- Trials with a EudraCT protocol (49)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
49 result(s) found for: Hunger.
Displaying page 1 of 3.
| EudraCT Number: 2013-004411-53 | Sponsor Protocol Number: Erythromycin_v5 | Start Date*: 2014-05-15 |
| Sponsor Name:University of Leuven | ||
| Full Title: Brain mechanisms underlying the effect of the motilin receptor agonist erythromycin on hunger in normal weight subjects | ||
| Medical condition: The effect of erythromycin administration on hunger and brain responses will be tested in healthy volunteers | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-001949-13 | Sponsor Protocol Number: LIRHV | Start Date*: 2019-01-31 | |||||||||||
| Sponsor Name:KU Leuven | |||||||||||||
| Full Title: The effect of liraglutide on MMC activity, gastrointestinal hormones, hunger ratings and ad libitum food intake in healthy volunteers | |||||||||||||
| Medical condition: The study will focus on the underlying mechanisms of obesity. The effects will first be investigated in healthy, lean volunteers. | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-004082-33 | Sponsor Protocol Number: erythstom2 | Start Date*: 2011-10-05 |
| Sponsor Name:UZLeuven | ||
| Full Title: The role of induced phase 3 contractions in the control of hunger and food intake | ||
| Medical condition: Gastrointestinal contractility will be studied in healthy volunteers for 7 hours in a fasting condition | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-004600-35 | Sponsor Protocol Number: Modifast3 | Start Date*: 2012-12-19 |
| Sponsor Name:KULeuven | ||
| Full Title: Effect of diet-induced weight loss on motilin, ghrelin, bitter taste perception, hunger and the migrating motor complex: a prospective study | ||
| Medical condition: Gastrointestinal contractility and hormones will be studied in obese patients before and after weight loss induced by a diet | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-004946-41 | Sponsor Protocol Number: s57223 | Start Date*: 2014-11-19 |
| Sponsor Name:KULeuven | ||
| Full Title: The influence of GLP-1 analog, liraglutide, on gastric accommodation, gastric emptying, hunger and the migrating motor complex in healthy volunteers | ||
| Medical condition: healthy volunteers no medical condition; drug will be studied because it is known to influence gastric motility | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-004978-95 | Sponsor Protocol Number: VildaMMC | Start Date*: 2014-03-12 |
| Sponsor Name:KULeuven | ||
| Full Title: the influence of a DPP-4 inhibitor, vildaglitpin, on hunger and the migrating motor complex in healthy volunteers | ||
| Medical condition: healthy volunteers no medical condition, drug will be studied because they are known to influence gastric motility | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-007970-47 | Sponsor Protocol Number: fMRI-Ex-4 | Start Date*: Information not available in EudraCT | ||||||||||||||||
| Sponsor Name:University of Leipzig | ||||||||||||||||||
| Full Title: Central nervous effects of exendin-4 on hunger and satiety in obesity and diabetes mellitus type 2: an fMRI study | ||||||||||||||||||
| Medical condition: Obesity (N=20) vs. obesity with type 2 diabetes (N=20); Randomised + controlled + cross-over + prospective + double-blind + stratified + 2 arms: Exendin-4 vs NaCl 0.9% iv ober 100 minutes on two s... | ||||||||||||||||||
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| Population Age: Adults | Gender: Male | |||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2021-002855-12 | Sponsor Protocol Number: RM-493-034 | Start Date*: 2022-04-22 |
| Sponsor Name:Rhythm Pharmaceuticals Inc. | ||
| Full Title: A 2-Stage (Open-Label Run-in followed by Randomized Withdrawal), Double-Blind, Placebo-Controlled, Phase 2 study of Setmelanotide in Patients with Specific Gene Defects in the Melanocortin-4 Rece... | ||
| Medical condition: Specific Gene Defects in the Melanocortin-4 Receptor Pathway, responsible for improper functions of certain messenger materials in the body. E.g Melanocyte-Stimulating Hormone (MSH) | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: FR (Completed) DE (Completed) ES (Ongoing) NL (Completed) GR (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2022-004107-32 | Sponsor Protocol Number: RM-493-030 | Start Date*: 2023-01-23 |
| Sponsor Name:Rhythm Pharmaceuticals, Inc. | ||
| Full Title: A Phase 2, Open-Label 20-Week Study to Evaluate the Safety and Efficacy of Setmelanotide in Subjects with Hypothalamic Obesity | ||
| Medical condition: Hypothalamic Obesity | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2016-002320-83 | Sponsor Protocol Number: RM-493-012 | Start Date*: 2016-09-28 |
| Sponsor Name:Rhythm Pharmaceuticals, Inc. | ||
| Full Title: An Open Label, 1-Year Trial, including a Double-Blind Placebo-Controlled Withdrawal Period, of Setmelanotide (RM-493), a Melanocortin 4 Receptor (MC4R) Agonist, in Early Onset POMC Deficiency Obesi... | ||
| Medical condition: Early onset pro-opiomelanocortin deficiency obesity | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) GB (Completed) FR (Completed) BE (Completed) ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-005006-35 | Sponsor Protocol Number: RM-493-022 | Start Date*: 2018-05-30 |
| Sponsor Name:Rhythm Pharmaceuticals, Inc. | ||
