- Trials with a EudraCT protocol (16)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
16 result(s) found for: Mass communication.
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EudraCT Number: 2019-003524-20 | Sponsor Protocol Number: BP41316 | Start Date*: 2020-12-15 | |||||||||||
Sponsor Name:F. HOFFMANN - LA ROCHE LTD. | |||||||||||||
Full Title: A phase II multicenter, randomized, double-blind, 12-week treatment, 3-arm, parallel-group, placebo-controlled study to investigate the efficacy, safety and tolerability of RO7017773 in participant... | |||||||||||||
Medical condition: Autism Spectrum Disorder (ASD) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003775-39 | Sponsor Protocol Number: F1D-MC_X311 | Start Date*: 2008-10-29 |
Sponsor Name:Charité – Universitätsmedizin Berlin | ||
Full Title: Randomised, placebo-controlled parallel-group trial to evaluate an oral dose of 10 mg Olanzapin combined with Riluzol for the treatment of appetite loss on patients with amyotrophic lateral sklerosis | ||
Medical condition: patients with amyotrophic lateral sclerosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2012-004263-47 | Sponsor Protocol Number: EMR200104-011 | Start Date*: 2013-03-01 | |||||||||||
Sponsor Name:Merck KGaA | |||||||||||||
Full Title: Open-label, single-arm, phase IV, multicenter trial to explore the immunogenicity of the liquid formulation of Saizen® in subjects with adult growth hormone deficiency (AGHD) of adult onset | |||||||||||||
Medical condition: Adult Growth Hormone Deficiency | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) SE (Completed) DE (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016921-32 | Sponsor Protocol Number: HSJD-OB-TRP | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Fundació Sant Joan de Déu | |||||||||||||
Full Title: A phase II, randomized, double-blind, placebo-controlled, in parallel groups clinical trial to assess the safety and efficacy of dietary supplementation with tryptophan to achieve weight loss, and ... | |||||||||||||
Medical condition: obesity | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004008-20 | Sponsor Protocol Number: IPI-145-06 | Start Date*: 2014-01-13 | |||||||||||
Sponsor Name:Verastem, Inc. | |||||||||||||
Full Title: A Phase 2 Study of IPI-145 in Subjects with Refractory Indolent Non-Hodgkin Lymphoma. | |||||||||||||
Medical condition: Refractory Indolent Non-Hodgkin Lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) IT (Completed) HU (Completed) CZ (Completed) ES (Completed) BE (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023534-23 | Sponsor Protocol Number: EMR 200061-504 | Start Date*: 2011-05-09 | ||||||||||||||||
Sponsor Name:Merck Serono S.A. - Geneva | ||||||||||||||||||
Full Title: A phase IIIB, multicentre, multinational, randomized, open-label trial to compare the efficacy and safety of ovarian stimulation with GONAL-f® day 1 to day 5 followed by Pergoveris® starting day 6 ... | ||||||||||||||||||
Medical condition: Fertility disorders | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: NL (Completed) SK (Completed) DE (Completed) FI (Completed) GB (Completed) DK (Completed) GR (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-002159-24 | Sponsor Protocol Number: 54861911ALZ2002 | Start Date*: 2014-10-27 | |||||||||||
Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
Full Title: A Phase 2a Randomized, Double-blind, Placebo-Controlled, Parallel-Group, Multi-center Study Investigating the Safety and Tolerability of JNJ-54861911 in Subjects in the Early (Predementia) Alzheime... | |||||||||||||
Medical condition: Early Alzheimer's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) SE (Completed) ES (Completed) NL (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000082-72 | Sponsor Protocol Number: RC-P0054 | Start Date*: 2019-01-03 | |||||||||||
Sponsor Name:Groupement des Hôpitaux de l'Institut Catholique de Lille (GHICL) | |||||||||||||
Full Title: Study of the communication of the hypothalamus with the periphery: impact of metformin on leptin transport in the cerebrospinal fluid of obese patients. A monocentric prospective study | |||||||||||||
Medical condition: OBESITY (BMI > 30) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003817-16 | Sponsor Protocol Number: EMR200061-005 | Start Date*: 2014-02-05 | |||||||||||
Sponsor Name:Merck KGaA | |||||||||||||
