interventional clinical trials that were approved in the European Union (EU)/European Economic Area (EEA) under the Clinical Trials Directive 2001/20/EC
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44335
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are clinical trials conducted with subjects less than 18 years old.
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18700
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5 result(s) found for: Melanocortin 3 receptor.
Displaying page 1 of 1.
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:(No results available)
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
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 Leptin Receptor (LEPR) Deficiency...
Medical condition: Early Onset Leptin Receptor (LEPR) Deficiency Obesity due to Bi-Allelic Loss-of-Function LEPR Genetic Mutation
Disease:
Population Age: Children, Adolescents, Under 18, Adults
Full Title: Setmelanotide (RM-493) Treatment Trial in Patients with rare genetic disorders of obesity
Medical condition: Body weight is regulated within the hypothalamus. In rare cases mutations in genes, which are embedded in the signaling cascades of the hypothalamus lead to early onset severe obesity. POMC is one ...
Full Title: A Phase 3, Randomized, Double-Blind Trial of Two Formulations of Setmelanotide (Daily and Weekly) with a Crossover to Open-Label Once Weekly Setmelanotide in Patients with Specific Gene Defects in ...
Medical condition: Treatment of obesity associated with genetic defects upstream of the MC4 receptor in the leptin-melanocortin pathway. Diseases that are the result of genetic defects affecting the MC4R pathway, con...
Disease:
Version
SOC Term
Classification Code
Term
Level
23.0
10010331 - Congenital, familial and genetic disorders
10084105
Leptin receptor deficiency
PT
23.0
10010331 - Congenital, familial and genetic disorders
10083937
Pro-opiomelanocortin deficiency
PT
20.1
10010331 - Congenital, familial and genetic disorders
10048680
Bardet-Biedl syndrome
LLT
Population Age: Children, Adolescents, Under 18, Adults
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