- Trials with a EudraCT protocol (124)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
124 result(s) found for: Adiposity.
Displaying page 4 of 7.
EudraCT Number: 2005-002364-29 | Sponsor Protocol Number: 015 | Start Date*: 2005-09-02 | |||||||||||
Sponsor Name: | |||||||||||||
Full Title: A Two Year Study to Assess the Efficacy, Safety, and Tolerability of MK-0364 in Obese Patients | |||||||||||||
Medical condition: Obesity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) NO (Prematurely Ended) DK (Prematurely Ended) CZ (Prematurely Ended) AT (Prematurely Ended) ES (Prematurely Ended) DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002454-21 | Sponsor Protocol Number: 014 | Start Date*: 2005-08-19 | |||||||||||
Sponsor Name:Merck Sharp & Dohme (Sweden) AB | |||||||||||||
Full Title: A 2-Year Study (1-Year Weight Loss Followed by 1-Year Prevention of Weight Regain) to Assess the Safety, Tolerability and Efficacy of Taranabant (MK-0364) in Obese Patients Followed by a 1-Year Ext... | |||||||||||||
Medical condition: Obesity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) GB (Prematurely Ended) IE (Completed) HU (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005192-18 | Sponsor Protocol Number: A5351022 | Start Date*: 2007-03-15 | |||||||||||
Sponsor Name:Pfizer Ltd. | |||||||||||||
Full Title: A 1-YEAR, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED PHASE 3 STUDY TO EVALUATE THE EFFICACY AND SAFETY OF CP-945,598 IN THE TREATMENT OF OVERWEIGHT, ORAL AGENT-TREATED SUBJECTS WITH TYPE 2 DIABET... | |||||||||||||
Medical condition: Obesity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) GB (Prematurely Ended) DE (Prematurely Ended) SK (Completed) SE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002199-88 | Sponsor Protocol Number: NN8022-1922 | Start Date*: 2008-12-15 | ||||||||||||||||
Sponsor Name:Novo Nordisk A/S | ||||||||||||||||||
Full Title: Effect of liraglutide on body weight in overweight or obese subjects with type 2 diabetes A 56 week randomised, double-blind, placebocontrolled, three armed parallel group, multi-centre, multina... | ||||||||||||||||||
Medical condition: Obesity and overweight | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) SE (Completed) ES (Completed) FR (Completed) GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-002479-37 | Sponsor Protocol Number: 1404-0036 | Start Date*: 2021-03-15 | |||||||||||
Sponsor Name:Boehringer Ingelheim AB | |||||||||||||
Full Title: A Phase II, randomized, double blind, parallel group,46 weeks dose-finding study of BI 456906 administered once weekly subcutaneously compared with placebo in patients with obesity or overweight | |||||||||||||
Medical condition: obesity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) IE (Prematurely Ended) NL (Completed) BE (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006175-36 | Sponsor Protocol Number: R256918OBE1008 | Start Date*: 2008-02-13 | |||||||||||
Sponsor Name:Janssen-Cilag International NV, Turnhoutseweg 30, 2340 Beerse, Belgium | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Study to Evaluate the Effect of JNJ-16269110 on Hepatic Triglyceride Content in Obese Subjects | |||||||||||||
Medical condition: Obesity | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) NL (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000546-34 | Sponsor Protocol Number: NN8022-4392 | Start Date*: 2021-02-10 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: Effect and safety of liraglutide 3.0 mg on weight management in children with obesity aged 6 to <12 years: 56-week, double-blind, randomised, placebo-controlled trial | |||||||||||||
Medical condition: Obesity | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Trial now transitioned) PT (Trial now transitioned) NO (Not Authorised) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001247-27 | Sponsor Protocol Number: 202100166 | Start Date*: 2021-09-30 | ||||||||||||||||
Sponsor Name:University Medical Center Groningen | ||||||||||||||||||
Full Title: SeMaglutide and Albuminuria Reduction Trial in obese individuals without diabetes | ||||||||||||||||||
Medical condition: Overweight and obese individuals at high risk of chronic kidney disease progression. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) DE (Completed) ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002939-29 | Sponsor Protocol Number: NN9536-4734 | Start Date*: 2021-07-05 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: Efficacy and safety of subcutaneous semaglutide 2.4 mg once-weekly in subjects with obesity and prediabetes | |||||||||||||
Medical condition: Obesity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) DK (Completed) ES (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003380-35 | Sponsor Protocol Number: EX9536-4388 | Start Date*: 2018-10-05 | ||||||||||||||||
Sponsor Name:Novo Nordisk A/S | ||||||||||||||||||
Full Title: SELECT - Semaglutide effects on cardiovascular outcomes in people with overweight or obesity | ||||||||||||||||||