Full Title: A phase III, randomized, controlled, single-blind, multicentre, parallel arm trial to assess the efficacy and safety of Pergoveris® (follitropin alfa and lutropin alfa) and GONAL-f® (follitropin... | |||||||||||||
Medical condition: Poor Ovarian Response i.e. a failure to respond adequately to standard ART (assisted reproductive technologies) protocols and to recruit adequate follicles | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: CZ (Completed) SE (Completed) EE (Completed) HU (Completed) BE (Completed) GB (Completed) NL (Completed) DK (Completed) LV (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004634-26 | Sponsor Protocol Number: 4896 | Start Date*: 2015-05-20 | |||||||||||
Sponsor Name:Royal Liverpool University Hospital [...] | |||||||||||||
Full Title: The Effect of Live Attenuated Influenza Vaccine (LAIV) on Experimental Human Pneumococcal Colonisation (EHPC) Study | |||||||||||||
Medical condition: Pneumococcal colonisation post inoculation | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004920-40 | Sponsor Protocol Number: AFFECT | Start Date*: 2021-03-22 |
Sponsor Name:Vestre Viken HF | ||
Full Title: Affective effects of pre-surgery opioids (AFFECT): a randomized double-blind controlled trial | ||
Medical condition: Healthy adult surgery patients. Health status ASA1 or ASA2 as categorised by a medical doctor at the hospital based on medical history, physical examination. The American Society of Anesthesiologis... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NO (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-001254-29 | Sponsor Protocol Number: I2R-MC-BIAM | Start Date*: 2012-01-24 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: Protocol I2R-MC-BIAM The Impact of LY2605541 versus Insulin Glargine for Patients with Type 2 Diabetes Mellitus Advanced to Multiple Injection Bolus Insulin with Insulin Lispro: a Double-Blind, R... | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) SK (Completed) GB (Completed) CZ (Completed) AT (Completed) ES (Completed) LT (Completed) GR (Completed) IT (Completed) DK (Completed) NL (Completed) SI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021884-34 | Sponsor Protocol Number: PERS3 | Start Date*: 2013-01-24 | |||||||||||
Sponsor Name:Radboud University Medical Centre Nijmegen | |||||||||||||
Full Title: Relapse prevention in children and adolescents with DSM-IV Conduct Disorder treated with Risperidone: a Randomized Double blind, Placebo-Controlled, Discontinuation Study. | |||||||||||||
Medical condition: Conduct Disorder DSM-IV-TR; 312.8x, APA 2000 | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DE (Ongoing) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003159-12 | Sponsor Protocol Number: J4B-MC-OKAA | Start Date*: 2021-12-24 | |||||||||||
Sponsor Name:Prevail Therapeutics, a wholly-owned subsidiary of Eli Lilly and Company | |||||||||||||
Full Title: A Phase 1/2 Ascending Dose Study to Evaluate the Safety and Effects on Progranulin Levels of LY3884963 in Patients with Fronto-Temporal Dementia with Progranulin Mutations (FTD-GRN) (PROCLAIM) | |||||||||||||
Medical condition: Fronto-Temporal Dementia with Progranulin Mutations (FTD-GRN) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Trial now transitioned) ES (Temporarily Halted) FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-004648-27 | Sponsor Protocol Number: MS200569_0003 | Start Date*: 2022-03-21 | |||||||||||||||||||||
Sponsor Name:Merck Healthcare KGaA | |||||||||||||||||||||||
Full Title: A Phase II, Randomized, Double-Blind, Placebo Controlled Dose-Ranging, Parallel and Adaptive Study to Evaluate the Efficacy and Safety of Enpatoran in Systemic Lupus Erythematosus and in Cutaneous ... | |||||||||||||||||||||||
Medical condition: Systemic lupus erythematosus (SLE) and cutaneous lupus erythematosus (CLE) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Trial now transitioned) BG (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002527-21 | Sponsor Protocol Number: AMYPAD-01 | Start Date*: 2018-05-23 |
Sponsor Name:University of Geneva | ||
Full Title: Multicentre, Open-label, Randomised Study to Assess the Diagnostic Value of Amyloid PET Imaging in Patients with Subjective Cognitive Decline Plus, Mild Cognitive Impairment, or Dementia Where Alzh... | ||
Medical condition: Alzheimer's disease Mild Cognitive Impairment Subjective Cognitive Decline Plus | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) DE (Completed) ES (Ongoing) | ||
Trial results: (No results available) |
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