| Full Title: Long Term Extension Trial of setmelanotide (RM-493) for patients who have completed a trial of Setmelanotide for the treatment of obesity associated with genetic defects upstream of the MC4 recepto... | ||
| Medical condition: Patients with obesity caused by genetic defects upstream of the MC4 receptor in the leptin-melanocortin pathway. Human Genetics studies have identified several diseases that are the result of genet... | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) FR (Completed) NL (Completed) GB (GB - no longer in EU/EEA) BE (Completed) ES (Completed) GR (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-003083-30 | Sponsor Protocol Number: PLAQHV | Start Date*: 2019-01-31 | |||||||||||
| Sponsor Name:UZ Leuven | |||||||||||||
| Full Title: The effect of hydroxychloroquine sulphate on hedonic food intake, appetite-related sensations and gastrointestinal hormone release in healthy female subjects | |||||||||||||
| Medical condition: The study is meant to have a better understanding in obesity and how we can prevent/cure it. Therefore, the product will first be tested in healthy, lean volunteers. | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-003107-65 | Sponsor Protocol Number: OPNT001-BN-001 | Start Date*: 2017-01-11 | |||||||||||
| Sponsor Name:Opiant Pharmaceuticals Inc | |||||||||||||
| Full Title: Randomised, double-blind, placebo controlled trial evaluating the effects of naloxone hydrochloride nasal spray on eating behaviours in bulimia nervosa | |||||||||||||
| Medical condition: Bulimia nervosa | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-000387-14 | Sponsor Protocol Number: RM-493-014 | Start Date*: 2017-05-24 |
| Sponsor Name:Rhythm Pharmaceuticals, Inc. | ||
| Full Title: Setmelanotide (RM-493) Phase 2 Treatment Trial in Patients with rare genetic disorders of obesity | ||
| Medical condition: - POMC/PCSK1/LEPR heterozygous - POMC/PCSK1/LEPR compound heterozygous or homozygous deficiency obesity - POMC/PCSK1/LEPR composite heterozygous deficiency obesity - Smith-Magenis Syndrome - SH2B1... | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) ES (Ongoing) DE (Completed) FR (Ongoing) NL (Completed) GR (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2004-003887-31 | Sponsor Protocol Number: 2004/116 | Start Date*: 2004-12-09 |
| Sponsor Name:Klinisk Farmakologisk Center og Med. Afd. M, Århus Sygehus, NBG | ||
| Full Title: "Farmakodynamiske egenskaber af to langtidsvirkende insulinanaloger i sammenligning med NPH insulin" | ||
| Medical condition: Healthy subjects. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male | |
| Trial protocol: DK (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-004381-18 | Sponsor Protocol Number: 2012/1226 | Start Date*: 2013-06-04 |
| Sponsor Name:St Olavs Hospital Trondheim University Hospital | ||
| Full Title: Treatment of morbid obesity through intra-gastric injections of Botulinum toxin A: A pilot study | ||
| Medical condition: Morbid obesity (obesity class 3) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NO (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-004058-11 | Sponsor Protocol Number: RM-493-023 | Start Date*: Information not available in EudraCT |
| Sponsor Name:Rhythm Pharmaceuticals, Inc. | ||
| Full Title: A Phase 3 trial of Setmelanotide (RM-493), a Melanocortin-4 Receptor (MC4R) Agonist, in Bardet-Biedl Syndrome (BBS) and Alström syndrome (AS) Patients with Moderate to Severe Obesity | ||
| Medical condition: Obesity and hyperphagia in patients with Bardet-Biedl Syndrome or Alström syndrome | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: FR (Completed) ES (Completed) GB (GB - no longer in EU/EEA) | ||
| Trial results: View results | ||
| EudraCT Number: 2021-002873-24 | Sponsor Protocol Number: RM-493-035 | Start Date*: 2022-05-16 |
| Sponsor Name:Rhythm Pharmaceuticals Inc. | ||
| Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study: 5 Independent Sub-studies of Setmelanotide in Patients with POMC, PCSK1, LEPR, SRC1, SH2B1, and PCSK1 N221D Gene Defects in the Melano... | ||
| Medical condition: Specific Gene Defects in the Melanocortin-4 Receptor Pathway, responsible for improper functions of certain messenger materials in the body. E.g Melanocyte-Stimulating Hormone (MSH) | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) ES (Ongoing) DE (Trial now transitioned) GR (Trial now transitioned) NL (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-000753-24 | Sponsor Protocol Number: DC2011LiBrain001 | Start Date*: 2011-10-13 | ||||||||||||||||
| Sponsor Name:VU University Medical Center | ||||||||||||||||||
| Full Title: Central effects of endogenous GLP-1 and the GLP-1 analog liraglutide on brain satiety and reward circuits and feeding behavior in diabetes. | ||||||||||||||||||
| Medical condition: diabetes mellitus obesity | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2010-022334-92 | Sponsor Protocol Number: qmul250510 | Start Date*: 2011-01-07 |
| Sponsor Name:Barts and the London School of Medicine and Dentistry, Queen Mary University of London | ||
| Full Title: Effects of a combination of varenicline and transdermal nicotine patch on post-quitting urges to smoke | ||
| Medical condition: Tobacco dependence (smoking cessation) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
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