Medical condition: Overweight Obesity | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BG (Completed) DK (Completed) FI (Completed) IE (Completed) PT (Completed) GB (GB - no longer in EU/EEA) LV (Completed) NL (Completed) CZ (Completed) HU (Completed) BE (Completed) AT (Completed) SE (Completed) HR (Completed) NO (Completed) IT (Completed) RO (Ongoing) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-000790-94 | Sponsor Protocol Number: NN9536-4999 | Start Date*: 2022-11-07 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: Effect and safety of semaglutide 7.2 mg once-weekly in participants with obesity. | |||||||||||||
Medical condition: Obesity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) PT (Completed) NO (Completed) SK (Completed) HU (Completed) BG (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000703-15 | Sponsor Protocol Number: A5351028 | Start Date*: 2007-06-19 | |||||||||||
Sponsor Name:Pfizer Inc, 235 East 42nd Street, New York, NY 10017, United States | |||||||||||||
Full Title: A 15 MONTH, RANDOMIZED, DOUBLE BLIND, PLACEBO CONTROLLED PHASE 3 STUDY TO EVALUATE THE LONG TERM EFFICACY AND SAFETY OF CP 945,598 IN PREVENTION OF WEIGHT REGAIN IN OBESE SUBJECTS | |||||||||||||
Medical condition: Obesity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003616-39 | Sponsor Protocol Number: 64565111OBE2001 | Start Date*: 2018-04-27 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Randomized, Double-blind Placebo-controlled and Open-label Active-controlled, Parallel-group, Multicenter, Dose-ranging Study to Evaluate the Safety and Efficacy of JNJ-64565111 in Non-diabetic S... | |||||||||||||
Medical condition: Obesity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) BE (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002422-78 | Sponsor Protocol Number: 1 | Start Date*: 2013-10-14 | |||||||||||
Sponsor Name:University of Leicester | |||||||||||||
Full Title: Impact of liraglutide on cardiac function and structure in young adults with type 2 diabetes: an open lable, randomised active-comparator trial. | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002076-41 | Sponsor Protocol Number: 0667 | Start Date*: 2018-08-23 | ||||||||||||||||
Sponsor Name:University of Leicester | ||||||||||||||||||
Full Title: A RANDOMISED CONTROLLED TRIAL OF PRE-SURGERY SODIUM VALPROATE, FOR THE PREVENTION OF ORGAN INJURY IN CARDIAC SURGERY: Val-CARD | ||||||||||||||||||
Medical condition: Reduction of myocardial and kidney injury risk of post cardiac surgery by increasing the expression of genes that promote myocardial mitochondrial homeostasis via effects on chromatin histone deace... | ||||||||||||||||||
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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) |
EudraCT Number: 2012-004988-42 | Sponsor Protocol Number: 12DIAB15 | Start Date*: 2013-02-05 | ||||||||||||||||
Sponsor Name:Sandwell and West Birmingham Hospitals NHS Trust | ||||||||||||||||||
Full Title: REVISE-Diabesity: Randomisation to Endoluminal intestinal liner alone Versus with Incretin analogue in SustainEd Diabesity | ||||||||||||||||||
Medical condition: Combined Type 2 diabetes mellitus and obesity. | ||||||||||||||||||
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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) |
EudraCT Number: 2015-000060-34 | Sponsor Protocol Number: LOCAL/2015/APM-01 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:CHU de Nîmes | |||||||||||||
Full Title: Effets vasculaires et métaboliques d'une supplémentation en Vitamine D associée à une prise en charge hygiéno-diététique chez l'Adolescent Obèse: étude prospective, randomisée, contrôlée | |||||||||||||
Medical condition: Obésité chez l'adolescent | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001145-93 | Sponsor Protocol Number: 69HCL15_0057 | Start Date*: 2015-10-07 | ||||||||||||||||
Sponsor Name:Hospices Civils de Lyon | ||||||||||||||||||
Full Title: Étude pharmacocinétique de la lidocaïne par voie intraveineuse en chirurgie bariatrique - Etude SPIRAL (Safety Profile of IntRAvenous Lidocaïne use in coelioscopic bariatric surgery) | ||||||||||||||||||
Medical condition: Obésité / Chirurgie bariatrique | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016663-11 | Sponsor Protocol Number: ORA111850 | Start Date*: 2010-08-27 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: A 35-Day, Multi-Centre, Randomised, Parallel-Group, Double-Blind, Placebo-Controlled Proof of Concept Study to Investigate the Effects of GSK1521498 on Body Weight and Composition, Eating Behaviour... | |||||||||||||
Medical condition: GSK1521498 is a novel opioid receptor inverse agonist that is being developed for the treatment of obesity. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022815-21 | Sponsor Protocol Number: FARM87JEA3 | Start Date*: 2010-12-16 | ||||||||||||||||||||||||||
Sponsor Name:UNIVERSITA` DI TORINO | ||||||||||||||||||||||||||||
Full Title: Use of metformin in obese adolescent patients | ||||||||||||||||||||||||||||
Medical condition: Obesity | ||||||||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
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