacy of Xolair (Omalizumab) in Chronic Spontaneous Urticaria | ||
Medical condition: Chronic spontaneous urticaria | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-003370-33 | Sponsor Protocol Number: M15-684 | Start Date*: 2016-01-05 |
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | ||
Full Title: An Open-Label, Single Arm Study to Evaluate the Safety and Efficacy of Ombitasvir/Paritaprevir/Ritonavir and Dasabuvir in Treatment-Naïve Adults With Genotype 1b Hepatitis C Virus (HCV) Without Cir... | ||
Medical condition: Hepatitis C Infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) GB (Completed) ES (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-002106-36 | Sponsor Protocol Number: JNJ-DEP | Start Date*: 2016-01-11 | ||||||||||||||||
Sponsor Name:Clinirx Tangent Research | ||||||||||||||||||
Full Title: The effects of JNJ-39393406 on psychometric performance and residual depressive symptoms in 80 patients with unipolar or bipolar depression: a phase II exploratory add-on double blind placebo contr... | ||||||||||||||||||
Medical condition: Unipolar and bipolar depression | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: RO (Suspended by CA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002811-13 | Sponsor Protocol Number: PARTNER | Start Date*: 2016-01-25 | |||||||||||
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust and the University of Cambridge | |||||||||||||
Full Title: Randomised, phase II/III, 3 stage trial to evaluate the safety and efficacy of the addition of olaparib to platinum-based neoadjuvant chemotherapy in breast cancer patients with TNBC and/or gBRCA | |||||||||||||
Medical condition: ER negative and HER2 negative Early Breast Cancer or BRCA 1 or 2 germline mutated Early Breast Cancer | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002494-34 | Sponsor Protocol Number: H9X-MC-GBGJ | Start Date*: 2016-12-06 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Phase 2, Double-Blind, Placebo-Controlled, 18-Week Trial of Investigational Dulaglutide Doses versus Placebo in Patients with Type 2 Diabetes on Metformin Monotherapy | |||||||||||||
Medical condition: Type 2 Diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003641-14 | Sponsor Protocol Number: D5136C00010 | Start Date*: 2018-01-29 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Multi-centre, Phase I, Open-label, Single-dose Study to Investigate Pharmacokinetics (PK) of Ticagrelor in Infants and Toddlers, Aged 0 to less than 24 Months, with Sickle Cell Disease | |||||||||||||
Medical condition: Sickle Cell Disease | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) ES (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003638-10 | Sponsor Protocol Number: 2016_37 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:CHRU LILLE | |||||||||||||
Full Title: INTRANASAL CLONIDINE PREDICTION IN PEDIATRIC SURGERY: RANDOMIZED STUDY AGAINST PLACEBO | |||||||||||||
Medical condition: intra-nasal premedication instead of oral, intravenous or no premedication. | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001502-28 | Sponsor Protocol Number: PRED-AID | Start Date*: 2019-02-11 | |||||||||||
Sponsor Name:Imperial College London | |||||||||||||
Full Title: Safety and Efficacy of Prednisolone in Adrenal Insufficiency Disease (PRED-AID Study) | |||||||||||||
Medical condition: Adrenal insufficiency | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
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